Assay ID | Title | Year | Journal | Article |
AID1595620 | Inhibition of EGFR in human A431 cells assessed as reduction in EGF-stimulated EGFR autophosphorylation preincuabted for 90 mins followed by EGF-stimulation by sandwich-ELISA | 2019 | Journal of medicinal chemistry, 05-09, Volume: 62, Issue:9
| Design of a Cyclin G Associated Kinase (GAK)/Epidermal Growth Factor Receptor (EGFR) Inhibitor Set to Interrogate the Relationship of EGFR and GAK in Chordoma. |
AID473322 | Inhibition of EGFR Leu858Arg mutant by HTRF assay | 2010 | Journal of medicinal chemistry, Apr-08, Volume: 53, Issue:7
| Synthesis and biological evaluation of 4-anilinoquinolines as potent inhibitors of epidermal growth factor receptor. |
AID1595640 | Binding affinity to GAK in human SUM159 cell lysates by multiplexed inhibitor bead profiling-based LC-MS/MS analysis | 2019 | Journal of medicinal chemistry, 05-09, Volume: 62, Issue:9
| Design of a Cyclin G Associated Kinase (GAK)/Epidermal Growth Factor Receptor (EGFR) Inhibitor Set to Interrogate the Relationship of EGFR and GAK in Chordoma. |
AID89523 | Concentration required to inhibit the human liver recombinant fructose-1,6-bisphosphatase. | 2001 | Bioorganic & medicinal chemistry letters, Jan-08, Volume: 11, Issue:1
| Allosteric inhibition of fructose-1,6-bisphosphatase by anilinoquinazolines. |
AID1595625 | Antiproliferative activity against human UMCHOR1 cells measured after 72 hrs by alamar blue assay | 2019 | Journal of medicinal chemistry, 05-09, Volume: 62, Issue:9
| Design of a Cyclin G Associated Kinase (GAK)/Epidermal Growth Factor Receptor (EGFR) Inhibitor Set to Interrogate the Relationship of EGFR and GAK in Chordoma. |
AID1589075 | Cytotoxicity in human WS1 cells assessed as reduction in cell viability incubated fro 48 hrs by alamar blue dye based assay | 2019 | Bioorganic & medicinal chemistry letters, 09-15, Volume: 29, Issue:18
| Anti-tubercular activity of novel 4-anilinoquinolines and 4-anilinoquinazolines. |
AID1815407 | Cytotoxicity against DENV infected human Huh-7 cells assessed as reduction in cell viability by alamar blue assay | 2021 | Bioorganic & medicinal chemistry letters, 11-15, Volume: 52 | Identification and evaluation of 4-anilinoquin(az)olines as potent inhibitors of both dengue virus (DENV) and Venezuelan equine encephalitis virus (VEEV). |
AID1589080 | Anti-tubercular activity against Mycobacterium tuberculosis H37Rv expressing LuxABCDE assessed as relative luminescence by measuring ratio of RLU (test compound)/RLU(no compound) at 20 uM by luminescence based assay | 2019 | Bioorganic & medicinal chemistry letters, 09-15, Volume: 29, Issue:18
| Anti-tubercular activity of novel 4-anilinoquinolines and 4-anilinoquinazolines. |
AID1815409 | Cytotoxicity against Venezuelan equine encephalitis virus TC-83 strain infected human U-87 MG cells assessed as reduction in cell viability by alamar blue assay | 2021 | Bioorganic & medicinal chemistry letters, 11-15, Volume: 52 | Identification and evaluation of 4-anilinoquin(az)olines as potent inhibitors of both dengue virus (DENV) and Venezuelan equine encephalitis virus (VEEV). |
AID1595636 | Effect on total EGFR expression in human UCH2 cells at 1 to 10 uM measured after 4 hrs by Western blot analysis | 2019 | Journal of medicinal chemistry, 05-09, Volume: 62, Issue:9
| Design of a Cyclin G Associated Kinase (GAK)/Epidermal Growth Factor Receptor (EGFR) Inhibitor Set to Interrogate the Relationship of EGFR and GAK in Chordoma. |
AID473329 | Growth inhibition of mouse BA/F3 cells expressing EGFR Del3 and Thr790Met mutant after 96 hrs by cell titer-glo assay | 2010 | Journal of medicinal chemistry, Apr-08, Volume: 53, Issue:7
| Synthesis and biological evaluation of 4-anilinoquinolines as potent inhibitors of epidermal growth factor receptor. |
AID1595618 | Binding affinity to wild-type human partial length EGFR (R669 to V1011 residues) expressed in bacterial expression system by Kinomescan method | 2019 | Journal of medicinal chemistry, 05-09, Volume: 62, Issue:9
| Design of a Cyclin G Associated Kinase (GAK)/Epidermal Growth Factor Receptor (EGFR) Inhibitor Set to Interrogate the Relationship of EGFR and GAK in Chordoma. |
AID473327 | Growth inhibition of mouse BA/F3 cells expressing EGFR L858R mutant after 96 hrs by cell titer-glo assay | 2010 | Journal of medicinal chemistry, Apr-08, Volume: 53, Issue:7
| Synthesis and biological evaluation of 4-anilinoquinolines as potent inhibitors of epidermal growth factor receptor. |
AID1815406 | Antiviral activity against DENV2 New Guinea C strain infected in human Huh7 cells assessed as reduction in viral infection measured after 48 hrs post infection by renilla luciferase assay relative to control | 2021 | Bioorganic & medicinal chemistry letters, 11-15, Volume: 52 | Identification and evaluation of 4-anilinoquin(az)olines as potent inhibitors of both dengue virus (DENV) and Venezuelan equine encephalitis virus (VEEV). |
AID1595624 | Antiproliferative activity against human UCH7 cells measured after 72 hrs by alamar blue assay | 2019 | Journal of medicinal chemistry, 05-09, Volume: 62, Issue:9
| Design of a Cyclin G Associated Kinase (GAK)/Epidermal Growth Factor Receptor (EGFR) Inhibitor Set to Interrogate the Relationship of EGFR and GAK in Chordoma. |
AID1595638 | Inhibition of EGFR in human UCH2 cells assessed as reduction in EGF-induced EGFR phosphorylation at Y1068 residue at 10 uM preincubated for 4 hrs followed by EGF--stimulation and measured after 15 mins by Western blot analysis relative to control | 2019 | Journal of medicinal chemistry, 05-09, Volume: 62, Issue:9
| Design of a Cyclin G Associated Kinase (GAK)/Epidermal Growth Factor Receptor (EGFR) Inhibitor Set to Interrogate the Relationship of EGFR and GAK in Chordoma. |
AID1595627 | Antiproliferative activity against human UCH12 cells measured after 72 hrs by alamar blue assay | 2019 | Journal of medicinal chemistry, 05-09, Volume: 62, Issue:9
| Design of a Cyclin G Associated Kinase (GAK)/Epidermal Growth Factor Receptor (EGFR) Inhibitor Set to Interrogate the Relationship of EGFR and GAK in Chordoma. |
AID1595635 | Effect on total EGFR expression in human UCH1 cells at 1 to 10 uM measured after 4 hrs by Western blot analysis | 2019 | Journal of medicinal chemistry, 05-09, Volume: 62, Issue:9
| Design of a Cyclin G Associated Kinase (GAK)/Epidermal Growth Factor Receptor (EGFR) Inhibitor Set to Interrogate the Relationship of EGFR and GAK in Chordoma. |
AID1595626 | Antiproliferative activity against human CH22 cells measured after 72 hrs by alamar blue assay | 2019 | Journal of medicinal chemistry, 05-09, Volume: 62, Issue:9
| Design of a Cyclin G Associated Kinase (GAK)/Epidermal Growth Factor Receptor (EGFR) Inhibitor Set to Interrogate the Relationship of EGFR and GAK in Chordoma. |
AID473325 | Growth inhibition of mouse BA/F3 cells expressing EGFR Del3 mutant after 96 hrs by cell titer-glo assay | 2010 | Journal of medicinal chemistry, Apr-08, Volume: 53, Issue:7
| Synthesis and biological evaluation of 4-anilinoquinolines as potent inhibitors of epidermal growth factor receptor. |
AID1589079 | Anti-tubercular activity against Mycobacterium tuberculosis H37Rv expressing LuxABCDE assessed as relative luminescence by measuring ratio of RLU (test compound)/RLU(no compound) at 10 uM by luminescence based assay | 2019 | Bioorganic & medicinal chemistry letters, 09-15, Volume: 29, Issue:18
| Anti-tubercular activity of novel 4-anilinoquinolines and 4-anilinoquinazolines. |
AID160681 | Compound was evaluated for its concentration required to inhibit the porcine kidney F16BPase | 2001 | Bioorganic & medicinal chemistry letters, Jan-08, Volume: 11, Issue:1
| Allosteric inhibition of fructose-1,6-bisphosphatase by anilinoquinazolines. |
AID195073 | Compound was evaluated for its concentration required to inhibit the rat liver F16BPase | 2001 | Bioorganic & medicinal chemistry letters, Jan-08, Volume: 11, Issue:1
| Allosteric inhibition of fructose-1,6-bisphosphatase by anilinoquinazolines. |
AID1595619 | Binding affinity to wild-type human partial length GAK (G13 to Y338 residues) expressed in bacterial expression system by Kinomescan method | 2019 | Journal of medicinal chemistry, 05-09, Volume: 62, Issue:9
| Design of a Cyclin G Associated Kinase (GAK)/Epidermal Growth Factor Receptor (EGFR) Inhibitor Set to Interrogate the Relationship of EGFR and GAK in Chordoma. |
AID473324 | Growth inhibition of mouse BA/F3 cells expressing EGFR Del1 mutant after 96 hrs by cell titer-glo assay | 2010 | Journal of medicinal chemistry, Apr-08, Volume: 53, Issue:7
| Synthesis and biological evaluation of 4-anilinoquinolines as potent inhibitors of epidermal growth factor receptor. |
AID1595617 | Antiproliferative activity against human UCH2 cells measured after 72 hrs by alamar blue assay | 2019 | Journal of medicinal chemistry, 05-09, Volume: 62, Issue:9
| Design of a Cyclin G Associated Kinase (GAK)/Epidermal Growth Factor Receptor (EGFR) Inhibitor Set to Interrogate the Relationship of EGFR and GAK in Chordoma. |
AID684832 | Inhibition of human recombinant FBPase using fructose-1,6-biphosphate as substrate incubated for 3 mins prior to substrate addition by spectrophotometric analysis | 2012 | European journal of medicinal chemistry, Oct, Volume: 56 | Ligand-based designing, in silico screening, and biological evaluation of new potent fructose-1,6-bisphosphatase (FBPase) inhibitors. |
AID1595621 | Inhibition of tracer 5 binding to human N-terminal nano luciferase-fused GAK expressed in HEK293 cells measured after 2 hrs by nanoBRET assay | 2019 | Journal of medicinal chemistry, 05-09, Volume: 62, Issue:9
| Design of a Cyclin G Associated Kinase (GAK)/Epidermal Growth Factor Receptor (EGFR) Inhibitor Set to Interrogate the Relationship of EGFR and GAK in Chordoma. |
AID1589078 | Anti-tubercular activity against Mycobacterium tuberculosis H37Rv expressing LuxABCDE assessed as relative luminescence by measuring ratio of RLU (test compound)/RLU(no compound) at 5 uM by luminescence based assay | 2019 | Bioorganic & medicinal chemistry letters, 09-15, Volume: 29, Issue:18
| Anti-tubercular activity of novel 4-anilinoquinolines and 4-anilinoquinazolines. |
AID1595644 | Binding affinity to EGFR in human SUM159 cell lysates by multiplexed inhibitor bead profiling-based LC-MS/MS analysis | 2019 | Journal of medicinal chemistry, 05-09, Volume: 62, Issue:9
| Design of a Cyclin G Associated Kinase (GAK)/Epidermal Growth Factor Receptor (EGFR) Inhibitor Set to Interrogate the Relationship of EGFR and GAK in Chordoma. |
AID1815408 | Antiviral activity against Venezuelan equine encephalitis virus TC-83 strain infected in human U-87 MG cells assessed as reduction in viral infection measured after 18 hrs post infection by Nano luciferase assay relative to control | 2021 | Bioorganic & medicinal chemistry letters, 11-15, Volume: 52 | Identification and evaluation of 4-anilinoquin(az)olines as potent inhibitors of both dengue virus (DENV) and Venezuelan equine encephalitis virus (VEEV). |
AID165448 | Compound was evaluated for its concentration required to inhibit the rabbit liver F16BPase | 2001 | Bioorganic & medicinal chemistry letters, Jan-08, Volume: 11, Issue:1
| Allosteric inhibition of fructose-1,6-bisphosphatase by anilinoquinazolines. |
AID1595623 | Cytotoxicity against human WS1 cells measured after 72 hrs by alamar blue assay | 2019 | Journal of medicinal chemistry, 05-09, Volume: 62, Issue:9
| Design of a Cyclin G Associated Kinase (GAK)/Epidermal Growth Factor Receptor (EGFR) Inhibitor Set to Interrogate the Relationship of EGFR and GAK in Chordoma. |
AID473523 | Growth inhibition of mouse BA/F3 cells expressing EGFR L858R and Thr790Met mutant after 96 hrs by cell titer-glo assay | 2010 | Journal of medicinal chemistry, Apr-08, Volume: 53, Issue:7
| Synthesis and biological evaluation of 4-anilinoquinolines as potent inhibitors of epidermal growth factor receptor. |
AID1595615 | Inhibition of EGFR in human UCH1 cells assessed as reduction in EGF-induced EGFR phosphorylation at Y1068 residue at 10 uM preincubated for 4 hrs followed by EGF--stimulation and measured after 15 mins by Western blot analysis relative to control | 2019 | Journal of medicinal chemistry, 05-09, Volume: 62, Issue:9
| Design of a Cyclin G Associated Kinase (GAK)/Epidermal Growth Factor Receptor (EGFR) Inhibitor Set to Interrogate the Relationship of EGFR and GAK in Chordoma. |
AID473321 | Inhibition of wild type EGFR by HTRF assay | 2010 | Journal of medicinal chemistry, Apr-08, Volume: 53, Issue:7
| Synthesis and biological evaluation of 4-anilinoquinolines as potent inhibitors of epidermal growth factor receptor. |
AID473328 | Growth inhibition of mouse BA/F3 cells expressing EGFR Del1 and Thr790Met mutant after 96 hrs by cell titer-glo assay | 2010 | Journal of medicinal chemistry, Apr-08, Volume: 53, Issue:7
| Synthesis and biological evaluation of 4-anilinoquinolines as potent inhibitors of epidermal growth factor receptor. |
AID1773372 | Inhibition of recombinant full length LSD1 (unknown origin) transfected in Escherichia coli BL21 (DE) using H3K4me2 as substrate by flourescence based analysis | | | |
AID1589082 | Anti-tubercular activity against Mycobacterium tuberculosis H37Rv expressing LuxABCDE assessed as luminescence signal at 1.3 uM by luminescence based assay relative to untreated control | 2019 | Bioorganic & medicinal chemistry letters, 09-15, Volume: 29, Issue:18
| Anti-tubercular activity of novel 4-anilinoquinolines and 4-anilinoquinazolines. |
AID473323 | Inhibition of EGFR Leu858Arg and Thr790Met mutant by HTRF assay | 2010 | Journal of medicinal chemistry, Apr-08, Volume: 53, Issue:7
| Synthesis and biological evaluation of 4-anilinoquinolines as potent inhibitors of epidermal growth factor receptor. |
AID473330 | Growth inhibition of mouse BA/F3 cells expressing EGFR Del5 and Thr790Met mutant after 96 hrs by cell titer-glo assay | 2010 | Journal of medicinal chemistry, Apr-08, Volume: 53, Issue:7
| Synthesis and biological evaluation of 4-anilinoquinolines as potent inhibitors of epidermal growth factor receptor. |
AID1595628 | Antiproliferative activity against human UCH14 cells measured after 72 hrs by alamar blue assay | 2019 | Journal of medicinal chemistry, 05-09, Volume: 62, Issue:9
| Design of a Cyclin G Associated Kinase (GAK)/Epidermal Growth Factor Receptor (EGFR) Inhibitor Set to Interrogate the Relationship of EGFR and GAK in Chordoma. |
AID310063 | Inhibition of EGFR | 2007 | Bioorganic & medicinal chemistry letters, Nov-15, Volume: 17, Issue:22
| Synthesis and biological evaluation of substituted 6-alkynyl-4-anilinoquinazoline derivatives as potent EGFR inhibitors. |
AID1595639 | Inhibition of EGFR in human UCH2 cells assessed as reduction in EGF-induced EGFR phosphorylation at Y1068 residue at 1 uM preincubated for 4 hrs followed by EGF--stimulation and measured after 15 mins by Western blot analysis relative to control | 2019 | Journal of medicinal chemistry, 05-09, Volume: 62, Issue:9
| Design of a Cyclin G Associated Kinase (GAK)/Epidermal Growth Factor Receptor (EGFR) Inhibitor Set to Interrogate the Relationship of EGFR and GAK in Chordoma. |
AID1595616 | Antiproliferative activity against human UCH1 cells measured after 72 hrs by alamar blue assay | 2019 | Journal of medicinal chemistry, 05-09, Volume: 62, Issue:9
| Design of a Cyclin G Associated Kinase (GAK)/Epidermal Growth Factor Receptor (EGFR) Inhibitor Set to Interrogate the Relationship of EGFR and GAK in Chordoma. |
AID1595637 | Inhibition of EGFR in human UCH1 cells assessed as reduction in EGF-induced EGFR phosphorylation at Y1068 residue at 1 uM preincubated for 4 hrs followed by EGF--stimulation and measured after 15 mins by Western blot analysis relative to control | 2019 | Journal of medicinal chemistry, 05-09, Volume: 62, Issue:9
| Design of a Cyclin G Associated Kinase (GAK)/Epidermal Growth Factor Receptor (EGFR) Inhibitor Set to Interrogate the Relationship of EGFR and GAK in Chordoma. |
AID473326 | Growth inhibition of mouse BA/F3 cells expressing EGFR Del5 mutant after 96 hrs by cell titer-glo assay | 2010 | Journal of medicinal chemistry, Apr-08, Volume: 53, Issue:7
| Synthesis and biological evaluation of 4-anilinoquinolines as potent inhibitors of epidermal growth factor receptor. |
AID1589083 | Anti-tubercular activity against Mycobacterium tuberculosis H37Rv expressing LuxABCDE assessed as luminescence signal at 2.5 uM by luminescence based assay relative to untreated control | 2019 | Bioorganic & medicinal chemistry letters, 09-15, Volume: 29, Issue:18
| Anti-tubercular activity of novel 4-anilinoquinolines and 4-anilinoquinazolines. |
AID1346987 | P-glycoprotein substrates identified in KB-8-5-11 adenocarcinoma cell line, qHTS therapeutic library screen | 2019 | Molecular pharmacology, 11, Volume: 96, Issue:5
| A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. |
AID1508630 | Primary qHTS for small molecule stabilizers of the endoplasmic reticulum resident proteome: Secreted ER Calcium Modulated Protein (SERCaMP) assay | 2021 | Cell reports, 04-27, Volume: 35, Issue:4
| A target-agnostic screen identifies approved drugs to stabilize the endoplasmic reticulum-resident proteome. |
AID1347154 | Primary screen GU AMC qHTS for Zika virus inhibitors | 2020 | Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
| Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors. |
AID1346986 | P-glycoprotein substrates identified in KB-3-1 adenocarcinoma cell line, qHTS therapeutic library screen | 2019 | Molecular pharmacology, 11, Volume: 96, Issue:5
| A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |