ID Source | ID |
---|---|
PubMed CID | 3237904 |
CHEMBL ID | 1420829 |
CHEBI ID | 93471 |
Synonym |
---|
MLS000089581 , |
smr000027929 |
4-[(1-methyl-2-oxo-1,2-dihydroquinolin-4-yl)oxy]-n-(4-methylpyridin-2-yl)butanamide |
4-(1-methyl-2-oxoquinolin-4-yl)oxy-n-(4-methylpyridin-2-yl)butanamide |
HMS2410A05 |
4-(1-methyl-2-oxidanylidene-quinolin-4-yl)oxy-n-(4-methylpyridin-2-yl)butanamide |
cid_3237904 |
4-[(1-methyl-2-oxo-4-quinolinyl)oxy]-n-(4-methyl-2-pyridinyl)butanamide |
bdbm38959 |
4-[(2-keto-1-methyl-4-quinolyl)oxy]-n-(4-methyl-2-pyridyl)butyramide |
CHEMBL1420829 |
CHEBI:93471 |
Q27165168 |
Class | Description |
---|---|
quinolines | A class of aromatic heterocyclic compounds each of which contains a benzene ring ortho fused to carbons 2 and 3 of a pyridine ring. |
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res] |
Protein | Taxonomy | Measurement | Average (µ) | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
Chain A, JmjC domain-containing histone demethylation protein 3A | Homo sapiens (human) | Potency | 79.4328 | 0.6310 | 35.7641 | 100.0000 | AID504339 |
BRCA1 | Homo sapiens (human) | Potency | 31.6228 | 0.8913 | 7.7225 | 25.1189 | AID624202 |
ATAD5 protein, partial | Homo sapiens (human) | Potency | 29.0929 | 0.0041 | 10.8903 | 31.5287 | AID504467 |
TDP1 protein | Homo sapiens (human) | Potency | 26.1011 | 0.0008 | 11.3822 | 44.6684 | AID686978; AID686979 |
Smad3 | Homo sapiens (human) | Potency | 22.3872 | 0.0052 | 7.8098 | 29.0929 | AID588855 |
bromodomain adjacent to zinc finger domain 2B | Homo sapiens (human) | Potency | 89.1251 | 0.7079 | 36.9043 | 89.1251 | AID504333 |
P53 | Homo sapiens (human) | Potency | 56.2341 | 0.0731 | 9.6858 | 31.6228 | AID504706 |
hepatitis C virus polyprotein | Potency | 7.9053 | 0.4445 | 10.4371 | 24.9988 | AID720575 | |
heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa) | Homo sapiens (human) | Potency | 4.4668 | 0.0165 | 25.3078 | 41.3999 | AID602332 |
NPC intracellular cholesterol transporter 1 precursor | Homo sapiens (human) | Potency | 5.6234 | 0.0126 | 2.4518 | 25.0177 | AID485313 |
hemoglobin subunit beta | Homo sapiens (human) | Potency | 2.0812 | 0.3162 | 9.0861 | 31.6228 | AID1405; AID925 |
chromobox protein homolog 1 | Homo sapiens (human) | Potency | 89.1251 | 0.0060 | 26.1688 | 89.1251 | AID540317 |
nuclear factor erythroid 2-related factor 2 isoform 2 | Homo sapiens (human) | Potency | 4.9571 | 0.0041 | 9.9848 | 25.9290 | AID504444; AID720524 |
huntingtin isoform 2 | Homo sapiens (human) | Potency | 1.7783 | 0.0006 | 18.4198 | 1,122.0200 | AID1688 |
nuclear receptor ROR-gamma isoform 1 | Mus musculus (house mouse) | Potency | 12.5893 | 0.0079 | 8.2332 | 1,122.0200 | AID2551 |
geminin | Homo sapiens (human) | Potency | 10.9444 | 0.0046 | 11.3741 | 33.4983 | AID624296; AID624297 |
survival motor neuron protein isoform d | Homo sapiens (human) | Potency | 3.1623 | 0.1259 | 12.2344 | 35.4813 | AID1458 |
lethal factor (plasmid) | Bacillus anthracis str. A2012 | Potency | 25.1189 | 0.0200 | 10.7869 | 31.6228 | AID912 |
lamin isoform A-delta10 | Homo sapiens (human) | Potency | 11.2202 | 0.8913 | 12.0676 | 28.1838 | AID1487 |
Glycoprotein hormones alpha chain | Homo sapiens (human) | Potency | 28.1838 | 4.4668 | 8.3448 | 10.0000 | AID624291 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Protein | Taxonomy | Measurement | Average | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
Mitogen-activated protein kinase 10 | Homo sapiens (human) | IC50 (µMol) | 62.3900 | 0.0020 | 1.7035 | 10.0000 | AID1284 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Protein | Taxonomy | Measurement | Average | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
WEE1 homolog (S. pombe) | Homo sapiens (human) | EC50 (µMol) | 7.8660 | 1.8420 | 3.8500 | 7.8660 | AID1412 |
cyclin B1 | Homo sapiens (human) | EC50 (µMol) | 49.7500 | 1.8420 | 1.8420 | 1.8420 | AID1414 |
nuclear factor NF-kappa-B p105 subunit isoform 1 | Homo sapiens (human) | EC50 (µMol) | 10.4690 | 0.0590 | 5.5596 | 27.2100 | AID1241 |
transcription factor p65 isoform 1 | Homo sapiens (human) | EC50 (µMol) | 10.4690 | 0.0590 | 5.5596 | 27.2100 | AID1241 |
Estrogen receptor beta | Mus musculus (house mouse) | EC50 (µMol) | 10.4690 | 0.0590 | 5.5596 | 27.2100 | AID1241 |
Muscarinic acetylcholine receptor M1 | Rattus norvegicus (Norway rat) | EC50 (µMol) | 49.7500 | 0.0000 | 1.2626 | 10.0000 | AID1414 |
Muscarinic acetylcholine receptor M3 | Rattus norvegicus (Norway rat) | EC50 (µMol) | 49.7500 | 0.0000 | 0.7646 | 10.0000 | AID1414 |
Muscarinic acetylcholine receptor M4 | Rattus norvegicus (Norway rat) | EC50 (µMol) | 49.7500 | 0.0000 | 0.9905 | 10.0000 | AID1414 |
Muscarinic acetylcholine receptor M5 | Rattus norvegicus (Norway rat) | EC50 (µMol) | 49.7500 | 0.0000 | 1.0528 | 10.0000 | AID1414 |
Muscarinic acetylcholine receptor M2 | Rattus norvegicus (Norway rat) | EC50 (µMol) | 49.7500 | 0.0000 | 1.1605 | 10.0000 | AID1414 |
Estrogen receptor | Mus musculus (house mouse) | EC50 (µMol) | 10.4690 | 0.0590 | 5.5596 | 27.2100 | AID1241 |
Muscarinic acetylcholine receptor | Cavia porcellus (domestic guinea pig) | EC50 (µMol) | 7.8660 | 0.0000 | 0.8939 | 7.8660 | AID1412 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Protein | Taxonomy | Measurement | Average | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
WEE1 homolog (S. pombe) | Homo sapiens (human) | CC50 | 49.7500 | 6.7590 | 6.7590 | 6.7590 | AID1413 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Process | via Protein(s) | Taxonomy |
---|---|---|
hormone activity | Glycoprotein hormones alpha chain | Homo sapiens (human) |
protein binding | Glycoprotein hormones alpha chain | Homo sapiens (human) |
follicle-stimulating hormone activity | Glycoprotein hormones alpha chain | Homo sapiens (human) |
JUN kinase activity | Mitogen-activated protein kinase 10 | Homo sapiens (human) |
MAP kinase kinase activity | Mitogen-activated protein kinase 10 | Homo sapiens (human) |
protein binding | Mitogen-activated protein kinase 10 | Homo sapiens (human) |
ATP binding | Mitogen-activated protein kinase 10 | Homo sapiens (human) |
protein serine kinase activity | Mitogen-activated protein kinase 10 | Homo sapiens (human) |
[Information is prepared from geneontology information from the June-17-2024 release] |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2006 | Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5 | Microsphere-based protease assays and screening application for lethal factor and factor Xa. |
AID588499 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1 | High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2006 | Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5 | Microsphere-based protease assays and screening application for lethal factor and factor Xa. |
AID588501 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1 | High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID504812 | Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | 2010 | Endocrinology, Jul, Volume: 151, Issue:7 | A small molecule inverse agonist for the human thyroid-stimulating hormone receptor. |
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2010 | Current protocols in cytometry, Oct, Volume: Chapter 13 | Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening. |
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2006 | Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5 | Microsphere-based protease assays and screening application for lethal factor and factor Xa. |
AID588497 | High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set | 2010 | Assay and drug development technologies, Feb, Volume: 8, Issue:1 | High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors. |
AID1745845 | Primary qHTS for Inhibitors of ATXN expression | |||
AID651635 | Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression | |||
AID504810 | Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign | 2010 | Endocrinology, Jul, Volume: 151, Issue:7 | A small molecule inverse agonist for the human thyroid-stimulating hormone receptor. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (20.00) | 29.6817 |
2010's | 3 (60.00) | 24.3611 |
2020's | 1 (20.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be weak demand-to-supply ratio for research on this compound.
| This Compound (12.56) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 5 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |