Page last updated: 2024-08-03 15:33:14

cp 466722

Description

2-(6,7-dimethoxy-4-quinazolinyl)-5-(2-pyridinyl)-1,2,4-triazol-3-amine : no description available [CHeBI]

Cross-References

ID SourceID
PubMed CID44551660
CHEMBL ID2143829
SCHEMBL ID15639218
CHEBI ID91330
MeSH IDM0525865

Synonyms (41)

Synonym
HY-11002
chembl2143829 ,
bdbm50145038
1080622-86-1
BCP9000544
CP-466722 ,
cp 466722
cp466722
HMS3265B19
HMS3265B20
HMS3265A20 ,
HMS3265A19
NCGC00263099-01
S2245
2-(6,7-dimethoxyquinazolin-4-yl)-5-(pyridin-2-yl)-2h-1,2,4-triazol-3-amine
1-(6,7-dimethoxy-4-quinazolinyl)-3-(2-pyridinyl)-1h-1,2,4-triazol-5-amine
BRD-K15592317-001-01-0
J-503445
2-(6,7-dimethoxy-quinazolin-4-yl)-5-pyridin-2-yl-2h-[1,2,4]triazol-3-ylamine
SCHEMBL15639218
gtpl9359
1-(6,7-dimethoxyquinazolin-4-yl)-3-(pyridin-2-yl)-1h-1,2,4-triazol-5-amine
AC-28457
2-(6,7-dimethoxyquinazolin-4-yl)-5-pyridin-2-yl-1,2,4-triazol-3-amine
DTXSID80659313
EX-A086
AKOS027422720
CHEBI:91330
cp466722, >=98% (hplc)
mfcd17392566
NCGC00263099-05
2-(6,7-dimethoxy-4-quinazolinyl)-5-(2-pyridinyl)-1,2,4-triazol-3-amine
Q27163212
BCP02229
SB19278
NCGC00263099-08
A25042
2-(6,7-dimethoxyquinazolin-4-yl)-5-(pyridin-2-yl)-2h-1,2,4-triazol-3-amine;cp-466722
NCGC00263099-02
AS-78299
Z2036684827

Drug Classes (1)

ClassDescription
quinazolinesAny organic heterobicyclic compound based on a quinazoline skeleton and its substituted derivatives.

Protein Targets (17)

Potency Measurements

ProteinTaxonomyMeasurementAverage (mM)Bioassay(s)
PPM1D proteinHomo sapiens (human)Potency2.9411AID1347411
cytochrome P450 family 3 subfamily A polypeptide 4Homo sapiens (human)Potency23.9185AID1645841
EWS/FLI fusion proteinHomo sapiens (human)Potency14.2231AID1259252; AID1259253; AID1259255; AID1259256
GVesicular stomatitis virusPotency8.4866AID1645842
cytochrome P450 2D6Homo sapiens (human)Potency7.5637AID1645840
tyrosine-protein kinase YesHomo sapiens (human)Potency2.7404AID686947
Interferon betaHomo sapiens (human)Potency4.3275AID1347411; AID1645842
HLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)Potency8.4866AID1645842
Inositol hexakisphosphate kinase 1Homo sapiens (human)Potency8.4866AID1645842
cytochrome P450 2C9, partialHomo sapiens (human)Potency8.4866AID1645842

Inhibition Measurements

ProteinTaxonomyMeasurementAverage (mM)Bioassay(s)
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoformHomo sapiens (human)IC501.4900AID1635548
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit beta isoformHomo sapiens (human)IC505.4400AID1635549
Serine/threonine-protein kinase mTORHomo sapiens (human)IC504.5900AID1635546
Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform Homo sapiens (human)IC501.0000AID1635550
DNA-dependent protein kinase catalytic subunitHomo sapiens (human)IC500.8790AID1635547
Serine-protein kinase ATMHomo sapiens (human)IC500.6748AID1276244; AID1276306; AID1635523; AID1635524; AID1687210; AID1743714; AID1903635
Serine/threonine-protein kinase ATRHomo sapiens (human)IC5030.0000AID1635525

Bioassays (85)

Assay IDTitleYearJournalArticle
AID1296008Cytotoxic Profiling of Annotated Libraries Using Quantitative High-Throughput Screening2020SLAS discovery : advancing life sciences R & D, 01, Volume: 25, Issue:1
ISSN: 2472-5560
Cytotoxic Profiling of Annotated and Diverse Chemical Libraries Using Quantitative High-Throughput Screening.
AID1346987P-glycoprotein substrates identified in KB-8-5-11 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
ISSN: 1521-0111
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
AID1346986P-glycoprotein substrates identified in KB-3-1 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
ISSN: 1521-0111
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
AID1347159Primary screen GU Rhodamine qHTS for Zika virus inhibitors: Unlinked NS2B-NS3 protease assay2020Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
ISSN: 1091-6490
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
AID1347160Primary screen NINDS Rhodamine qHTS for Zika virus inhibitors2020Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
ISSN: 1091-6490
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
AID1347106qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for control Hh wild type fibroblast cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
ISSN: 1949-2553
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347094qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for BT-37 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
ISSN: 1949-2553
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347103qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for OHS-50 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
ISSN: 1949-2553
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347099qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for NB1643 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
ISSN: 1949-2553
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347083qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lassa (LASV) Arenavirus: Viability assay - alamar blue signal for LASV Primary Screen2020Antiviral research, 01, Volume: 173ISSN: 1872-9096A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID1347092qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for A673 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
ISSN: 1949-2553
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347108qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Rh41 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
ISSN: 1949-2553
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347105qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for MG 63 (6-TG R) cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
ISSN: 1949-2553
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347100qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for LAN-5 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
ISSN: 1949-2553
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID686947qHTS for small molecule inhibitors of Yes1 kinase: Primary Screen2013Bioorganic & medicinal chemistry letters, Aug-01, Volume: 23, Issue:15
ISSN: 1464-3405
Identification of potent Yes1 kinase inhibitors using a library screening approach.
AID1745845Primary qHTS for Inhibitors of ATXN expression2022The Journal of biological chemistry, 08, Volume: 298, Issue:8
ISSN: 1083-351X
AID1347095qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for NB-EBc1 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
ISSN: 1949-2553
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347082qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lassa (LASV) Arenavirus: LASV Primary Screen - GLuc reporter signal2020Antiviral research, 01, Volume: 173ISSN: 1872-9096A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID1347107qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Rh30 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
ISSN: 1949-2553
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347098qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SK-N-SH cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
ISSN: 1949-2553
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347091qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SJ-GBM2 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
ISSN: 1949-2553
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347154Primary screen GU AMC qHTS for Zika virus inhibitors2020Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
ISSN: 1091-6490
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
AID1347086qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lymphocytic Choriomeningitis Arenaviruses (LCMV): LCMV Primary Screen - GLuc reporter signal2020Antiviral research, 01, Volume: 173ISSN: 1872-9096A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID1508630Primary qHTS for small molecule stabilizers of the endoplasmic reticulum resident proteome: Secreted ER Calcium Modulated Protein (SERCaMP) assay2021Cell reports, 04-27, Volume: 35, Issue:4
ISSN: 2211-1247
A target-agnostic screen identifies approved drugs to stabilize the endoplasmic reticulum-resident proteome.
AID1347101qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for BT-12 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
ISSN: 1949-2553
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347093qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SK-N-MC cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
ISSN: 1949-2553
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347096qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for U-2 OS cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
ISSN: 1949-2553
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347104qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for RD cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
ISSN: 1949-2553
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347089qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for TC32 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
ISSN: 1949-2553
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347102qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Rh18 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
ISSN: 1949-2553
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347097qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for Saos-2 cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
ISSN: 1949-2553
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1347090qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for DAOY cells2018Oncotarget, Jan-12, Volume: 9, Issue:4
ISSN: 1949-2553
Quantitative high-throughput phenotypic screening of pediatric cancer cell lines identifies multiple opportunities for drug repurposing.
AID1276260Plasma protein binding in rat2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276263Stability of the compound in phosphate buffered saline assessed as compound stability time at pH 7.4 by UPLC-MS analysis2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276267Half life of the compound in aqueous buffer2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276249Half life in rat liver microsomes by UPLC-MS analysis2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276271Inhibition of ATM in human MCF7 cells assessed as inhibition of KAP1 phosphorylation at Ser824 residue preincubated for 30 mins followed cells exposed to 10 Gy irradiation measured after 1 hr by western blot analysis2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276255Intrinsic clearance in dog liver microsomes after 0.5 to 4 hrs by UPLC-MS analysis2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276274Sensitization of infrared-induced DNA damage in human MCF7 cells assessed as reduction in colony formation at 10 uM pretreated for 10 mins followed by irradiation for 4 hrs measured after 10 days by crystal violet staining analysis2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276245Solubility of the compound in PBS at pH 7.4 for 18 hrs by UV spectroscopic analysis2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276250Half life in human liver microsomes by UPLC-MS analysis2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276252Intrinsic clearance in CD-1 mouse liver microsomes after 0.5 to 4 hrs by UPLC-MS analysis2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1635523Inhibition of ATM (unknown origin) using p53 as substrate incubated for 30 mins followed by substrate addition measured after 2 hrs in presence of ATP by HTRF method2016Journal of medicinal chemistry, 07-14, Volume: 59, Issue:13
ISSN: 1520-4804
Discovery of Novel 3-Quinoline Carboxamides as Potent, Selective, and Orally Bioavailable Inhibitors of Ataxia Telangiectasia Mutated (ATM) Kinase.
AID1276302Half life in C57BL/6 mouse at 10 mg/kg, iv2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1903635Competitive inhibition of ATM (unknown origin) measured by ATP-competitive binding assay2022European journal of medicinal chemistry, Apr-05, Volume: 233ISSN: 1768-3254Discovery of novel ataxia telangiectasia mutated (ATM) kinase modulators: Computational simulation, biological evaluation and cancer combinational chemotherapy study.
AID1276265Stability of the compound in phosphate buffered saline assessed as compound stability time at pH 3 by UPLC-MS analysis2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276247Permeability of the compound at 10 uM after 30 mins by PAMPA2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276306Inhibition of flag-tagged ATM (unknown origin) using p53 as substrate by ELISA2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1635525Inhibition of ATR in human HT-29 cells assessed as reduction in Chk1 phosphorylation at Ser-345 residue after 60 mins in presence of 4-nitroquinoline-1-oxide by Hoechst 33258 staining based plate reader analysis2016Journal of medicinal chemistry, 07-14, Volume: 59, Issue:13
ISSN: 1520-4804
Discovery of Novel 3-Quinoline Carboxamides as Potent, Selective, and Orally Bioavailable Inhibitors of Ataxia Telangiectasia Mutated (ATM) Kinase.
AID1276246Cytotoxicity against human BJ cells after 72 hrs by Cell Titer Glo assay2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276254Intrinsic clearance in human liver microsomes after 0.5 to 4 hrs by UPLC-MS analysis2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276256Stability in mouse plasma assessed as compound stability time by UPLC-MS analysis2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1743714Inhibition of full length Flag-tagged ATM (unknown origin) using GST-p53(1 to 101 residues) as substrates incubated for 90 mins2020Journal of medicinal chemistry, 12-10, Volume: 63, Issue:23
ISSN: 1520-4804
Synthetic Lethality through the Lens of Medicinal Chemistry.
AID1276262Plasma protein binding in dog2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276272Inhibition of ATM in human MCF7 cells assessed as inhibition of p53 phosphorylation at Ser15 residue preincubated for 30 mins followed cells exposed to 10 Gy irradiation measured after 1 hr by western blot analysis2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276295Drug metabolism in C57BL/6 mouse assessed as 4-(5-amino-3-(pyridin-2-yl)-1H-1,2,4-triazol-1-yl)quinazoline-6,7,8-triol formation by qualitative tandem mass spectrometric analysis2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1687210Inhibition of ATM in human MCF7 cells assessed as reduction in KAP1 phosphorylation2019Journal of medicinal chemistry, 03-28, Volume: 62, Issue:6
ISSN: 1520-4804
Optimization of Potent and Selective Ataxia Telangiectasia-Mutated Inhibitors Suitable for a Proof-of-Concept Study in Huntington's Disease Models.
AID1276261Plasma protein binding in human2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1635549Inhibition of human recombinant PI3Kbeta using PIP2/ATP as substrate incubated for 20 mins followed by substrate addition by Kinase Glo reagent based luminescence assay2016Journal of medicinal chemistry, 07-14, Volume: 59, Issue:13
ISSN: 1520-4804
Discovery of Novel 3-Quinoline Carboxamides as Potent, Selective, and Orally Bioavailable Inhibitors of Ataxia Telangiectasia Mutated (ATM) Kinase.
AID1635524Inhibition of ATM phosphorylation at Ser-1981 residue in human HT-29 cells incubated for 1 hr followed by X-ray irradiation by Hoechst staining based fluorescence plate reader analysis2016Journal of medicinal chemistry, 07-14, Volume: 59, Issue:13
ISSN: 1520-4804
Discovery of Novel 3-Quinoline Carboxamides as Potent, Selective, and Orally Bioavailable Inhibitors of Ataxia Telangiectasia Mutated (ATM) Kinase.
AID1635550Inhibition of human recombinant PI3Kgamma using PIP2/ATP as substrate incubated for 20 mins followed by substrate addition by Kinase Glo reagent based luminescence assay2016Journal of medicinal chemistry, 07-14, Volume: 59, Issue:13
ISSN: 1520-4804
Discovery of Novel 3-Quinoline Carboxamides as Potent, Selective, and Orally Bioavailable Inhibitors of Ataxia Telangiectasia Mutated (ATM) Kinase.
AID1276300Toxicity in C57BL/6 mouse at 10 and 20 mg/kg, iv2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276270Inhibition of ATM in human MCF7 cells assessed as inhibition of enzyme phosphorylation at Ser1981 residue preincubated for 30 mins followed cells exposed to 10 Gy irradiation measured after 1 hr by western blot analysis2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276257Stability in rat plasma assessed as compound stability time by UPLC-MS analysis2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276296Drug metabolism in C57BL/6 mouse assessed as (2S,3S,4S,5R,6S)-6-(4-(5-amino-3-(pyridin-2-yl)-1H-1,2,4-triazol-1-yl)-7-methoxyquinazolin-6-yloxy)-3,4,5-trihydroxytetrahydro-2H-pyran-2-carboxylic acid formation by qualitative tandem mass spectrometric analy2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276244Inhibition of ATM kinase in human MCF7 cells after 1 hr by immunofluorescence assay2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1635546Inhibition of C-terminal FLAG-tagged recombinant mTOR (1362 to 2549 residues) (unknown origin) using Biotin-Ahx-Lys-Lys-Ala-Asn-Gln-Val-Phe-Leu-Gly-Phe-Thr-Tyr-Val-Ala-Pro-Ser-Val-Leu-Glu-Ser-Val-Lys-Glu-NH2 as substrate after 90 mins by AlphaScreen assay2016Journal of medicinal chemistry, 07-14, Volume: 59, Issue:13
ISSN: 1520-4804
Discovery of Novel 3-Quinoline Carboxamides as Potent, Selective, and Orally Bioavailable Inhibitors of Ataxia Telangiectasia Mutated (ATM) Kinase.
AID1276251Half life in dog liver microsomes by UPLC-MS analysis2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1635527Intrinsic clearance in rat hepatocytes assessed per million cells measured up to 90 mins2016Journal of medicinal chemistry, 07-14, Volume: 59, Issue:13
ISSN: 1520-4804
Discovery of Novel 3-Quinoline Carboxamides as Potent, Selective, and Orally Bioavailable Inhibitors of Ataxia Telangiectasia Mutated (ATM) Kinase.
AID1635530Buffer/octanol partition coefficient, log D of the compound at pH 7.4 by shake flask method2016Journal of medicinal chemistry, 07-14, Volume: 59, Issue:13
ISSN: 1520-4804
Discovery of Novel 3-Quinoline Carboxamides as Potent, Selective, and Orally Bioavailable Inhibitors of Ataxia Telangiectasia Mutated (ATM) Kinase.
AID1276292Tmax in C57BL/6 mouse at 20 mg/kg, iv by UPLC-MS analysis2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276301Clearance in C57BL/6 mouse at 10 mg/kg, iv2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276268Cmax in C57BL/6 mouse at 20 mg/kg, iv by UPLC-MS analysis2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276253Intrinsic clearance in rat liver microsomes after 0.5 to 4 hrs by UPLC-MS analysis2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276258Plasma protein binding in mouse2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276264Stability of the compound in phosphate buffered saline assessed as compound stability time at pH 5 by UPLC-MS analysis2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276293Drug metabolism in C57BL/6 mouse assessed as 4-(5-amino-3-(pyridin-2-yl)-1H-1,2,4-triazol-1-yl)-7-methoxyquinazolin-6-ol formation by qualitative tandem mass spectrometric analysis2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1635547Inhibition of DNAPK (unknown origin) using p53-based peptide substrate preincubated for 5 min prior to ATP addition2016Journal of medicinal chemistry, 07-14, Volume: 59, Issue:13
ISSN: 1520-4804
Discovery of Novel 3-Quinoline Carboxamides as Potent, Selective, and Orally Bioavailable Inhibitors of Ataxia Telangiectasia Mutated (ATM) Kinase.
AID1276248Half life in CD-1 mouse liver microsomes by UPLC-MS analysis2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1276259Stability in human plasma assessed as compound stability time by UPLC-MS analysis2016Journal of medicinal chemistry, Jan-28, Volume: 59, Issue:2
ISSN: 1520-4804
Optimization of a Novel Series of Ataxia-Telangiectasia Mutated Kinase Inhibitors as Potential Radiosensitizing Agents.
AID1635548Inhibition of human recombinant PI3Kalpha using PIP2/ATP as substrate incubated for 20 mins followed by substrate addition by Kinase Glo reagent based luminescence assay2016Journal of medicinal chemistry, 07-14, Volume: 59, Issue:13
ISSN: 1520-4804
Discovery of Novel 3-Quinoline Carboxamides as Potent, Selective, and Orally Bioavailable Inhibitors of Ataxia Telangiectasia Mutated (ATM) Kinase.
AID1635526Intrinsic clearance in human hepatocytes assessed per million cells measured up to 90 mins2016Journal of medicinal chemistry, 07-14, Volume: 59, Issue:13
ISSN: 1520-4804
Discovery of Novel 3-Quinoline Carboxamides as Potent, Selective, and Orally Bioavailable Inhibitors of Ataxia Telangiectasia Mutated (ATM) Kinase.
AID1347411qHTS to identify inhibitors of the type 1 interferon - major histocompatibility complex class I in skeletal muscle: primary screen against the NCATS Mechanism Interrogation Plate v5.0 (MIPE) Libary2020ACS chemical biology, 07-17, Volume: 15, Issue:7
ISSN: 1554-8937
High-Throughput Screening to Identify Inhibitors of the Type I Interferon-Major Histocompatibility Complex Class I Pathway in Skeletal Muscle.
AID1794808Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL).2014Journal of biomolecular screening, Jul, Volume: 19, Issue:6
ISSN: 1552-454X
A High-Throughput Assay to Identify Inhibitors of the Apicoplast DNA Polymerase from Plasmodium falciparum.
AID1794808Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL).2022Journal of enzyme inhibition and medicinal chemistry, Dec, Volume: 37, Issue:1
ISSN: 1475-6374
AID1345623Human ATM serine/threonine kinase (Other PIKK family kinases)2008Cancer research, Sep-15, Volume: 68, Issue:18
ISSN: 1538-7445
Transient inhibition of ATM kinase is sufficient to enhance cellular sensitivity to ionizing radiation.

Research

Studies (17)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (5.88)29.6817
2010's7 (41.18)24.3611
2020's9 (52.94)2.80

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (5.88%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other16 (94.12%)84.16%
SubstanceStudiesClassesRolesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
rtki cpdaromatic ether;
monochlorobenzenes;
quinazolines
antineoplastic agent;
antiviral agent;
epidermal growth factor receptor antagonist;
geroprotector
00low000000
alfuzosinmonocarboxylic acid amide;
quinazolines;
tetrahydrofuranol
alpha-adrenergic antagonist;
antihypertensive agent;
antineoplastic agent
00low000000
bunazosinquinazolines00low000000
cgs 15943aromatic amine;
biaryl;
furans;
organochlorine compound;
primary amino compound;
quinazolines;
triazoloquinazoline
adenosine A1 receptor antagonist;
adenosine A2A receptor antagonist;
antineoplastic agent;
central nervous system stimulant
00low000000
cl 387785bromobenzenes;
quinazolines;
secondary carboxamide;
ynamide
antineoplastic agent;
EC 2.7.10.1 (receptor protein-tyrosine kinase) inhibitor;
epidermal growth factor receptor antagonist
00low000000
doxazosinaromatic amine;
benzodioxine;
monocarboxylic acid amide;
N-acylpiperazine;
N-arylpiperazine;
quinazolines
alpha-adrenergic antagonist;
antihyperplasia drug;
antihypertensive agent;
antineoplastic agent;
vasodilator agent
00low000000
whi p97quinazolines00low000000
ketanserinaromatic ketone;
organofluorine compound;
piperidines;
quinazolines
alpha-adrenergic antagonist;
antihypertensive agent;
cardiovascular drug;
EC 3.4.21.26 (prolyl oligopeptidase) inhibitor;
serotonergic antagonist
00low000000
metolazoneorganochlorine compound;
quinazolines;
sulfonamide
antihypertensive agent;
diuretic;
ion transport inhibitor
00low000000
pd 153035aromatic amine;
aromatic ether;
bromobenzenes;
quinazolines;
secondary amino compound
EC 2.7.10.1 (receptor protein-tyrosine kinase) inhibitor;
epidermal growth factor receptor antagonist
00low000000
pd168393acrylamides;
bromobenzenes;
quinazolines;
secondary carboxamide;
substituted aniline
epidermal growth factor receptor antagonist00low000000
prazosinaromatic ether;
furans;
monocarboxylic acid amide;
piperazines;
quinazolines
alpha-adrenergic antagonist;
antihypertensive agent;
EC 3.4.21.26 (prolyl oligopeptidase) inhibitor
00low000000
terazosinfurans;
piperazines;
primary amino compound;
quinazolines
alpha-adrenergic antagonist;
antihypertensive agent;
antineoplastic agent
00low000000
methaqualonequinazolinesGABA agonist;
sedative
00low000000
quinethazonequinazolinesantihypertensive agent;
diuretic
00low000000
quinazolinesazaarene;
mancude organic heterobicyclic parent;
ortho-fused heteroarene;
quinazolines
00low000000
mecloqualonequinazolines00low000000
quineloranequinazolines00low000000
halofuginonequinazolines00low000000
glycosinequinazolines00low000000
febrifuginequinazolines00low000000
2,3-trimethylene-4-quinazolonequinazolines00low000000
fenquizonequinazolines00low000000
fenazaquinquinazolinesacaricide;
mitochondrial NADH:ubiquinone reductase inhibitor
00low000000
fluquinconazoleconazole fungicide;
dichlorobenzene;
organofluorine compound;
quinazolines;
triazole fungicide;
triazoles
antifungal agrochemical;
EC 1.14.13.70 (sterol 14alpha-demethylase) inhibitor
00low000000
gefitinibaromatic ether;
monochlorobenzenes;
monofluorobenzenes;
morpholines;
quinazolines;
secondary amino compound;
tertiary amino compound
antineoplastic agent;
epidermal growth factor receptor antagonist
00low000000
cyclazosinaromatic amide;
aromatic ether;
furans;
monocarboxylic acid amide;
quinazolines;
quinoxaline derivative
adenosine A2A receptor antagonist00low000000
glyantrypinequinazolines00low000000
canertinibmonochlorobenzenes;
morpholines;
organofluorine compound;
quinazolines
antineoplastic agent;
tyrosine kinase inhibitor
00low000000
erlotinibaromatic ether;
quinazolines;
secondary amino compound;
terminal acetylenic compound
antineoplastic agent;
epidermal growth factor receptor antagonist;
protein kinase inhibitor
00low000000
lapatinibfurans;
organochlorine compound;
organofluorine compound;
quinazolines
antineoplastic agent;
tyrosine kinase inhibitor
00low000000
(5-amino-3-triazolo[1,5-a]quinazolinyl)-(4-morpholinyl)methanonequinazolines00low000000
mrs 1220quinazolines00low000000
3-deoxyvasicinequinazolines00low000000
N-benzylquinazolin-4-aminebenzenes;
quinazolines;
secondary amino compound
00low000000
2-(4-hydroxy-3-methoxyphenyl)-3-(2-methoxyphenyl)-1,2-dihydroquinazolin-4-onequinazolines00low000000
N-(cyclohexylmethyl)-5,6,7,8-tetrahydrotetrazolo[5,1-b]quinazolin-9-aminequinazolines00low000000
N-(2-pyridinylmethyl)-5,6,7,8-tetrahydro-[1,2,4]triazolo[5,1-b]quinazolin-9-aminequinazolines00low000000
N-[2-methyl-4-oxo-3-(phenylmethyl)-7-(1-piperidinyl)-6-quinazolinyl]-3-pyridinecarboxamidequinazolines00low000000
N-(6-ethoxy-1,3-benzothiazol-2-yl)-2-[[3-(2-furanylmethyl)-4-oxo-2-quinazolinyl]thio]acetamidequinazolines00low000000
2-pyridin-4-yl-2,3-dihydro-1H-quinazolin-4-onequinazolines00low000000
N-[3-(trifluoromethyl)phenyl]-4-quinazolinaminequinazolines00low000000
2-[(2-cyclohexyl-4-quinazolinyl)thio]-N-(4-methyl-1,2,5-oxadiazol-3-yl)acetamidequinazolines00low000000
3-[[[[3-[(4-chlorophenyl)methyl]-2-methyl-4-oxo-6-quinazolinyl]amino]-oxomethyl]amino]propanoic acid ethyl esterquinazolines00low000000
2-[[2-(3,4-dihydro-2H-quinolin-1-yl)-2-oxoethyl]thio]-3-ethyl-4-quinazolinonequinazolines00low000000
2-[(3-ethyl-4-oxo-2-quinazolinyl)thio]acetic acid cyclohexyl esterquinazolines00low000000
2-thiophen-2-yl-2,3-dihydro-1H-quinazolin-4-onequinazolines00low000000
2-(pyridin-4-yl)-4-(pyrrolidin-1-yl)quinazolinepyridines;
pyrrolidines;
quinazolines
00low000000
5-methyl-6-pyridin-4-yl-6H-benzimidazolo[1,2-c]quinazolinequinazolines00low000000
2-[[2-[(2-methoxy-2-oxoethyl)thio]-4-oxo-3-quinazolinyl]oxy]acetic acid methyl esterquinazolines00low000000
2-(1,3-benzoxazol-2-ylamino)-5-spiro[1,6,7,8-tetrahydroquinazoline-4,1'-cyclopentane]onequinazolines00low000000
3-methoxy-2-(3-pyridinylmethylthio)-4-quinazolinonequinazolines00low000000
3,5,5-trimethyl-2-sulfanylidene-1,6-dihydrobenzo[h]quinazolin-4-onequinazolines00low000000
N1-(6-bromo-4-quinazolinyl)-N4,N4-dimethylbenzene-1,4-diaminequinazolines00low000000
N-(3-fluorophenyl)-2-(pyridin-4-yl)quinazolin-4-aminearomatic amine;
monofluorobenzenes;
pyridines;
quinazolines;
secondary amino compound;
substituted aniline
00low000000
3-methyl-2-[2-(4-methyl-5-thiazolyl)ethylthio]-4-quinazolinonequinazolines00low000000
N-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-(4-oxo-3-quinazolinyl)acetamidequinazolines00low000000
6-bromo-3-phenyl-2-sulfanylidene-1H-quinazolin-4-onequinazolines00low000000
N-methyl-2-(4-methylphenyl)-N-(1-methylpiperidin-4-yl)quinazolin-4-aminepiperidines;
quinazolines;
tertiary amino compound;
toluenes
00low000000
2-(2-furanyl)-3-(6-methyl-2-pyridinyl)-4-quinazolinonequinazolines00low000000
2-(4-methoxyphenyl)-3-(3-pyridinyl)-4-quinazolinonequinazolines00low000000
2-phenyl-1H-quinazoline-4-thionequinazolines00low000000
2-(ethylthio)-[1,3,4]thiadiazolo[2,3-b]quinazolin-5-onequinazolines00low000000
2-[(3-methyl-4-oxo-2-quinazolinyl)thio]-N-phenylacetamidequinazolines00low000000
1,3-dimethyl-6-(4-morpholinylsulfonyl)quinazoline-2,4-dionequinazolines00low000000
6,7-dimethoxy-3-phenyl-1H-quinazoline-2,4-dionequinazolines00low000000
6-methoxy-4-methyl-2-[(2-methylphenyl)methylthio]quinazolinequinazolines00low000000
2-(4-chlorophenyl)-4-propan-2-yloxyquinazolinequinazolines00low000000
7-bromo-1,2,3,9-tetrahydropyrrolo[2,1-b]quinazolinequinazolines00low000000
2-(3-methoxyphenyl)-4-propan-2-yloxyquinazolinequinazolines00low000000
2-[[2-(5-methyl-2-thiophenyl)-2-oxoethyl]thio]-3-phenyl-4-quinazolinonequinazolines00low000000
N-(phenylmethyl)-2-[[4-(trifluoromethyl)-5,6-dihydrobenzo[h]quinazolin-2-yl]thio]acetamidequinazolines00low000000
2-(6-amino-2-methyl-4-oxo-3-quinazolinyl)-N-(2-methylphenyl)acetamidequinazolines00low000000
6-amino-3-[(2-chlorophenyl)methyl]-2-propyl-4-quinazolinonequinazolines00low000000
2-(4-chlorophenyl)-N-[2-(4-morpholinyl)ethyl]-4-quinazolinaminequinazolines00low000000
4-(4-ethoxycarbonylanilino)-2-quinazolinecarboxylic acid ethyl esterquinazolines00low000000
4-(4-anilinoanilino)-2-quinazolinecarboxylic acid ethyl esterquinazolines00low000000
2-[[2-(3,4-dihydro-1H-isoquinolin-2-yl)-2-oxoethyl]thio]-3-phenyl-4-quinazolinonequinazolines00low000000
N-(2,4-dimethoxyphenyl)-2-(1-pyrrolidinyl)-4-quinazolinaminequinazolines00low000000
3-(4-oxo-3-quinazolinyl)-N-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)propanamidequinazolines00low000000
4-methoxy-N-[2-[(4-nitrophenyl)methylthio]-4-oxo-3-quinazolinyl]benzamidequinazolines00low000000
N-(4-methoxyphenyl)-2-(3-nitrophenyl)-4-quinazolinaminequinazolines00low000000
2-[(2-tert-butyl-4-quinazolinyl)thio]-N-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)acetamidequinazolines00low000000
1-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-[[2-(phenylmethyl)-4-quinazolinyl]thio]ethanonequinazolines00low000000
2-[(2-propyl-4-quinazolinyl)thio]-N-(4,5,6,7-tetrahydro-1,3-benzothiazol-2-yl)acetamidequinazolines00low000000
1-(3,4-dihydro-1H-isoquinolin-2-yl)-2-[(2-propyl-4-quinazolinyl)thio]ethanonequinazolines00low000000
N-(5-methyl-3-isoxazolyl)-2-[(2-propan-2-yl-4-quinazolinyl)thio]acetamidequinazolines00low000000
Src Inhibitor-1aromatic ether;
polyether;
quinazolines;
secondary amino compound
EC 2.7.10.2 (non-specific protein-tyrosine kinase) inhibitor00low000000
6,7-dimethoxy-N-[(4-methylphenyl)methyl]-4-quinazolinaminequinazolines00low000000
9-methyl-5,6,7,8-tetrahydrotetrazolo[5,1-b]quinazolinequinazolines00low000000
2-[(2,4-dichlorophenyl)methylthio]-6,7-dimethoxy-3-(thiophen-2-ylmethyl)-4-quinazoliniminequinazolines00low000000
7-chloro-N-(2-furanylmethyl)-4-quinazolinaminequinazolines00low000000
4-methoxy-N-(8-methyl-[1,3]dioxolo[4,5-g]quinazolin-6-yl)benzamidequinazolines00low000000
SMER 28organobromine compound;
quinazolines;
secondary amino compound
autophagy inducer00low000000
4-methoxy-2-(4-propoxyphenyl)quinazolinequinazolines00low000000
2-butoxy-3-phenyl-4-quinazolinonequinazolines00low000000
N,N-dibutyl-2-(pyridin-4-yl)quinazolin-4-aminepyridines;
quinazolines;
tertiary amino compound
00low000000
4-chloro-N-(8-methyl-[1,3]dioxolo[4,5-g]quinazolin-6-yl)benzamidequinazolines00low000000
2-(2-bromophenyl)-5-[(7-nitro-4-quinazolinyl)oxymethyl]-1,3,4-oxadiazolequinazolines00low000000
3-[[4-(2-benzofuranyl)-2-thiazolyl]methyl]-2-[(dimethylamino)methyl]-4-quinazolinonequinazolines00low000000
3-(benzenesulfonyl)-N-(3-methylphenyl)-5-triazolo[1,5-a]quinazolinaminequinazolines00low000000
4-[2-[[3-(4-methylphenyl)-5-triazolo[1,5-a]quinazolinyl]amino]ethyl]benzenesulfonamidequinazolines00low000000
6-bromo-3-[4-nitro-3-(trifluoromethyl)phenyl]-2-propyl-4-quinazolinonequinazolines00low000000
12-oxo-N-(4-phenyl-2-thiazolyl)-7,8,9,10-tetrahydro-6H-azepino[2,1-b]quinazoline-3-carboxamidequinazolines00low000000
4,5-dimethyl-2-[[1-oxo-2-(4-quinazolinyloxy)ethyl]amino]-3-thiophenecarboxylic acid ethyl esterquinazolines00low000000
7-[(6,8-dichloro-4-quinazolinyl)oxymethyl]-5-thiazolo[3,2-a]pyrimidinonequinazolines00low000000
N-(2,3-dihydro-1H-inden-5-yl)-2-[[3-(2-fluorophenyl)-4-oxo-2-quinazolinyl]thio]acetamidequinazolines00low000000
2-[[3-(2,4-difluorophenyl)-4-oxo-2-quinazolinyl]thio]-N-(2,3-dihydro-1H-inden-5-yl)acetamidequinazolines00low000000
2-[[3-[(4-fluorophenyl)methyl]-4-oxo-2-quinazolinyl]thio]-N-(thiophen-2-ylmethyl)acetamidequinazolines00low000000
3-(2-furanylmethyl)-4-oxo-N,N-dipropyl-2-sulfanylidene-1H-quinazoline-7-carboxamidequinazolines00low000000
7-(4-quinazolinyloxymethyl)-5-thiazolo[3,2-a]pyrimidinonequinazolines00low000000
N'-(4-quinazolinyl)acetohydrazidequinazolines00low000000
4-methyl-N'-(4-quinazolinyl)benzohydrazidequinazolines00low000000
N-{3-[(2-phenylquinazolin-4-yl)amino]phenyl}acetamideacetamide;
aromatic amine;
quinazolines;
secondary amino compound;
substituted aniline
00low000000
N-(2,3-dihydro-1H-inden-5-yl)-2-[(4-oxo-3-phenyl-2-quinazolinyl)thio]acetamidequinazolines00low000000
2-[(3-butyl-4-oxo-2-quinazolinyl)thio]-N-cyclopropylacetamidequinazolines00low000000
N4-(5-Fluoro-4-imino-3,4-dihydroquinazolin-3-yl)isonicotinamidequinazolines00low000000
3-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-sulfanylidene-1H-quinazolin-4-onequinazolines00low000000
2-[(4-chlorophenyl)methyl]-4-(prop-2-enylthio)quinazolinequinazolines00low000000
2-(4-nitrophenyl)-N-(2-oxolanylmethyl)-4-quinazolinaminequinazolines00low000000
7-chloro-2-methyl-3-(4-pyridylmethyl)-3,4-dihydroquinazolin-4-onequinazolines00low000000
2-[(7-chloro-4-quinazolinyl)oxy]-1-(2,3-dihydro-1,4-benzodioxin-6-yl)ethanonequinazolines00low000000
3,3-dimethyl-1-[[9-(methylthio)-5,6-dihydrothieno[3,4-h]quinazolin-2-yl]thio]-2-butanonequinazolines00low000000
2-(4,6,7-Trimethyl-2-quinazolinyl)guanidinequinazolines00low000000
LSM-19241quinazolines00low000000
LSM-19663quinazolines00low000000
N-[7-(2-furanyl)-5-oxo-7,8-dihydro-6H-quinazolin-2-yl]acetamidequinazolines00low000000
2-(2,4-dichlorophenyl)-3-(phenylmethyl)-1,2-dihydroquinazolin-4-onequinazolines00low000000
4-(3-methoxyphenyl)-3,4,5,6-tetrahydro-1H-benzo[h]quinazoline-2-thionequinazolines00low000000
4-[[3-[2-(1-cyclohexenyl)ethyl]-4-oxo-2-sulfanylidene-1H-quinazolin-7-yl]-oxomethyl]-1-piperazinecarboxylic acid ethyl esterquinazolines00low000000
2-(3-nitrophenyl)-N-(phenylmethyl)-4-quinazolinaminequinazolines00low000000
3-(2-furanylmethyl)-2-phenyl-1,2-dihydroquinazolin-4-onequinazolines00low000000
LSM-19894quinazolines00low000000
importazolequinazolines00low000000
2-(1,3-benzothiazol-2-ylamino)-5-spiro[1,6,7,8-tetrahydroquinazoline-4,1'-cyclopentane]onequinazolines00low000000
6,7-dimethoxy-3-(2-oxolanylmethyl)-2-sulfanylidene-1H-quinazolin-4-onequinazolines00low000000
4-(6-quinolinyl)-1,3,4,6,7,8-hexahydroquinazoline-2,5-dionequinazolines00low000000
9-phenyl-1,5,6,7,8,9-hexahydro-[1,2,4]triazolo[5,1-b]quinazolinequinazolines00low000000
2-[(3-butan-2-yl-4-oxo-2-quinazolinyl)thio]propanenitrilequinazolines00low000000
altanserinquinazolines00low000000
tandutinibaromatic ether;
N-arylpiperazine;
N-carbamoylpiperazine;
phenylureas;
piperidines;
quinazolines;
tertiary amino compound
antineoplastic agent;
EC 2.7.10.1 (receptor protein-tyrosine kinase) inhibitor
00low000000
zd 6474aromatic ether;
organobromine compound;
organofluorine compound;
piperidines;
quinazolines;
secondary amine
antineoplastic agent;
tyrosine kinase inhibitor
00low000000
N-[3,5-dimethyl-1-[(4-methylphenyl)methyl]-4-pyrazolyl]-2-[[4-(trifluoromethyl)-5,6-dihydrobenzo[h]quinazolin-2-yl]thio]acetamidequinazolines00low000000
2-(methylthio)-6-phenyl-6,7-dihydro-5H-[1,2,4]triazolo[5,1-b]quinazolin-8-onequinazolines00low000000
N'-[2-[(2-cyclohexyl-4-quinazolinyl)thio]-1-oxoethyl]-2-methylpropanehydrazidequinazolines00low000000
1-(3,5-dimethyl-1-piperidinyl)-2-[[2-(thiophen-2-ylmethyl)-4-quinazolinyl]thio]ethanonequinazolines00low000000
ml106quinazolines00low000000
6-(1,3-benzodioxol-5-yl)-N-(2-furanylmethyl)-N-methyl-4-quinazolinaminequinazolines00low000000
N-(2-furanylmethyl)-6-(3-methoxyphenyl)-N-methyl-4-quinazolinaminequinazolines00low000000
6-(1,3-benzodioxol-5-yl)-N-[(3-methylphenyl)methyl]-4-quinazolinaminequinazolines00low000000
6-(2-chlorophenyl)-N-(3-pyridinylmethyl)-4-quinazolinaminequinazolines00low000000
6-(3-furanyl)-N-[(3-methylphenyl)methyl]-4-quinazolinaminequinazolines00low000000
6-(3-pyridinyl)-N-(3-pyridinylmethyl)-4-quinazolinaminequinazolines00low000000
6-(3-furanyl)-N-(thiophen-2-ylmethyl)-4-quinazolinaminequinazolines00low000000
6-(3-methoxyphenyl)-N-(3-pyridinylmethyl)-4-quinazolinaminequinazolines00low000000
6-(2-chlorophenyl)-N-(2-furanylmethyl)-N-methyl-4-quinazolinaminequinazolines00low000000
6-(3-methoxyphenyl)-N-(thiophen-2-ylmethyl)-4-quinazolinaminequinazolines00low000000
6-(3-furanyl)-N-(3-pyridinylmethyl)-4-quinazolinaminequinazolines00low000000
N-[(3-methylphenyl)methyl]-6-(3-pyridinyl)-4-quinazolinaminequinazolines00low000000
2-[5-[[2-(3-methoxypropylamino)-2-oxoethyl]thio]-3-oxo-2H-imidazo[1,2-c]quinazolin-2-yl]-N-(phenylmethyl)acetamidequinazolines00low000000
3-[6-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)-6-oxohexyl]-2-sulfanylidene-1H-quinazolin-4-onequinazolines00low000000
3-[2-[butyl(methyl)amino]ethyl]-6-(4-morpholinyl)-2-sulfanylidene-1H-quinazolin-4-onequinazolines00low000000
N-(3-chlorophenyl)-2-[6,7-dimethoxy-2,4-dioxo-3-(2-oxolanylmethyl)-1-quinazolinyl]acetamidequinazolines00low000000
2,4-dioxo-3-pentyl-N-[3-(1-piperidinyl)propyl]-1H-quinazoline-7-carboxamidequinazolines00low000000
2-[(3-oxo-2-propan-2-yl-2H-imidazo[1,2-c]quinazolin-5-yl)thio]-N-[2-(4-sulfamoylphenyl)ethyl]acetamidequinazolines00low000000
2-(6-benzimidazolo[1,2-c]quinazolinylthio)-N-(2-furanylmethyl)acetamidequinazolines00low000000
2-(3-methylanilino)-[1,3,4]thiadiazolo[2,3-b]quinazolin-5-onequinazolines00low000000
3-[4-(1,4-dioxa-8-azaspiro[4.5]decan-8-yl)-4-oxobutyl]-6,7-diethoxy-2-sulfanylidene-1H-quinazolin-4-onequinazolines00low000000
5a,6,7,8,9,10-hexahydro-5H-azepino[2,1-b]quinazolin-12-onequinazolines00low000000
N-(1,3-benzodioxol-5-ylmethyl)-3-cyclopentyl-2,4-dioxo-1H-quinazoline-7-carboxamidequinazolines00low000000
6,7-diethoxy-3-[3-(2-oxo-1-pyrrolidinyl)propyl]-2-sulfanylidene-1H-quinazolin-4-onequinazolines00low000000
2-(1,3-benzodioxol-5-yl)-3-hydroxy-1,2-dihydroquinazolin-4-onequinazolines00low000000
5-(6,7-diethoxy-4-oxo-2-sulfanylidene-1H-quinazolin-3-yl)-N-(2-furanylmethyl)pentanamidequinazolines00low000000
6-chloro-3-[2-(diethylamino)ethyl]-2-sulfanylidene-1H-quinazolin-4-onequinazolines00low000000
2,4-dioxo-3-(2-oxolanylmethyl)-N-pentyl-1H-quinazoline-7-carboxamidequinazolines00low000000
4-[1,3-dioxo-3-[(12-oxo-7,8,9,10-tetrahydro-6H-azepino[2,1-b]quinazolin-2-yl)amino]propyl]-1-piperazinecarboxylic acid ethyl esterquinazolines00low000000
N-butyl-2-[[6-(4-morpholinyl)-4-oxo-3-(2-phenylethyl)-2-quinazolinyl]thio]acetamidequinazolines00low000000
6,7-diethoxy-3-(3-methoxypropyl)-2-sulfanylidene-1H-quinazolin-4-onequinazolines00low000000
savirinquinazolines00low000000
4-[(6,7-diethoxy-2,4-dioxo-1H-quinazolin-3-yl)methyl]-N-(3-methoxypropyl)-1-cyclohexanecarboxamidequinazolines00low000000
6,7-dimethoxy-4-(2-oxolanylmethylamino)-1H-quinazoline-2-thionequinazolines00low000000
N-(5-methyl-1H-pyrazol-3-yl)-2-[[3-oxo-2-(phenylmethyl)-2H-imidazo[1,2-c]quinazolin-5-yl]thio]acetamidequinazolines00low000000
3-(4-chlorophenyl)-2-(1-pyrrolidinyl)-4-quinazolinonequinazolines00low000000
2-[2,4-dioxo-3-(phenylmethyl)-1-quinazolinyl]-N-(5-methyl-3-isoxazolyl)acetamidequinazolines00low000000
2-(2-methylanilino)-[1,3,4]thiadiazolo[2,3-b]quinazolin-5-onequinazolines00low000000
4-[4-oxo-2-[[2-oxo-2-[(phenylmethyl)amino]ethyl]thio]-3-quinazolinyl]-1-piperidinecarboxylic acid ethyl esterquinazolines00low000000
3-hydroxy-2-(2-hydroxy-3-methoxyphenyl)-1,2-dihydroquinazolin-4-onequinazolines00low000000
1-(12-oxo-7,8,9,10-tetrahydro-6H-azepino[2,1-b]quinazolin-2-yl)-3-(3-pyridinylmethyl)thioureaquinazolines00low000000
3-[3-(N-ethylanilino)propyl]-6-(4-morpholinyl)-2-sulfanylidene-1H-quinazolin-4-onequinazolines00low000000
8-methylene-7-(phenylmethyl)-5H-[1,3]dioxolo[4,5-g]quinazoline-6-thionequinazolines00low000000
2-[4-methoxy-3-(4-morpholinylmethyl)phenyl]-3-(phenylmethyl)-1,2-dihydroquinazolin-4-onequinazolines00low000000
N-(4-oxo-2-phenyl-1,2-dihydroquinazolin-3-yl)benzenesulfonamidequinazolines00low000000
N-[2-[(3-nitrophenyl)methylthio]-4-oxo-3-quinazolinyl]benzamidequinazolines00low000000
7-chloro-3-hydroxy-2-[3-(trifluoromethyl)phenyl]-4-quinazolinonequinazolines00low000000
3,5-diethyl-2-(3-hydroxypropylamino)-5-methyl-6H-benzo[h]quinazolin-4-onequinazolines00low000000
3-(2-methoxyphenyl)-2-methyl-4-oxo-1H-quinazoline-2-carboxylic acid methyl esterquinazolines00low000000
1-butyl-1-methyl-3-(12-oxo-7,8,9,10-tetrahydro-6H-azepino[2,1-b]quinazolin-2-yl)thioureaquinazolines00low000000
N,N-diethyl-2-[[7-[(4-methoxyphenyl)methyl]-8-oxo-[1,3]dioxolo[4,5-g]quinazolin-6-yl]thio]acetamidequinazolines00low000000
6-(4-morpholinyl)-3-(2-phenylethyl)-2-sulfanylidene-1H-quinazolin-4-onequinazolines00low000000
N-(1,3-benzodioxol-5-ylmethyl)-6-[6-(4-morpholinyl)-4-oxo-2-sulfanylidene-1H-quinazolin-3-yl]hexanamidequinazolines00low000000
N-[4-oxo-2-(2-pyridinyl)-1,2-dihydroquinazolin-3-yl]acetamidequinazolines00low000000
N-[3-(1-azepanylsulfonyl)-4-methylphenyl]-2-(4-quinazolinylthio)acetamidequinazolines00low000000
3-(2-fluorophenyl)-4-oxo-2-sulfanylidene-1H-quinazoline-7-carboxylic acid methyl esterquinazolines00low000000
2-(2-bromophenyl)-3-[3-(4-morpholinyl)propyl]-1,2-dihydroquinazolin-4-onequinazolines00low000000
sch 79797quinazolines00low000000
3,5-diethyl-2-(2-hydroxyethylamino)-5-methyl-6H-benzo[h]quinazolin-4-onequinazolines00low000000
2-(2-(5-bromo-1h-indol-3-yl)ethyl)-3-(1-methylethoxyphenyl)-4-(3h)-quinazolinonequinazolines00low000000
N-[2-[4-(dimethylamino)phenyl]-4-oxo-1,2-dihydroquinazolin-3-yl]carbamic acid ethyl esterquinazolines00low000000
2-(4-morpholinyl)-10-pyridazino[6,1-b]quinazolinonequinazolines00low000000
N-(4-ethylphenyl)-2-[[3-[3-(4-methyl-1-piperidinyl)propyl]-4-oxo-2-quinazolinyl]thio]acetamidequinazolines00low000000
N-(3-{[2-(2-fluorophenyl)quinazolin-4-yl]amino}phenyl)acetamideacetamide;
aromatic amine;
monofluorobenzenes;
quinazolines;
secondary amino compound;
substituted aniline
00low000000
1-cyclohexyl-3-(12-oxo-7,8,9,10-tetrahydro-6H-azepino[2,1-b]quinazolin-2-yl)thioureaquinazolines00low000000
N-(2-methoxyethyl)-4-oxo-3-[3-(2-oxo-1-pyrrolidinyl)propyl]-2-sulfanylidene-1H-quinazoline-7-carboxamidequinazolines00low000000
4-(4-propan-2-ylphenyl)-3,4,5,6-tetrahydro-1H-benzo[h]quinazolin-2-onequinazolines00low000000
6-(6-bromo-4-oxo-2-sulfanylidene-1H-quinazolin-3-yl)-N-[2-(4-sulfamoylphenyl)ethyl]hexanamidequinazolines00low000000
N-(3-methoxyphenyl)-2-[(4-oxo-3-propyl-2-quinazolinyl)thio]-2-phenylacetamidequinazolines00low000000
2-thiophen-2-yl-N-(thiophen-2-ylmethyl)-4-quinazolinaminequinazolines00low000000
N-(1-benzylpiperidin-4-yl)-2-(pyridin-3-yl)quinazolin-4-aminearomatic amine;
piperidines;
pyridines;
quinazolines;
secondary amino compound;
tertiary amino compound
00low000000
2-(4-oxo-3-quinazolinyl)-N-[3-(1-piperidinylsulfonyl)phenyl]acetamidequinazolines00low000000
N-[2-(4-methoxyphenyl)-4-oxo-1,2-dihydroquinazolin-3-yl]carbamic acid ethyl esterquinazolines00low000000
7-chloro-3-[2-(1-cyclohexenyl)ethyl]-2-sulfanylidene-1H-quinazolin-4-onequinazolines00low000000
4-[2-[[2-[(5-methyl-1H-pyrazol-3-yl)amino]-2-oxoethyl]thio]-4-oxo-3-quinazolinyl]-N-(phenylmethyl)butanamidequinazolines00low000000
2-[[3-butyl-6-(4-morpholinyl)-4-oxo-2-quinazolinyl]thio]acetamidequinazolines00low000000
4-(3,4-dimethoxyphenyl)-3,4,5,6-tetrahydro-1H-benzo[h]quinazoline-2-thionequinazolines00low000000
2-[3-(1-benzotriazolylmethyl)-4-methoxyphenyl]-3-(4-methoxyphenyl)-1,2-dihydroquinazolin-4-onequinazolines00low000000
N-cycloheptyl-3-(2-methoxyethyl)-2,4-dioxo-1H-quinazoline-7-carboxamidequinazolines00low000000
cb676475quinazolines00low000000
1,5-dioxo-2,4-dihydropyrrolo[1,2-a]quinazoline-3-carboxylic acid ethyl esterquinazolines00low000000
GSK3-XIIIaromatic amine;
pyrazoles;
quinazolines;
secondary amino compound
EC 2.7.11.26 (tau-protein kinase) inhibitor00low000000
2-(1,3-benzoxazol-2-ylamino)-7,7-dimethyl-4-(2-pyridinyl)-1,4,6,8-tetrahydroquinazolin-5-onequinazolines00low000000
N-[2-(2-fluorophenyl)ethyl]-5,6,7,8-tetrahydro-[1,2,4]triazolo[5,1-b]quinazolin-9-aminequinazolines00low000000
N-(1,3-benzodioxol-5-ylmethyl)-6-chloro-4-quinazolinaminequinazolines00low000000
N-[3-(4-morpholinyl)propyl]-2,4-dioxo-3-(2-phenylethyl)-1H-quinazoline-7-carboxamidequinazolines00low000000
3-(2-methoxyethyl)-2,4-dioxo-N-pentyl-1H-quinazoline-7-carboxamidequinazolines00low000000
2-[(1-amino-1-oxopropan-2-yl)thio]-3-butyl-4-oxo-7-quinazolinecarboxylic acid methyl esterquinazolines00low000000
ic 871146-aminopurines;
biaryl;
quinazolines
EC 2.7.1.137 (phosphatidylinositol 3-kinase) inhibitor00low000000
zm 447439aromatic ether;
benzamides;
morpholines;
polyether;
quinazolines;
secondary amino compound;
tertiary amino compound
antineoplastic agent;
apoptosis inducer;
Aurora kinase inhibitor
00low000000
linagliptinaminopiperidine;
quinazolines
EC 3.4.14.5 (dipeptidyl-peptidase IV) inhibitor;
hypoglycemic agent
00low000000
bibw 2992aromatic ether;
enamide;
furans;
monochlorobenzenes;
organofluorine compound;
quinazolines;
secondary carboxamide;
tertiary amino compound
antineoplastic agent;
tyrosine kinase inhibitor
00low000000
sotrastaurinindoles;
maleimides;
N-alkylpiperazine;
N-arylpiperazine;
quinazolines
anticoronaviral agent;
EC 2.7.11.13 (protein kinase C) inhibitor;
immunosuppressive agent
00low000000
saracatinibaromatic ether;
benzodioxoles;
diether;
N-methylpiperazine;
organochlorine compound;
oxanes;
quinazolines;
secondary amino compound
anticoronaviral agent;
antineoplastic agent;
apoptosis inducer;
autophagy inducer;
EC 2.7.10.2 (non-specific protein-tyrosine kinase) inhibitor;
radiosensitizing agent
00low000000
luotonin aquinazolines00low000000
PDGF receptor tyrosine kinase inhibitor IIIaromatic ether;
N-arylpiperazine;
N-carbamoylpiperazine;
phenylureas;
quinazolines;
tertiary amino compound
EC 2.7.10.1 (receptor protein-tyrosine kinase) inhibitor00low000000
erastinaromatic ether;
diether;
monochlorobenzenes;
N-acylpiperazine;
N-alkylpiperazine;
quinazolines;
tertiary carboxamide
antineoplastic agent;
ferroptosis inducer;
voltage-dependent anion channel inhibitor
00low000000
azd 8931aromatic ether;
monochlorobenzenes;
monofluorobenzenes;
piperidines;
quinazolines;
secondary amino compound;
tertiary amino compound
EC 2.7.10.1 (receptor protein-tyrosine kinase) inhibitor;
epidermal growth factor receptor antagonist
00low000000
azd 1152anilide;
monoalkyl phosphate;
monofluorobenzenes;
pyrazoles;
quinazolines;
secondary amino compound;
secondary carboxamide;
tertiary amino compound
antineoplastic agent;
Aurora kinase inhibitor;
prodrug
00low000000
pf 00299804enamide;
monochlorobenzenes;
monofluorobenzenes;
piperidines;
quinazolines;
secondary amino compound;
secondary carboxamide;
tertiary amino compound
antineoplastic agent;
epidermal growth factor receptor antagonist
00low000000
lapatinib ditosylatequinazolines00low000000
idelalisibaromatic amine;
organofluorine compound;
purines;
quinazolines;
secondary amino compound
antineoplastic agent;
apoptosis inducer;
EC 2.7.1.137 (phosphatidylinositol 3-kinase) inhibitor
00low000000
N-(2-methoxyethyl)-2-[[3-[(4-methoxyphenyl)methyl]-6-(4-morpholinyl)-4-oxo-2-quinazolinyl]thio]acetamidequinazolines00low000000
4-[(2-methyl-[1,2,4]triazolo[1,5-c]quinazolin-5-yl)hydrazo]-4-oxo-N-propan-2-ylbutanamidequinazolines00low000000
N-butyl-N-methyl-4-[(2-methyl-[1,2,4]triazolo[1,5-c]quinazolin-5-yl)hydrazo]-4-oxobutanamidequinazolines00low000000
2-[4-[1-[(2-fluorophenyl)methyl]-2,4-dioxo-3-quinazolinyl]phenyl]-N-(2-oxolanylmethyl)acetamidequinazolines00low000000
2-[6,7-dimethoxy-3-(3-methoxyphenyl)-2,4-dioxo-1-quinazolinyl]-N-(5-methyl-1H-pyrazol-3-yl)acetamidequinazolines00low000000
N-butyl-3-[1-[(2,5-dimethylphenyl)methyl]-2,4-dioxo-3-quinazolinyl]propanamidequinazolines00low000000
1-[(4-methylphenyl)methyl]-2,4-dioxo-N-(phenylmethyl)-3-prop-2-enyl-7-quinazolinecarboxamidequinazolines00low000000
3-[(4-methoxyphenyl)methyl]-N-(3-methoxypropyl)-2,4-dioxo-1H-quinazoline-7-carboxamidequinazolines00low000000
2-[1-(4-bromophenoxy)butyl]-8,9-dimethoxy-3H-[1,2,4]triazolo[1,5-c]quinazoline-5-thionequinazolines00low000000
azd 1152-hqpaanilide;
monofluorobenzenes;
primary alcohol;
pyrazoles;
quinazolines;
secondary amino compound;
secondary carboxamide;
tertiary amino compound
antineoplastic agent;
Aurora kinase inhibitor
00low000000
N-[3-(diethylamino)propyl]-4-[(2-methyl-[1,2,4]triazolo[1,5-c]quinazolin-5-yl)hydrazo]-4-oxobutanamidequinazolines00low000000
N-(3-ethynylphenyl)-6,7-dimethoxy-4-quinazolinaminequinazolines00low000000
chaetominineindole alkaloid;
lactam;
organic heterotetracyclic compound;
quinazolines
metabolite00low000000
N-[3-(1-azepanyl)propyl]-3-[(4-methoxyphenyl)methyl]-2,4-dioxo-1H-quinazoline-7-carboxamidequinazolines00low000000
2-[[6-(4-morpholinyl)-4-oxo-3-(2-phenylethyl)-2-quinazolinyl]thio]-N-(2-oxolanylmethyl)acetamidequinazolines00low000000
2-[[2-[2-(1-piperidinyl)ethyl]-[1,2,4]triazolo[1,5-c]quinazolin-5-yl]thio]-N-[2-(4-sulfamoylphenyl)ethyl]acetamidequinazolines00low000000
3-(4-methylphenyl)-5-oxo-N-propyl-8-thiazolo[2,3-b]quinazolinecarboxamidequinazolines00low000000
3-(4-methylphenyl)-5-oxo-8-thiazolo[2,3-b]quinazolinecarboxamidequinazolines00low000000
zm323881aromatic ether;
benzyl ether;
fluorophenol;
halophenol;
monofluorobenzenes;
organic cation;
quinazolines;
secondary amino compound;
substituted aniline
vascular endothelial growth factor receptor antagonist00low000000
6-(3,5-dimethyl-4-isoxazolyl)-N-[(3-methoxyphenyl)methyl]-4-quinazolinaminequinazolines00low000000
6-(3,5-dimethyl-4-isoxazolyl)-N-[(2-ethoxyphenyl)methyl]-4-quinazolinaminequinazolines00low000000
N-[4-[[[6-(3,5-dimethyl-4-isoxazolyl)-4-quinazolinyl]amino]methyl]phenyl]acetamidequinazolines00low000000
6-(3,5-dimethyl-4-isoxazolyl)-N-[(1-methyl-2-piperidinyl)methyl]-4-quinazolinaminequinazolines00low000000
6-(3,5-dimethyl-4-isoxazolyl)-N-[1-(2-furanyl)ethyl]-4-quinazolinaminequinazolines00low000000
6-(3,5-dimethyl-4-isoxazolyl)-N-[(3-methyl-2-thiophenyl)methyl]-4-quinazolinaminequinazolines00low000000
4-[2-[(6-chloro-4-quinazolinyl)amino]ethyl]phenolquinazolines00low000000
ast 1306quinazolines00low000000
2-[[2-(phenoxymethyl)-4-quinazolinyl]thio]acetic acid methyl esterquinazolines00low000000
poziotinibacrylamides;
aromatic ether;
dichlorobenzene;
diether;
monofluorobenzenes;
N-acylpiperidine;
quinazolines;
secondary amino compound;
substituted aniline
antineoplastic agent;
apoptosis inducer;
epidermal growth factor receptor antagonist
00low000000
N-[4-[[5-[5-hydroxy-4-oxo-3-(phenylmethyl)-1,2-dihydroquinazolin-2-yl]-2-methoxyphenyl]methoxy]phenyl]acetamidequinazolines00low000000
N-(2-furanylmethyl)-N-methyl-6-(1-methyl-5-indolyl)-4-quinazolinaminequinazolines00low000000
6-(2-chlorophenyl)-N-[(3-methylphenyl)methyl]-4-quinazolinaminequinazolines00low000000
6-(3-methoxyphenyl)-N-[(3-methylphenyl)methyl]-4-quinazolinaminequinazolines00low000000
6-(2,3-dihydro-1,4-benzodioxin-6-yl)-N-[(3-methylphenyl)methyl]-4-quinazolinaminequinazolines00low000000
6-(2-chlorophenyl)-N-(thiophen-2-ylmethyl)-4-quinazolinaminequinazolines00low000000
6-(3-chlorophenyl)-N-(thiophen-2-ylmethyl)-4-quinazolinaminequinazolines00low000000
6-(3-pyridinyl)-N-(thiophen-2-ylmethyl)-4-quinazolinaminequinazolines00low000000
6-(3-methylphenyl)-N-(thiophen-2-ylmethyl)-4-quinazolinaminequinazolines00low000000
6-(1-methyl-5-indolyl)-N-(thiophen-2-ylmethyl)-4-quinazolinaminequinazolines00low000000
6-(2,3-dihydro-1,4-benzodioxin-6-yl)-N-(thiophen-2-ylmethyl)-4-quinazolinaminequinazolines00low000000
N-(1,3-benzodioxol-5-ylmethyl)-6-(2,3-dihydro-1,4-benzodioxin-6-yl)-4-quinazolinaminequinazolines00low000000
6-(2,3-dihydro-1,4-benzodioxin-6-yl)-N-(3-pyridinylmethyl)-4-quinazolinaminequinazolines00low000000
6-(1,3-benzodioxol-5-yl)-N-[(3-fluorophenyl)methyl]-4-quinazolinaminequinazolines00low000000
6-(3-chlorophenyl)-N-(3-pyridinylmethyl)-4-quinazolinaminequinazolines00low000000
6-(3-methylphenyl)-N-(3-pyridinylmethyl)-4-quinazolinaminequinazolines00low000000
6-(1,3-benzodioxol-5-yl)-N-(3-pyridinylmethyl)-4-quinazolinaminequinazolines00low000000
N-(1,3-benzodioxol-5-ylmethyl)-6-(2-chlorophenyl)-4-quinazolinaminequinazolines00low000000
N-(1,3-benzodioxol-5-ylmethyl)-6-(3-methoxyphenyl)-4-quinazolinaminequinazolines00low000000
N-(1,3-benzodioxol-5-ylmethyl)-6-(3-pyridinyl)-4-quinazolinaminequinazolines00low000000
N-(1,3-benzodioxol-5-ylmethyl)-6-(3-furanyl)-4-quinazolinaminequinazolines00low000000
6-(2-chlorophenyl)-N-[(4-methyl-2-thiophenyl)methyl]-4-quinazolinaminequinazolines00low000000
6-(3-chlorophenyl)-N-[(4-methyl-2-thiophenyl)methyl]-4-quinazolinaminequinazolines00low000000
6-(3-methoxyphenyl)-N-[(4-methyl-2-thiophenyl)methyl]-4-quinazolinaminequinazolines00low000000
N-[(4-methyl-2-thiophenyl)methyl]-6-(3-pyridinyl)-4-quinazolinaminequinazolines00low000000
6-(1,3-benzodioxol-5-yl)-N-[(4-methyl-2-thiophenyl)methyl]-4-quinazolinaminequinazolines00low000000
6-(2,3-dihydro-1,4-benzodioxin-6-yl)-N-[(4-methyl-2-thiophenyl)methyl]-4-quinazolinaminequinazolines00low000000
6-(3-furanyl)-N-[(4-methyl-2-thiophenyl)methyl]-4-quinazolinaminequinazolines00low000000
4-[5-(3-hydroxy-4-oxo-1,2-dihydroquinazolin-2-yl)-2-furanyl]benzonitrilequinazolines00low000000
2-[5-(2-fluorophenyl)-2-furanyl]-3-hydroxy-1,2-dihydroquinazolin-4-onequinazolines00low000000
3-hydroxy-2-(5-thiophen-2-yl-2-furanyl)-1,2-dihydroquinazolin-4-onequinazolines00low000000
2-[5-(3-fluorophenyl)-2-furanyl]-3-hydroxy-1,2-dihydroquinazolin-4-onequinazolines00low000000
3-hydroxy-2-[5-[4-(trifluoromethyl)phenyl]-2-furanyl]-1,2-dihydroquinazolin-4-onequinazolines00low000000
6-(1,3-benzodioxol-5-yl)-N-methyl-N-(thiophen-2-ylmethyl)-4-quinazolinaminequinazolines00low000000
[5-[4-[(5-methyl-2-furanyl)methylamino]-6-quinazolinyl]-2-furanyl]methanolquinazolines00low000000
unc 0638quinazolines00low000000
unc 0321quinazolines00low000000
ML240aromatic amine;
aromatic ether;
benzimidazoles;
primary amino compound;
quinazolines;
secondary amino compound
antineoplastic agent00low000000
ncgc00242364quinazolines00low000000
2-methoxy-N-[3-[4-[3-methyl-4-[(6-methyl-3-pyridinyl)oxy]anilino]-6-quinazolinyl]prop-2-enyl]acetamidearomatic ether;
methylpyridines;
olefinic compound;
quinazolines;
secondary amino compound;
secondary carboxamide;
toluenes
00low000000
N-[4-(3-chloro-4-fluoroanilino)-7-[[(3S)-3-oxolanyl]oxy]-6-quinazolinyl]-4-(dimethylamino)-2-butenamidequinazolines00low000000
N-[4-(3-chloro-4-fluoroanilino)-7-methoxy-6-quinazolinyl]-4-(1-piperidinyl)-2-butenamidequinazolines00low000000
2-methoxy-n-(3-methyl-2-oxo-1,2,3,4-tetrahydroquinazolin-6-yl)benzenesulfonamidequinazolines00low000000
nu 1025phenols;
quinazolines
EC 2.4.2.30 (NAD(+) ADP-ribosyltransferase) inhibitor00low000000
1-[amino-[(6-methoxy-4-methyl-2-quinazolinyl)amino]methylidene]-3-phenylureaquinazolines00low000000
4-oxo-2-(trifluoromethyl)-1H-quinazoline-6-carboxylic acid ethyl esterquinazolines00low000000
4-hydroxyquinazolinequinazolines00low000000
2-(3,4-dihydro-1H-isoquinolin-2-ylmethyl)-1H-quinazolin-4-onequinazolines00low000000
2-[(2-methyl-2,3-dihydroindol-1-yl)methyl]-4-oxo-1H-quinazoline-7-carboxylic acid methyl esterquinazolines00low000000
2-[[[5,7-bis(ethylamino)-[1,2,4]triazolo[4,3-a][1,3,5]triazin-3-yl]thio]methyl]-1H-quinazolin-4-onequinazolines00low000000
3-(4-oxo-1H-quinazolin-2-yl)propanoic acid (3,5-dimethyl-4-isoxazolyl)methyl esterquinazolines00low000000
N-(1,3-benzodioxol-5-ylmethyl)-3-methoxy-N-[(4-oxo-1H-quinazolin-2-yl)methyl]benzamidequinazolines00low000000
1-cyclopentyl-1-[(4-oxo-1H-quinazolin-2-yl)methyl]-3-(phenylmethyl)ureaquinazolines00low000000
6,8-dibromo-2-[[[4-(difluoromethoxy)phenyl]methyl-methylamino]methyl]-1H-quinazolin-4-onequinazolines00low000000
2-(5'-chloro-2'-phosphoryloxyphenyl)-6-chloro-4-(3h)-quinazolinonearyl phosphate;
monochlorobenzenes;
quinazolines
fluorochrome00low000000
glycosmininequinazolines00low000000
N-[(4-oxo-1H-quinazolin-2-yl)methyl]-N-(2-phenylethyl)butanamidequinazolines00low000000
2-(4-methoxyphenyl)-1H-quinazolin-4-onequinazolines00low000000
2-[(7-methoxy-4-methyl-2-quinazolinyl)amino]-5,6-dimethyl-1H-pyrimidin-4-onequinazolines00low000000
6,7-dimethoxy-2-[(1H-1,2,4-triazol-5-ylthio)methyl]-1H-quinazolin-4-onequinazolines00low000000
2-[(dimethylamino)methyl]-4-spiro[1,6-dihydrobenzo[h]quinazoline-5,1'-cyclohexane]onequinazolines00low000000
2-(diethylaminomethyl)-4-spiro[1,6-dihydrobenzo[h]quinazoline-5,1'-cyclohexane]onequinazolines00low000000
2-[5-(3-chlorophenyl)-2-furanyl]-1H-quinazolin-4-onequinazolines00low000000
2-[(6-ethyl-4-methyl-2-quinazolinyl)amino]-1H-quinazolin-4-onequinazolines00low000000
2-[(2-pyridinylthio)methyl]-1H-quinazolin-4-onequinazolines00low000000
5,5-diethyl-2-(2-hydroxyethylamino)-1,6-dihydrobenzo[h]quinazolin-4-onequinazolines00low000000
1-[(7-chloro-4-oxo-1H-quinazolin-2-yl)methyl]-4-piperidinecarboxamidequinazolines00low000000
3-ethyl-2-[(4-oxo-1H-quinazolin-2-yl)methylthio]-4-quinazolinonequinazolines00low000000
6,7-dimethoxy-2-[[methyl-[(4-oxo-1H-quinazolin-2-yl)methyl]amino]methyl]-1H-quinazolin-4-onequinazolines00low000000
2-[(6-ethyl-4-methyl-2-quinazolinyl)amino]-6-(methoxymethyl)-1H-pyrimidin-4-onequinazolines00low000000
5,5-diethyl-2-hydrazinyl-1,6-dihydrobenzo[h]quinazolin-4-onequinazolines00low000000
3-(3-ethoxypropyl)-1-[(4-oxo-1H-quinazolin-2-yl)methyl]-1-(phenylmethyl)thioureaquinazolines00low000000
chrysoginecyclic amide;
quinazoline alkaloid;
quinazolines;
secondary alcohol;
secondary amide
Aspergillus metabolite;
biological pigment;
marine metabolite
00low000000
N-[(cyclohexylamino)-oxomethyl]-2-[ethyl-[(4-oxo-1H-quinazolin-2-yl)methyl]amino]acetamidequinazolines00low000000
7-[[ethyl-[(4-oxo-1H-quinazolin-2-yl)methyl]amino]methyl]-5-thiazolo[3,2-a]pyrimidinonequinazolines00low000000
2-[[(6-ethyl-4-oxo-3-prop-2-enyl-2-thieno[2,3-d]pyrimidinyl)thio]methyl]-4-oxo-1H-quinazoline-7-carboxylic acid methyl esterquinazolines00low000000
ARS-1620quinazolinesantineoplastic agent;
antiviral agent;
inhibitor
00low000000
SubstanceStudiesClassesRolesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
pk 11195aromatic amide;
isoquinolines;
monocarboxylic acid amide;
monochlorobenzenes
antineoplastic agent2013201311.0low000010
pd 173074aromatic amine;
biaryl;
dimethoxybenzene;
pyridopyrimidine;
tertiary amino compound;
ureas
antineoplastic agent;
EC 2.7.10.1 (receptor protein-tyrosine kinase) inhibitor;
fibroblast growth factor receptor antagonist
2013201311.0low000010
abt 702bipyridines2013201311.0low000010
aurintricarboxylic acidmonohydroxybenzoic acid;
quinomethanes;
tricarboxylic acid
fluorochrome;
histological dye;
insulin-like growth factor receptor 1 antagonist
202020204.0low000010
bicalutamide(trifluoromethyl)benzenes;
monocarboxylic acid amide;
monofluorobenzenes;
nitrile;
sulfone;
tertiary alcohol
2013201311.0low000010
verapamilaromatic ether;
nitrile;
polyether;
tertiary amino compound
2013201311.0low000010
celecoxiborganofluorine compound;
pyrazoles;
sulfonamide;
toluenes
cyclooxygenase 2 inhibitor;
geroprotector;
non-narcotic analgesic;
non-steroidal anti-inflammatory drug
2013201311.0low000010
chelerythrinebenzophenanthridine alkaloid;
organic cation
antibacterial agent;
antineoplastic agent;
EC 2.7.11.13 (protein kinase C) inhibitor
2013201311.0low000010
chloroquineaminoquinoline;
organochlorine compound;
secondary amino compound;
tertiary amino compound
anticoronaviral agent;
antimalarial;
antirheumatic drug;
autophagy inhibitor;
dermatologic drug
202220222.0low000001
furosemidechlorobenzoic acid;
furans;
sulfonamide
environmental contaminant;
loop diuretic;
xenobiotic
2013201311.0low000010
gossypol201320207.5low000020
fasudilisoquinolines;
N-sulfonyldiazepane
antihypertensive agent;
calcium channel blocker;
EC 2.7.11.1 (non-specific serine/threonine protein kinase) inhibitor;
geroprotector;
neuroprotective agent;
nootropic agent;
vasodilator agent
2013201311.0low000010
indirubin-3'-monoxime2013201311.0low000010
leflunomide(trifluoromethyl)benzenes;
isoxazoles;
monocarboxylic acid amide
antineoplastic agent;
antiparasitic agent;
EC 1.3.98.1 [dihydroorotate oxidase (fumarate)] inhibitor;
EC 3.1.3.16 (phosphoprotein phosphatase) inhibitor;
hepatotoxic agent;
immunosuppressive agent;
non-steroidal anti-inflammatory drug;
prodrug;
pyrimidine synthesis inhibitor;
tyrosine kinase inhibitor
2013201311.0low000010
letrozolenitrile;
triazoles
antineoplastic agent;
EC 1.14.14.14 (aromatase) inhibitor
2013201311.0low000010
lg 1002682013201311.0low000010
2-(4-morpholinyl)-8-phenyl-4h-1-benzopyran-4-onechromones;
morpholines;
organochlorine compound
autophagy inhibitor;
EC 2.7.1.137 (phosphatidylinositol 3-kinase) inhibitor;
geroprotector
202020204.0low000010
metforminguanidinesenvironmental contaminant;
geroprotector;
hypoglycemic agent;
xenobiotic
2013201311.0low000010
mitoxantronedihydroxyanthraquinoneanalgesic;
antineoplastic agent
2013201311.0low000010
entinostatbenzamides;
carbamate ester;
primary amino compound;
pyridines;
substituted aniline
antineoplastic agent;
apoptosis inducer;
EC 3.5.1.98 (histone deacetylase) inhibitor
2013201311.0low000010
olprinonebipyridines2013201311.0low000010
omeprazolearomatic ether;
benzimidazoles;
pyridines;
sulfoxide
2013201311.0low000010
pioglitazonearomatic ether;
pyridines;
thiazolidinediones
antidepressant;
cardioprotective agent;
EC 2.7.1.33 (pantothenate kinase) inhibitor;
EC 6.2.1.3 (long-chain-fatty-acid--CoA ligase) inhibitor;
ferroptosis inhibitor;
geroprotector;
hypoglycemic agent;
insulin-sensitizing drug;
PPARgamma agonist;
xenobiotic
2013201311.0low000010
3-[(3,5-dibromo-4-hydroxyphenyl)methylidene]-5-iodo-1H-indol-2-oneindoles2013201311.0low000010
riluzolebenzothiazoles2013201311.0low000010
sb 206553pyrroloindole2013201311.0low000010
sb 220025aminopyrimidine;
imidazoles;
organofluorine compound;
piperidines
angiogenesis inhibitor;
anti-inflammatory agent;
EC 2.7.11.24 (mitogen-activated protein kinase) inhibitor
2013201311.0low000010
sb 202190imidazoles;
organofluorine compound;
phenols;
pyridines
apoptosis inducer;
EC 2.7.11.24 (mitogen-activated protein kinase) inhibitor
2013201311.0low000010
sk&f 86002imidazoles2013201311.0low000010
imatinibaromatic amine;
benzamides;
N-methylpiperazine;
pyridines;
pyrimidines
antineoplastic agent;
apoptosis inducer;
tyrosine kinase inhibitor
2013201311.0low000010
vorinostatdicarboxylic acid diamide;
hydroxamic acid
antineoplastic agent;
apoptosis inducer;
EC 3.5.1.98 (histone deacetylase) inhibitor
2013201311.0low000010
sulfasalazine2013201311.0low000010
2-[4-(1,2-diphenylbut-1-enyl)phenoxy]-N,N-dimethylethanaminestilbenoid2013201311.0low000010
troglitazonechromanes;
thiazolidinone
anticoagulant;
anticonvulsant;
antineoplastic agent;
antioxidant;
EC 6.2.1.3 (long-chain-fatty-acid--CoA ligase) inhibitor;
ferroptosis inhibitor;
hypoglycemic agent;
platelet aggregation inhibitor;
vasodilator agent
2013201311.0low000010
azacitidineN-glycosyl-1,3,5-triazine;
nucleoside analogue
antineoplastic agent2013201311.0low000010
podophyllotoxinfuronaphthodioxole;
lignan;
organic heterotetracyclic compound
antimitotic;
antineoplastic agent;
keratolytic drug;
microtubule-destabilising agent;
plant metabolite;
tubulin modulator
2013201311.0low000010
formestane17-oxo steroid;
3-oxo-Delta(4) steroid;
enol;
hydroxy steroid
antineoplastic agent;
EC 1.14.14.14 (aromatase) inhibitor
2013201311.0low000010
hydroxychloroquine sulfate2013201311.0low000010
amiloride hydrochloride, anhydroushydrochloridediuretic;
sodium channel blocker
2013201311.0low000010
acadesine1-ribosylimidazolecarboxamide;
aminoimidazole;
nucleoside analogue
antineoplastic agent;
platelet aggregation inhibitor
2013201311.0low000010
cladribineorganochlorine compound;
purine 2'-deoxyribonucleoside
antineoplastic agent;
immunosuppressive agent
2013201311.0low000010
zidovudineazide;
pyrimidine 2',3'-dideoxyribonucleoside
antimetabolite;
antiviral drug;
HIV-1 reverse transcriptase inhibitor
2013201311.0low000010
etoposidebeta-D-glucoside;
furonaphthodioxole;
organic heterotetracyclic compound
antineoplastic agent;
DNA synthesis inhibitor
202220222.0low000001
lonidaminedichlorobenzene;
indazoles;
monocarboxylic acid
antineoplastic agent;
antispermatogenic agent;
EC 2.7.1.1 (hexokinase) inhibitor;
geroprotector
2013201311.0low000010
simvastatindelta-lactone;
fatty acid ester;
hexahydronaphthalenes;
statin (semi-synthetic)
EC 1.1.1.34/EC 1.1.1.88 (hydroxymethylglutaryl-CoA reductase) inhibitor;
EC 3.4.24.83 (anthrax lethal factor endopeptidase) inhibitor;
ferroptosis inducer;
geroprotector;
prodrug
2013201311.0low000010
itraconazolearomatic ether;
conazole antifungal drug;
cyclic ketal;
dichlorobenzene;
dioxolane;
N-arylpiperazine;
triazole antifungal drug;
triazoles
EC 3.6.3.44 (xenobiotic-transporting ATPase) inhibitor;
Hedgehog signaling pathway inhibitor;
P450 inhibitor
2013201311.0low000010
pravadoline2013201311.0low000010
zileuton1-benzothiophenes;
ureas
anti-asthmatic drug;
EC 1.13.11.34 (arachidonate 5-lipoxygenase) inhibitor;
ferroptosis inhibitor;
leukotriene antagonist;
non-steroidal anti-inflammatory drug
2013201311.0low000010
niguldipinediarylmethane2013201311.0low000010
topotecanpyranoindolizinoquinolineantineoplastic agent;
EC 5.99.1.2 (DNA topoisomerase) inhibitor
2013201311.0low000010
eliprodilmonochlorobenzenes;
monofluorobenzenes;
piperidines;
secondary alcohol;
tertiary amino compound
2013201311.0low000010
gemcitabineorganofluorine compound;
pyrimidine 2'-deoxyribonucleoside
antimetabolite;
antineoplastic agent;
antiviral drug;
DNA synthesis inhibitor;
EC 1.17.4.1 (ribonucleoside-diphosphate reductase) inhibitor;
environmental contaminant;
immunosuppressive agent;
photosensitizing agent;
prodrug;
radiosensitizing agent;
xenobiotic
2013201311.0low000010
irinotecancarbamate ester;
delta-lactone;
N-acylpiperidine;
pyranoindolizinoquinoline;
ring assembly;
tertiary alcohol;
tertiary amino compound
antineoplastic agent;
apoptosis inducer;
EC 5.99.1.2 (DNA topoisomerase) inhibitor;
prodrug
201620225.0low000011
verapamil hydrochloride2013201311.0low000010
efavirenzacetylenic compound;
benzoxazine;
cyclopropanes;
organochlorine compound;
organofluorine compound
antiviral drug;
HIV-1 reverse transcriptase inhibitor
2013201311.0low000010
epigallocatechin gallateflavans;
gallate ester;
polyphenol
antineoplastic agent;
antioxidant;
apoptosis inducer;
geroprotector;
Hsp90 inhibitor;
neuroprotective agent;
plant metabolite
202020204.0low000010
bendamustinebenzimidazoles2013201311.0low000010
caroverinequinoxaline derivative2013201311.0low000010
cgs 9343bbenzimidazoles2013201311.0low000010
telmisartanbenzimidazoles;
biphenyls;
carboxybiphenyl
angiotensin receptor antagonist;
antihypertensive agent;
EC 3.4.15.1 (peptidyl-dipeptidase A) inhibitor;
environmental contaminant;
xenobiotic
2013201311.0low000010
2-methoxyestradiol17beta-hydroxy steroid;
3-hydroxy steroid
angiogenesis modulating agent;
antimitotic;
antineoplastic agent;
human metabolite;
metabolite;
mouse metabolite
2013201311.0low000010
alaceprildipeptide;
thioacetate ester
EC 3.4.15.1 (peptidyl-dipeptidase A) inhibitor2013201311.0low000010
ubenimex2013201311.0low000010
gallocatecholcatechin;
flavan-3,3',4',5,5',7-hexol
antioxidant;
food component;
plant metabolite
202020204.0low000010
strictinin202020204.0low000010
vinpocetine2013201311.0medium000010
6-hydroxydopanon-proteinogenic alpha-amino acid202020204.0low000010
deguelinaromatic ether;
diether;
organic heteropentacyclic compound;
rotenones
angiogenesis inhibitor;
anti-inflammatory agent;
antineoplastic agent;
antiviral agent;
apoptosis inducer;
EC 2.7.11.1 (non-specific serine/threonine protein kinase) inhibitor;
mitochondrial NADH:ubiquinone reductase inhibitor;
plant metabolite
2013201311.0low000010
triptolidediterpenoid;
epoxide;
gamma-lactam;
organic heteroheptacyclic compound
antispermatogenic agent;
plant metabolite
2013201311.0low000010
sr 48692N-acyl-amino acid2013201311.0low000010
elacridar2013201311.0low000010
gefitinibaromatic ether;
monochlorobenzenes;
monofluorobenzenes;
morpholines;
quinazolines;
secondary amino compound;
tertiary amino compound
antineoplastic agent;
epidermal growth factor receptor antagonist
2013201311.0low000010
bay x 10052013201311.0low000010
gyki 536552013201311.0low000010
ml-30002013201311.0low000010
cd 437adamantanes;
monocarboxylic acid;
naphthoic acid;
phenols
apoptosis inducer;
retinoic acid receptor gamma agonist
2013201311.0low000010
docetaxel anhydroussecondary alpha-hydroxy ketone;
tetracyclic diterpenoid
antimalarial;
antineoplastic agent;
photosensitizing agent
2013201311.0low000010
perifosineammonium betaine;
phospholipid
EC 2.7.1.137 (phosphatidylinositol 3-kinase) inhibitor2013201311.0low000010
mk 7672013201311.0low000010
bazedoxifene acetate2013201311.0medium000010
canertinibmonochlorobenzenes;
morpholines;
organofluorine compound;
quinazolines
antineoplastic agent;
tyrosine kinase inhibitor
2013201311.0low000010
birb 796aromatic ether;
morpholines;
naphthalenes;
pyrazoles;
ureas
EC 2.7.11.24 (mitogen-activated protein kinase) inhibitor;
immunomodulator
2013201311.0low000010
tipifarnibimidazoles;
monochlorobenzenes;
primary amino compound;
quinolone
antineoplastic agent;
apoptosis inducer;
EC 2.5.1.58 (protein farnesyltransferase) inhibitor
2013201311.0low000010
cyc 2022,6-diaminopurinesantiviral drug;
EC 2.7.11.22 (cyclin-dependent kinase) inhibitor
2013201311.0low000010
sb 203580imidazoles;
monofluorobenzenes;
pyridines;
sulfoxide
EC 2.7.11.1 (non-specific serine/threonine protein kinase) inhibitor;
EC 2.7.11.24 (mitogen-activated protein kinase) inhibitor;
geroprotector;
Hsp90 inhibitor;
neuroprotective agent
2013201311.0low000010
enzastaurinindoles;
maleimides
2013201311.0low000010
erlotinibaromatic ether;
quinazolines;
secondary amino compound;
terminal acetylenic compound
antineoplastic agent;
epidermal growth factor receptor antagonist;
protein kinase inhibitor
2013201311.0low000010
piboserod2013201311.0low000010
l 1631912013201311.0low000010
bd 1047primary amine2013201311.0low000010
lapatinibfurans;
organochlorine compound;
organofluorine compound;
quinazolines
antineoplastic agent;
tyrosine kinase inhibitor
2013201311.0low000010
sorafenib(trifluoromethyl)benzenes;
aromatic ether;
monochlorobenzenes;
phenylureas;
pyridinecarboxamide
angiogenesis inhibitor;
anticoronaviral agent;
antineoplastic agent;
EC 2.7.11.1 (non-specific serine/threonine protein kinase) inhibitor;
ferroptosis inducer;
tyrosine kinase inhibitor
2013201311.0low000010
lenalidomidearomatic amine;
dicarboximide;
isoindoles;
piperidones
angiogenesis inhibitor;
antineoplastic agent;
immunomodulator
2013201311.0low000010
N-[4-(3-chloro-4-fluoroanilino)-3-cyano-7-ethoxy-6-quinolinyl]-4-(dimethylamino)-2-butenamideaminoquinoline2013201311.0medium000010
sr 1428062013201311.0low000010
elesclomolcarbohydrazide;
thiocarbonyl compound
antineoplastic agent;
apoptosis inducer
2013201311.0low000010
nsc 663284quinolone2013201311.0low000010
bortezomibamino acid amide;
L-phenylalanine derivative;
pyrazines
antineoplastic agent;
antiprotozoal drug;
protease inhibitor;
proteasome inhibitor
2013201311.0low000010
bardoxolone methylcyclohexenones2013201311.0low000010
nsc 23766aminopyrimidine;
aminoquinoline;
primary amino compound;
secondary amino compound;
tertiary amino compound
antiviral agent;
apoptosis inducer;
EC 3.6.5.2 (small monomeric GTPase) inhibitor;
muscarinic antagonist
2013201311.0low000010
gw 3965diarylmethane2013201311.0low000010
y 27632aromatic amide2013201311.0low000010
6-bromoindirubin-3'-oxime2013201311.0low000010
purvalanol bpurvalanolprotein kinase inhibitor2013201311.0low000010
y-7002013201311.0low000010
repsoxpyrazolopyridine2013201311.0low000010
4,4-difluoro-N-[(1S)-3-[3-(3-methyl-5-propan-2-yl-1,2,4-triazol-4-yl)-8-azabicyclo[3.2.1]octan-8-yl]-1-phenylpropyl]-1-cyclohexanecarboxamidetropane alkaloid2013201311.0medium000010
s 1033(trifluoromethyl)benzenes;
imidazoles;
pyridines;
pyrimidines;
secondary amino compound;
secondary carboxamide
anticoronaviral agent;
antineoplastic agent;
tyrosine kinase inhibitor
2013201311.0low000010
mercaptopurinearyl thiol;
purines;
thiocarbonyl compound
anticoronaviral agent;
antimetabolite;
antineoplastic agent
2013201311.0low000010
rg108indolyl carboxylic acid2013201311.0low000010
stf 0830102013201311.0medium000010
N-(3-cyano-4,5,6,7-tetrahydro-1-benzothiophen-2-yl)-1-naphthalenecarboxamidenaphthalenecarboxamide2013201311.0low000010
cct018159benzodioxine;
pyrazoles;
resorcinols
antineoplastic agent;
apoptosis inducer;
Hsp90 inhibitor
2013201311.0low000010
secinh3triazoles2013201311.0low000010
jk1842013201311.0low000010
tamoxifen citratecitrate saltangiogenesis inhibitor;
anticoronaviral agent
2013201311.0low000010
hc-0670472013201311.0low000010
bi-78d3aryl sulfide2013201311.0low000010
gsk 37872013201311.0low000010
methyl-thiohydantoin-tryptophanorganonitrogen compound;
organooxygen compound
2013201311.0low000010
2-[2-chloro-6-ethoxy-4-[(3-methyl-5-oxo-1-phenyl-4-pyrazolylidene)methyl]phenoxy]acetic acid methyl estermonocarboxylic acid2013201311.0medium000010
4-(5-(4-methoxyphenyl)-3-phenyl-4,5-dihydro-1h-pyrazol-1-yl)benzenesulfonamidesulfonamide2013201311.0low000010
LSM-1318oxa-steroid2013201311.0low000010
rwj 676572013201311.0low000010
6-methyl-2-(phenylethynyl)pyridineacetylenic compound;
methylpyridines
anxiolytic drug;
metabotropic glutamate receptor antagonist
2013201311.0low000010
bms 3870321,3-oxazoles;
1,3-thiazoles;
organic sulfide;
piperidinecarboxamide;
secondary carboxamide
angiogenesis inhibitor;
antineoplastic agent;
apoptosis inducer;
EC 2.7.11.22 (cyclin-dependent kinase) inhibitor
2013201311.0low000010
tandutinibaromatic ether;
N-arylpiperazine;
N-carbamoylpiperazine;
phenylureas;
piperidines;
quinazolines;
tertiary amino compound
antineoplastic agent;
EC 2.7.10.1 (receptor protein-tyrosine kinase) inhibitor
2013201311.0low000010
vx-745aryl sulfide;
dichlorobenzene;
difluorobenzene;
pyrimidopyridazine
anti-inflammatory drug;
apoptosis inducer;
EC 2.7.11.24 (mitogen-activated protein kinase) inhibitor
2013201311.0low000010
corlanorhydrochloridecardiotonic drug2013201311.0medium000010
dasatinib1,3-thiazoles;
aminopyrimidine;
monocarboxylic acid amide;
N-(2-hydroxyethyl)piperazine;
N-arylpiperazine;
organochlorine compound;
secondary amino compound;
tertiary amino compound
anticoronaviral agent;
antineoplastic agent;
tyrosine kinase inhibitor
2013201311.0low000010
zd 6474aromatic ether;
organobromine compound;
organofluorine compound;
piperidines;
quinazolines;
secondary amine
antineoplastic agent;
tyrosine kinase inhibitor
2013201311.0low000010
compound 968benzophenanthridineEC 3.5.1.2 (glutaminase) inhibitor2013201311.0low000010
sb-2242891,2,4-oxadiazole;
azaspiro compound;
benzamides;
organic heterotetracyclic compound
serotonergic antagonist2013201311.0low000010
gw 7647aryl sulfide;
monocarboxylic acid;
ureas
PPARalpha agonist2013201311.0low000010
l 663536aryl sulfide;
indoles;
monocarboxylic acid;
monochlorobenzenes
antineoplastic agent;
EC 1.13.11.34 (arachidonate 5-lipoxygenase) inhibitor;
leukotriene antagonist
2013201311.0low000010
1-[6-(4-chlorophenyl)-5-imidazo[2,1-b]thiazolyl]-N-[(3,4-dichlorophenyl)methoxy]methanimineimidazoles2013201311.0medium000010
N4-ethyl-N6,1,2-trimethyl-N4-phenylpyrimidin-1-ium-4,6-diaminearomatic amine;
tertiary amino compound
2013201311.0medium000010
2-[[2-[2-(2,3-dihydro-1,4-benzodioxin-6-ylamino)-2-oxoethyl]-1-oxo-5-isoquinolinyl]oxy]propanoic acid ethyl esterisoquinolines2013201311.0low000010
sch 79797quinazolines2013201311.0low000010
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1h-imidazol-2-yl)benzamidebenzamides;
benzodioxoles;
imidazoles;
pyridines
EC 2.7.10.1 (receptor protein-tyrosine kinase) inhibitor2013201311.0low000010
1-(4-Fluorophenyl)-3-(3-(4-fluorophenyl)-3-hydroxypropyl)-4-(4-hydroxyphenyl)azetidin-2-onemonobactam2013201311.0medium000010
imd 0354benzamides2013201311.0low000010
ex 527carbazoles;
monocarboxylic acid amide;
organochlorine compound
2013201311.0low000010
ku 55933201620225.4low000041
quercetin7-hydroxyflavonol;
pentahydroxyflavone
antibacterial agent;
antineoplastic agent;
antioxidant;
Aurora kinase inhibitor;
chelator;
EC 1.10.99.2 [ribosyldihydronicotinamide dehydrogenase (quinone)] inhibitor;
geroprotector;
phytoestrogen;
plant metabolite;
protein kinase inhibitor;
radical scavenger
2013201311.0low000010
genistein7-hydroxyisoflavonesantineoplastic agent;
EC 5.99.1.3 [DNA topoisomerase (ATP-hydrolysing)] inhibitor;
geroprotector;
human urinary metabolite;
phytoestrogen;
plant metabolite;
tyrosine kinase inhibitor
2013201311.0low000010
fenretinidemonocarboxylic acid amide;
retinoid
antineoplastic agent;
antioxidant
2013201311.0low000010
ter 1992013201311.0low000010
arachidonylcyclopropylamide2013201311.0low000010
ly 320135benzofurans2013201311.0low000010
pd 166285201320207.5low000020
kn 62piperazines2013201311.0low000010
su 66562013201311.0low000010
semaxinibolefinic compound;
oxindoles;
pyrroles
angiogenesis modulating agent;
antineoplastic agent;
EC 2.7.10.1 (receptor protein-tyrosine kinase) inhibitor;
vascular endothelial growth factor receptor antagonist
2013201311.0low000010
su 11248monocarboxylic acid amide;
pyrroles
angiogenesis inhibitor;
antineoplastic agent;
EC 2.7.10.1 (receptor protein-tyrosine kinase) inhibitor;
immunomodulator;
neuroprotective agent;
vascular endothelial growth factor receptor antagonist
2013201311.0low000010
palbociclibaminopyridine;
aromatic ketone;
cyclopentanes;
piperidines;
pyridopyrimidine;
secondary amino compound;
tertiary amino compound
antineoplastic agent;
EC 2.7.11.22 (cyclin-dependent kinase) inhibitor
2013201311.0low000010
jnj-7706621sulfonamide2013201311.0low000010
cisplatindiamminedichloroplatinumantineoplastic agent;
apoptosis inducer;
cross-linking reagent;
ferroptosis inducer;
genotoxin;
mutagen;
nephrotoxin;
photosensitizing agent
2013201311.0low000010
vx680N-arylpiperazine2013201311.0low000010
d 4476imidazoles2013201311.0low000010
cyc 1162013201311.0low000010
bay 19-80042013201311.0low000010
axitinibaryl sulfide;
benzamides;
indazoles;
pyridines
antineoplastic agent;
tyrosine kinase inhibitor;
vascular endothelial growth factor receptor antagonist
2013201311.0low000010
pai 039indole-3-acetic acids2013201311.0low000010
gw2974pyridopyrimidine2013201311.0low000010
ispinesibbenzamides2013201311.0low000010
temsirolimusmacrolide lactam2013201311.0low000010
pd 184352aminobenzoic acid2013201311.0low000010
bibx 1382bssubstituted aniline2013201311.0low000010
hdac-42amidobenzoic acid2013201311.0low000010
[4-[[4-(1-benzothiophen-2-yl)-2-pyrimidinyl]amino]phenyl]-[4-(1-pyrrolidinyl)-1-piperidinyl]methanonebenzamides;
N-acylpiperidine
2013201311.0low000010
iniparibcarbonyl compound;
organohalogen compound
2013201311.0low000010
mk 07522013201311.0low000010
gw 5015161,3-thiazoles;
aromatic ether;
aryl sulfide;
monocarboxylic acid;
organofluorine compound
carcinogenic agent;
PPARbeta/delta agonist
2013201311.0low000010
av 4122013201311.0low000010
ag-041r2013201311.0low000010
telatinib2013201311.0low000010
cp 5476322013201311.0low000010
spc-8392013201311.0low000010
lenvatinibaromatic amide;
aromatic ether;
cyclopropanes;
monocarboxylic acid amide;
monochlorobenzenes;
phenylureas;
quinolines
antineoplastic agent;
EC 2.7.10.1 (receptor protein-tyrosine kinase) inhibitor;
fibroblast growth factor receptor antagonist;
orphan drug;
vascular endothelial growth factor receptor antagonist
2013201311.0low000010
andarineacetamides;
anilide
2013201311.0low000010
gw843682x(trifluoromethyl)benzenes2013201311.0low000010
pd 0325901difluorobenzene;
hydroxamic acid ester;
monofluorobenzenes;
organoiodine compound;
propane-1,2-diols;
secondary amino compound
antineoplastic agent;
EC 2.7.12.2 (mitogen-activated protein kinase kinase) inhibitor
2013201311.0low000010
midostaurinbenzamides;
gamma-lactam;
indolocarbazole;
organic heterooctacyclic compound
antineoplastic agent;
EC 2.7.11.13 (protein kinase C) inhibitor
2013201311.0low000010
ag 14361benzimidazoles2013201311.0low000010
sb 2656102013201311.0low000010
fr 148083aromatic ether;
macrolide;
phenols;
secondary alcohol;
secondary alpha-hydroxy ketone
antibacterial agent;
antineoplastic agent;
metabolite;
NF-kappaB inhibitor
2013201311.0low000010
mocetinostataminopyrimidine;
benzamides;
pyridines;
secondary amino compound;
secondary carboxamide;
substituted aniline
antineoplastic agent;
apoptosis inducer;
autophagy inducer;
cardioprotective agent;
EC 3.5.1.98 (histone deacetylase) inhibitor;
hepatotoxic agent
2013201311.0low000010
osi 930aromatic amide2013201311.0low000010
ki 202272013201311.0low000010
scio-469aromatic amide;
aromatic ketone;
chloroindole;
dicarboxylic acid diamide;
indolecarboxamide;
monofluorobenzenes;
N-acylpiperazine;
N-alkylpiperazine
antineoplastic agent;
apoptosis inducer;
EC 2.7.11.24 (mitogen-activated protein kinase) inhibitor
2013201311.0low000010
ssr 69071pyridopyrimidine2013201311.0low000010
pi103aromatic amine;
morpholines;
organic heterotricyclic compound;
phenols;
tertiary amino compound
antineoplastic agent;
EC 2.7.1.137 (phosphatidylinositol 3-kinase) inhibitor;
mTOR inhibitor
2013201311.0low000010
sb 2103132013201311.0high000010
gw 4064stilbenoid2013201311.0low000010
sa 45032013201311.0low000010
ic 871146-aminopurines;
biaryl;
quinazolines
EC 2.7.1.137 (phosphatidylinositol 3-kinase) inhibitor2013201311.0low000010
zibotentanphenylpyridine2013201311.0low000010
tivozanibaromatic ether2013201311.0low000010
hki 272nitrile;
quinolines
antineoplastic agent;
tyrosine kinase inhibitor
2013201311.0low000010
tofacitinibN-acylpiperidine;
nitrile;
pyrrolopyrimidine;
tertiary amino compound
antirheumatic drug;
EC 2.7.10.2 (non-specific protein-tyrosine kinase) inhibitor
2013201311.0low000010
bibr 15322013201311.0low000010
n-(6-chloro-7-methoxy-9h-beta-carbolin-8-yl)-2-methylnicotinamide2013201311.0low000010
rucaparibazepinoindole;
caprolactams;
organofluorine compound;
secondary amino compound
antineoplastic agent;
EC 2.4.2.30 (NAD(+) ADP-ribosyltransferase) inhibitor
2013201311.0low000010
cediranibaromatic ether2013201311.0low000010
gw0742monocarboxylic acid2013201311.0low000010
ps1145beta-carbolines2013201311.0low000010
bay 41-8543pyrazolopyridine2013201311.0low000010
chir 99021aminopyridine;
aminopyrimidine;
cyanopyridine;
diamine;
dichlorobenzene;
imidazoles;
secondary amino compound
EC 2.7.11.26 (tau-protein kinase) inhibitor2013201311.0low000010
sb 525334quinoxaline derivative2013201311.0low000010
way-362450indoles2013201311.0low000010
masitinib1,3-thiazoles;
benzamides;
N-alkylpiperazine;
pyridines
antineoplastic agent;
antirheumatic drug;
tyrosine kinase inhibitor
2013201311.0low000010
bx795ureas2013201311.0low000010
pazopanibaminopyrimidine;
indazoles;
sulfonamide
angiogenesis modulating agent;
antineoplastic agent;
tyrosine kinase inhibitor;
vascular endothelial growth factor receptor antagonist
2013201311.0low000010
sepantroniumorganic cation2013201311.0low000010
azd 6244benzimidazoles;
bromobenzenes;
hydroxamic acid ester;
monochlorobenzenes;
organofluorine compound;
secondary amino compound
anticoronaviral agent;
antineoplastic agent;
EC 2.7.11.24 (mitogen-activated protein kinase) inhibitor
2013201311.0low000010
1-(2-(1-adamantyl)ethyl)-1-pentyl-3-(3-(4-pyridyl)propyl)urea2013201311.0low000010
N-(3-cyanophenyl)-2'-methyl-5'-(5-methyl-1,3,4-oxadiazol-2-yl)biphenyl-4-carboxamide1,3,4-oxadiazoles;
benzamides;
biphenyls;
nitrile
EC 2.7.11.24 (mitogen-activated protein kinase) inhibitor2013201311.0medium000010
ar c1558582013201311.0low000010
aee 7886-{4-[(4-ethylpiperazin-1-yl)methyl]phenyl}-N-(1-phenylethyl)-7H-pyrrolo[2,3-d]pyrimidin-4-amineangiogenesis inhibitor;
antineoplastic agent;
apoptosis inducer;
EC 2.7.10.1 (receptor protein-tyrosine kinase) inhibitor;
epidermal growth factor receptor antagonist;
trypanocidal drug
2013201311.0low000010
saracatinibaromatic ether;
benzodioxoles;
diether;
N-methylpiperazine;
organochlorine compound;
oxanes;
quinazolines;
secondary amino compound
anticoronaviral agent;
antineoplastic agent;
apoptosis inducer;
autophagy inducer;
EC 2.7.10.2 (non-specific protein-tyrosine kinase) inhibitor;
radiosensitizing agent
2013201311.0low000010
sd-2082013201311.0low000010
vx 702phenylpyridine2013201311.0low000010
volasertib2013201311.0low000010
PB28aromatic ether;
piperazines;
tetralins
anticoronaviral agent;
antineoplastic agent;
apoptosis inducer;
sigma-2 receptor agonist
2013201311.0low000010
azd 7762aromatic amide;
thiophenes
2013201311.0low000010
krp-2032013201311.0low000010
mk 03542013201311.0low000010
regorafenib(trifluoromethyl)benzenes;
aromatic ether;
monochlorobenzenes;
monofluorobenzenes;
phenylureas;
pyridinecarboxamide
antineoplastic agent;
hepatotoxic agent;
tyrosine kinase inhibitor
2013201311.0low000010
acetic acid 2-[4-methyl-8-(4-morpholinylsulfonyl)-1,3-dioxo-2-pyrrolo[3,4-c]quinolinyl]ethyl esterpyrroloquinoline2013201311.0low000010
6-[[5-fluoro-2-(3,4,5-trimethoxyanilino)-4-pyrimidinyl]amino]-2,2-dimethyl-4H-pyrido[3,2-b][1,4]oxazin-3-onemethoxybenzenes;
substituted aniline
2013201311.0low000010
brivanibaromatic ether;
diether;
fluoroindole;
pyrrolotriazine;
secondary alcohol
angiogenesis inhibitor;
antineoplastic agent;
apoptosis inducer;
drug metabolite;
EC 2.7.10.1 (receptor protein-tyrosine kinase) inhibitor;
fibroblast growth factor receptor antagonist
2013201311.0low000010
icg 001peptide2013201311.0low000010
mp470N-arylpiperazine2013201311.0low000010
nu 7441dibenzothiophenes201320198.0low000020
at 7519dichlorobenzene;
piperidines;
pyrazoles;
secondary carboxamide
antineoplastic agent;
EC 2.7.11.22 (cyclin-dependent kinase) inhibitor
2013201311.0low000010
bi 25362013201311.0low000010
danusertibpiperazines2013201311.0low000010
N-[4-(2-tert-butylphenyl)sulfonylphenyl]-2,3,4-trihydroxy-5-[(2-propan-2-ylphenyl)methyl]benzamidebenzamides2013201311.0low000010
N-[5-[[5-[(4-acetyl-1-piperazinyl)-oxomethyl]-4-methoxy-2-methylphenyl]thio]-2-thiazolyl]-4-[(3,3-dimethylbutan-2-ylamino)methyl]benzamidebenzamides2013201311.0low000010
abt 869aromatic amine;
indazoles;
phenylureas
angiogenesis inhibitor;
antineoplastic agent;
EC 2.7.10.1 (receptor protein-tyrosine kinase) inhibitor
2013201311.0low000010
dorsomorphinaromatic ether;
piperidines;
pyrazolopyrimidine;
pyridines
bone morphogenetic protein receptor antagonist;
EC 2.7.11.31 {[hydroxymethylglutaryl-CoA reductase (NADPH)] kinase} inhibitor
2013201311.0low000010
ac 2610662013201311.0low000010
carfilzomibepoxide;
morpholines;
tetrapeptide
antineoplastic agent;
proteasome inhibitor
2013201311.0low000010
gw9508aromatic amine2013201311.0low000010
jnj 268541652013201311.0low000010
pf 573228quinolines2013201311.0low000010
gw 25802013201311.0low000010
idelalisibaromatic amine;
organofluorine compound;
purines;
quinazolines;
secondary amino compound
antineoplastic agent;
apoptosis inducer;
EC 2.7.1.137 (phosphatidylinositol 3-kinase) inhibitor
2013201311.0low000010
crizotinib3-[1-(2,6-dichloro-3-fluorophenyl)ethoxy]-5-[1-(piperidin-4-yl)pyrazol-4-yl]pyridin-2-amineantineoplastic agent;
biomarker;
EC 2.7.10.1 (receptor protein-tyrosine kinase) inhibitor
2013201311.0low000010
5-(5,6-dimethoxy-1-benzimidazolyl)-3-[(2-methylsulfonylphenyl)methoxy]-2-thiophenecarbonitrilebenzimidazoles2013201311.0low000010
4-[2-(2-chloro-4-fluoroanilino)-5-methyl-4-pyrimidinyl]-N-[(1S)-1-(3-chlorophenyl)-2-hydroxyethyl]-1H-pyrrole-2-carboxamidearomatic amide;
heteroarene
2013201311.0low000010
osi 906cyclobutanes;
quinolines
2013201311.0low000010
ly21097612013201311.0low000010
chir-265aromatic ether2013201311.0low000010
motesanibpyridinecarboxamide2013201311.0low000010
az-628benzamides2013201311.0low000010
trametinibacetamides;
aromatic amine;
cyclopropanes;
organofluorine compound;
organoiodine compound;
pyridopyrimidine;
ring assembly
anticoronaviral agent;
antineoplastic agent;
EC 2.7.11.24 (mitogen-activated protein kinase) inhibitor;
geroprotector
2013201311.0low000010
pf-562,271indoles2013201311.0low000010
veliparibbenzimidazolesEC 2.4.2.30 (NAD(+) ADP-ribosyltransferase) inhibitor2013201311.0low000010
ku-0060648dibenzothiophenes2013201311.0low000010
dactolisibimidazoquinoline;
nitrile;
quinolines;
ring assembly;
ureas
antineoplastic agent;
EC 2.7.1.137 (phosphatidylinositol 3-kinase) inhibitor;
mTOR inhibitor
201320169.5low000020
palomid 5292013201311.0low000010
tosedostatcarboxylic ester;
hydroxamic acid;
secondary carboxamide
2013201311.0low000010
mdv 3100(trifluoromethyl)benzenes;
benzamides;
imidazolidinone;
monofluorobenzenes;
nitrile;
thiocarbonyl compound
androgen antagonist;
antineoplastic agent
2013201311.0low000010
ku 60019201320226.0high000021
gsk 461364(trifluoromethyl)benzenes2013201311.0low000010
n-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxyphenyl)-1-(2,3-dihydroxypropyl)cyclopropane-1-sulfonamide2013201311.0low000010
nvp-tae684piperidines2013201311.0low000010
4-methyl-3-(2-(2-morpholinoethylamino)quinazolin-6-yl)-n-(3-(trifluoromethyl)phenyl)benzamide2013201311.0medium000010
gsk 269962a2013201311.0low000010
a-83-012013201311.0low000010
3-[(1-methyl-3-indolyl)methylidene]-1H-pyrrolo[3,2-b]pyridin-2-oneindoles2013201311.0medium000010
vx-770aromatic amide;
monocarboxylic acid amide;
phenols;
quinolone
CFTR potentiator;
orphan drug
2013201311.0low000010
buparlisibaminopyridine;
aminopyrimidine;
morpholines;
organofluorine compound
antineoplastic agent;
EC 2.7.1.137 (phosphatidylinositol 3-kinase) inhibitor
2013201311.0low000010
azd 14802013201311.0low000010
fedratinibsulfonamide2013201311.0low000010
gsk6906931,2,5-oxadiazole;
acetylenic compound;
aromatic amine;
aromatic ether;
imidazopyridine;
piperidines;
primary amino compound;
tertiary alcohol
antineoplastic agent;
EC 2.7.11.1 (non-specific serine/threonine protein kinase) inhibitor
2013201311.0low000010
cnf 20242-aminopurines;
aromatic ether;
organochlorine compound;
pyridines
antineoplastic agent;
Hsp90 inhibitor
2013201311.0low000010
ku 0063794benzyl alcohols;
monomethoxybenzene;
morpholines;
pyridopyrimidine;
tertiary amino compound
antineoplastic agent;
mTOR inhibitor
2013201311.0low000010
azd 7545benzamides;
monochlorobenzenes;
organofluorine compound;
secondary carboxamide;
sulfone;
tertiary alcohol;
tertiary carboxamide
EC 2.7.11.2 - [pyruvate dehydrogenase (acetyl-transferring)] kinase inhibitor;
hypoglycemic agent
2013201311.0low000010
nutlin-3bNutlin;
piperazinone
anticoronaviral agent2013201311.0low000010
pf 04217903quinolines2013201311.0low000010
gdc 0941indazoles;
morpholines;
piperazines;
sulfonamide;
thienopyrimidine
EC 2.7.1.137 (phosphatidylinositol 3-kinase) inhibitor2013201311.0low000010
sm 164benzenes;
organic heterobicyclic compound;
secondary carboxamide;
triazoles
antineoplastic agent;
apoptosis inducer;
radiosensitizing agent
2013201311.0low000010
ph 797804aromatic ether;
benzamides;
organobromine compound;
organofluorine compound;
pyridone
anti-inflammatory agent;
EC 2.7.11.24 (mitogen-activated protein kinase) inhibitor
2013201311.0low000010
pha 4082013201311.0low000010
gsk 1016790a1-benzothiophenes;
aromatic primary alcohol;
dichlorobenzene;
N-acylpiperazine;
sulfonamide;
tertiary carboxamide
TRPV4 agonist2013201311.0low000010
olaparibcyclopropanes;
monofluorobenzenes;
N-acylpiperazine;
phthalazines
antineoplastic agent;
apoptosis inducer;
EC 2.4.2.30 (NAD(+) ADP-ribosyltransferase) inhibitor
2013201311.0low000010
srt17202013201311.0low000010
plx 4720aromatic ketone;
difluorobenzene;
organochlorine compound;
pyrrolopyridine;
sulfonamide
antineoplastic agent;
B-Raf inhibitor
2013201311.0low000010
cx 49452013201311.0low000010
cudc 1012013201311.0low000010
mln 8237benzazepine2013201311.0low000010
lde225aminopyridine;
aromatic ether;
benzamides;
biphenyls;
morpholines;
organofluorine compound;
tertiary amino compound
antineoplastic agent;
Hedgehog signaling pathway inhibitor;
SMO receptor antagonist
2013201311.0low000010
gdc 0449benzamides;
monochlorobenzenes;
pyridines;
sulfone
antineoplastic agent;
Hedgehog signaling pathway inhibitor;
SMO receptor antagonist;
teratogenic agent
2013201311.0low000010
sgx 523aryl sulfide;
biaryl;
pyrazoles;
quinolines;
triazolopyridazine
c-Met tyrosine kinase inhibitor;
nephrotoxic agent
2013201311.0low000010
bms 777607aromatic amide2013201311.0low000010
sgi 1776imidazoles2013201311.0low000010
pci 32765acrylamides;
aromatic amine;
aromatic ether;
N-acylpiperidine;
pyrazolopyrimidine;
tertiary carboxamide
antineoplastic agent;
EC 2.7.10.2 (non-specific protein-tyrosine kinase) inhibitor
2013201311.0low000010
ponatinib(trifluoromethyl)benzenes;
acetylenic compound;
benzamides;
imidazopyridazine;
N-methylpiperazine
antineoplastic agent;
tyrosine kinase inhibitor
2013201311.0low000010
amg 9002013201311.0low000010
mk-1775piperazines201320207.5low000020
bag9562013201311.0low000010
quizartinibbenzoimidazothiazole;
isoxazoles;
morpholines;
phenylureas
antineoplastic agent;
EC 2.7.10.1 (receptor protein-tyrosine kinase) inhibitor;
necroptosis inhibitor
2013201311.0low000010
N-[4-[3-[[[7-(hydroxyamino)-7-oxoheptyl]amino]-oxomethyl]-5-isoxazolyl]phenyl]carbamic acid tert-butyl estercarbamate ester2013201311.0low000010
tak 7332013201311.0low000010
mk 2206organic heterotricyclic compoundEC 2.7.1.137 (phosphatidylinositol 3-kinase) inhibitor2013201311.0low000010
navitoclaxaryl sulfide;
monochlorobenzenes;
morpholines;
N-sulfonylcarboxamide;
organofluorine compound;
piperazines;
secondary amino compound;
sulfone;
tertiary amino compound
antineoplastic agent;
apoptosis inducer;
B-cell lymphoma 2 inhibitor
2013201311.0low000010
sns 314ureas2013201311.0low000010
jzl 184benzodioxoles2013201311.0low000010
n-(cyanomethyl)-4-(2-((4-(4-morpholinyl)phenyl)amino)-4-pyrimidinyl)benzamideaminopyrimidine;
benzamides;
morpholines;
nitrile;
secondary amino compound;
tertiary amino compound
anti-anaemic agent;
antineoplastic agent;
apoptosis inducer;
EC 2.7.10.2 (non-specific protein-tyrosine kinase) inhibitor
2013201311.0low000010
dcc-2036organofluorine compound;
phenylureas;
pyrazoles;
pyridinecarboxamide;
quinolines
tyrosine kinase inhibitor2013201311.0low000010
cabozantinibaromatic ether;
dicarboxylic acid diamide;
organofluorine compound;
quinolines
antineoplastic agent;
tyrosine kinase inhibitor
2013201311.0low000010
N-(2,6-difluorophenyl)-5-[3-[2-[5-ethyl-2-methoxy-4-[4-(4-methylsulfonyl-1-piperazinyl)-1-piperidinyl]anilino]-4-pyrimidinyl]-2-imidazo[1,2-a]pyridinyl]-2-methoxybenzamidebenzamides2013201311.0low000010
incb-018424nitrile;
pyrazoles;
pyrrolopyrimidine
antineoplastic agent;
EC 2.7.10.2 (non-specific protein-tyrosine kinase) inhibitor
2013201311.0low000010
bix 01294piperidines2013201311.0low000010
pf 3845piperidines2013201311.0low000010
gsk 2126458aromatic ether;
difluorobenzene;
pyridazines;
pyridines;
quinolines;
sulfonamide
anticoronaviral agent;
antineoplastic agent;
autophagy inducer;
EC 2.7.1.137 (phosphatidylinositol 3-kinase) inhibitor;
mTOR inhibitor;
radiosensitizing agent
2013201311.0low000010
ixazomibbenzamides;
boronic acids;
dichlorobenzene;
glycine derivative
antineoplastic agent;
apoptosis inducer;
drug metabolite;
orphan drug;
proteasome inhibitor
2013201311.0low000010
ldn 193189pyrimidines2013201311.0low000010
plx4032aromatic ketone;
difluorobenzene;
monochlorobenzenes;
pyrrolopyridine;
sulfonamide
antineoplastic agent;
B-Raf inhibitor
2013201311.0low000010
(2S)-2-[[2-(2,3-dihydro-1H-inden-5-yloxy)-9-[(4-phenylphenyl)methyl]-6-purinyl]amino]-3-phenyl-1-propanolbiphenyls2013201311.0low000010
gsk 1363089aromatic ether2013201311.0low000010
kin-193pyridopyrimidine2013201311.0low000010
bay 8697662013201311.0low000010
4-[6-[4-(methoxycarbonylamino)phenyl]-4-(4-morpholinyl)-1-pyrazolo[3,4-d]pyrimidinyl]-1-piperidinecarboxylic acid methyl estercarbamate ester2013201311.0low000010
6-[(3-aminophenyl)methyl]-4-methyl-2-methylsulfinyl-5-thieno[3,4]pyrrolo[1,3-d]pyridazinoneorganic heterobicyclic compound;
organonitrogen heterocyclic compound;
organosulfur heterocyclic compound
2013201311.0low000010
3-[[4-(2,3-dihydro-1,4-benzodioxin-6-ylsulfonyl)-1,4-diazepan-1-yl]sulfonyl]anilinebenzenes;
sulfonamide
2013201311.0low000010
CAY10626ureas2013201311.0medium000010
thiopental sodiumorganochlorine compound;
piperazines;
pyrimidines
antineoplastic agent;
tyrosine kinase inhibitor
2013201311.0low000010
pha 793887piperidinecarboxamide2013201311.0low000010
nvp-bsk8052013201311.0low000010
xmd 8-92pyrimidobenzodiazepineprotein kinase inhibitor2013201311.0low000010
jq1 compoundcarboxylic ester;
organochlorine compound;
tert-butyl ester;
thienotriazolodiazepine
angiogenesis inhibitor;
anti-inflammatory agent;
antineoplastic agent;
apoptosis inducer;
bromodomain-containing protein 4 inhibitor;
cardioprotective agent;
ferroptosis inducer
2013201311.0low000010
jnj38877605quinolines2013201311.0low000010
N-[3-(1,3-benzothiazol-2-yl)-5,6-dihydro-4H-thieno[2,3-c]pyrrol-2-yl]acetamidebenzothiazoles2013201311.0medium000010
dinaciclibpyrazolopyrimidine202020204.0low000010
torin 1N-acylpiperazine;
N-arylpiperazine;
organofluorine compound;
pyridoquinoline;
quinolines
antineoplastic agent;
mTOR inhibitor
2013201311.0low000010
ly29406802013201311.0low000010
1-[4-fluoro-3-(trifluoromethyl)phenyl]-3-(5-pyridin-4-yl-1,3,4-thiadiazol-2-yl)ureaureas2013201311.0low000010
ro 4929097dibenzoazepine;
dicarboxylic acid diamide;
lactam;
organofluorine compound
EC 3.4.23.46 (memapsin 2) inhibitor2013201311.0medium000010
gsk41122013201311.0low000010
torin 2aminopyridine;
organofluorine compound;
primary amino compound;
pyridoquinoline
antineoplastic agent;
mTOR inhibitor
2013201311.0low000010
pf-47086712013201311.0low000010
N-[4-(1-benzoyl-4-piperidinyl)butyl]-3-(3-pyridinyl)-2-propenamidebenzamides;
N-acylpiperidine
2013201311.0medium000010
2-methoxy-N-[3-[4-[3-methyl-4-[(6-methyl-3-pyridinyl)oxy]anilino]-6-quinazolinyl]prop-2-enyl]acetamidearomatic ether;
methylpyridines;
olefinic compound;
quinazolines;
secondary amino compound;
secondary carboxamide;
toluenes
2013201311.0medium000010
belinostatolefinic compound2013201311.0medium000010
ethyl 1-benzyl-3-hydroxy-2(5h)-oxopyrrole-4-carboxylatecarboxylic acid;
pyrroline
2013201311.0low000010
a 769662biphenyls2013201311.0low000010
LimKi 31,3-thiazoles;
dichlorobenzene;
organofluorine compound;
pyrazoles;
secondary carboxamide
LIM kinase inhibitor2013201311.0low000010
1-[4-amino-7-[3-(2-methoxyethylamino)propyl]-5-(4-methylphenyl)-6-pyrrolo[2,3-d]pyrimidinyl]-2-fluoroethanonepyrroles2013201311.0medium000010
2-[5-[(3,5-dimethyl-1H-pyrrol-2-yl)methylidene]-4-methoxy-2-pyrrolylidene]indoledipyrrins2013201311.0medium000010
N-hydroxy-3-[4-[[2-(2-methyl-1H-indol-3-yl)ethylamino]methyl]phenyl]-2-propenamidetryptamines2013201311.0medium000010
3-[(5-tert-butyl-1H-imidazol-4-yl)methylidene]-6-(phenylmethylene)piperazine-2,5-dionepyrazines2013201311.0medium000010
gsk837149a2013201311.0low000010
N-[4-(3-chloro-4-fluoroanilino)-7-[[(3S)-3-oxolanyl]oxy]-6-quinazolinyl]-4-(dimethylamino)-2-butenamidequinazolines2013201311.0medium000010
N-[4-(3-chloro-4-fluoroanilino)-7-methoxy-6-quinazolinyl]-4-(1-piperidinyl)-2-butenamidequinazolines2013201311.0medium000010
wnt-c592013201311.0low000010
5-[1-(2-hydroxyethyl)-3-pyridin-4-yl-4-pyrazolyl]-2,3-dihydroinden-1-one oximeindanes2013201311.0medium000010
sar405201920195.0low000010
THZ531aminopyrimidine;
enamide;
indoles;
N-acylpiperidine;
organochlorine compound;
secondary amino compound;
secondary carboxamide
antineoplastic agent;
apoptosis inducer;
EC 2.7.11.22 (cyclin-dependent kinase) inhibitor
202020204.0low000010
chir 2582013201311.0low000010
osi 0272013201311.0low000010
hli 3732013201311.0medium000010
pemetrexedN-acyl-L-glutamic acid;
pyrrolopyrimidine
antimetabolite;
antineoplastic agent;
EC 1.5.1.3 (dihydrofolate reductase) inhibitor;
EC 2.1.1.45 (thymidylate synthase) inhibitor;
EC 2.1.2.2 (phosphoribosylglycinamide formyltransferase) inhibitor
2013201311.0low000010
sildenafil citratecitrate saltEC 3.1.4.35 (3',5'-cyclic-GMP phosphodiesterase) inhibitor;
vasodilator agent
2013201311.0low000010
aprepitant(trifluoromethyl)benzenes;
cyclic acetal;
morpholines;
triazoles
antidepressant;
antiemetic;
neurokinin-1 receptor antagonist;
peripheral nervous system drug;
substance P receptor antagonist
2013201311.0low000010
xav939(trifluoromethyl)benzenes;
thiopyranopyrimidine
tankyrase inhibitor2013201311.0low000010
2-carboxyarabinitol 1-phosphate2013201311.0low000010
nintedanib2013201311.0low000010
ver 52296aromatic amide;
isoxazoles;
monocarboxylic acid amide;
morpholines;
resorcinols
angiogenesis inhibitor;
antineoplastic agent;
Hsp90 inhibitor
2013201311.0low000010
sb-590885aromatic ether;
imidazoles;
ketoxime;
pyridines;
tertiary amino compound
2013201311.0medium000010
pf-4777362013201311.0low000010
fenobamureas2013201311.0low000010
ConditionIndicatedStudiesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
Akinetic-Rigid Variant of Huntington Disease0201920195.0low000010
Ataxia Telangiectasia0202220222.0low000001
Ataxia Telangiectasia Syndrome0202220222.0low000001
Benign Neoplasms0202020223.0medium000011
Congenital Zika Syndrome0202020204.0low000010
Disease Models, Animal0201920204.5medium000020
Experimental Neoplasms0201620168.0low000010
Huntington Disease0201920195.0low000010
Malaria, Falciparum02014201410.0low000010
Neoplasms0202020223.0medium000011
Plasmodium falciparum Malaria02014201410.0low000010
Zika Virus Infection0202020204.0low000010

Bioavailability (2)

ArticleYear
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
Molecular pharmacology, , Volume: 96, Issue:5
2019
Discovery of Novel 3-Quinoline Carboxamides as Potent, Selective, and Orally Bioavailable Inhibitors of Ataxia Telangiectasia Mutated (ATM) Kinase.
Journal of medicinal chemistry, , 07-14, Volume: 59, Issue:13
2016