ID Source | ID |
---|---|
PubMed CID | 11910 |
CHEMBL ID | 1702610 |
CHEBI ID | 48984 |
SCHEMBL ID | 256942 |
MeSH ID | M0161078 |
Synonym |
---|
AC-5093 |
EN300-25427 |
8-methyl-quinoline |
o-toluquinoline |
ccris 408 |
inchi=1/c10h9n/c1-8-4-2-5-9-6-3-7-11-10(8)9/h2-7h,1h |
quinoline, 8-methyl- |
nsc9409 |
nsc-9409 |
611-32-5 |
8-methylquinoline , |
NCGC00091614-01 |
CHEBI:48984 , |
einecs 210-264-0 |
ai3-00849 |
brn 0111340 |
8-methylquinoline, 97% |
nistc611325 |
quinoline, 8-methyl- (8ci,9ci) |
ai3-0111340 |
nsc 9409 |
MLS002303012 |
smr001307318 |
FT-0660641 |
M0419 |
AKOS001287315 |
NCGC00091614-02 |
HMS3039E09 |
cas-611-32-5 |
tox21_200341 |
dtxcid80888 |
NCGC00257895-01 |
dtxsid8020888 , |
5-20-07-00405 (beilstein handbook reference) |
unii-k97b12j636 |
k97b12j636 , |
FT-0602149 |
AC-907/25014270 |
AM1097 |
SCHEMBL256942 |
8-methyl quinoline |
8-metyl quinoline |
W-204381 |
CHEMBL1702610 , |
TS-01865 |
1199266-77-7 |
methylquinoline, 8- |
J-519467 |
mfcd00006810 |
Q27121420 |
quinoline, 8-methyl- pound>>8-methyl-quinoline pound>>o-toluquinoline |
BCP27326 |
STL190850 |
bdbm50264545 |
I11487 |
quinoline, 8-methyl-, labeled with deuterium |
Z204013194 |
Class | Description |
---|---|
methylquinoline | Any member of the class of quinolines carrying at least one methyl substituent. |
[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) |
---|---|---|---|---|---|---|---|
RAR-related orphan receptor gamma | Mus musculus (house mouse) | Potency | 6.8102 | 0.0060 | 38.0041 | 19,952.5996 | AID1159521 |
ATAD5 protein, partial | Homo sapiens (human) | Potency | 11.5774 | 0.0041 | 10.8903 | 31.5287 | AID504467 |
TDP1 protein | Homo sapiens (human) | Potency | 3.2643 | 0.0008 | 11.3822 | 44.6684 | AID686978 |
AR protein | Homo sapiens (human) | Potency | 68.1016 | 0.0002 | 21.2231 | 8,912.5098 | AID743042 |
glucocorticoid receptor [Homo sapiens] | Homo sapiens (human) | Potency | 61.2152 | 0.0002 | 14.3764 | 60.0339 | AID720692 |
retinoic acid nuclear receptor alpha variant 1 | Homo sapiens (human) | Potency | 60.6957 | 0.0030 | 41.6115 | 22,387.1992 | AID1159552 |
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 | 0.0820 | 0.0041 | 9.9848 | 25.9290 | AID504444 |
nuclear factor erythroid 2-related factor 2 isoform 1 | Homo sapiens (human) | Potency | 66.8242 | 0.0006 | 27.2152 | 1,122.0200 | AID651741 |
geminin | Homo sapiens (human) | Potency | 14.6494 | 0.0046 | 11.3741 | 33.4983 | AID624296; AID624297 |
[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) |
---|---|---|---|---|---|---|---|
26S proteasome non-ATPase regulatory subunit 14 | Homo sapiens (human) | IC50 (µMol) | 100.0000 | 0.0070 | 1.0981 | 2.5000 | AID1480589 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Process | via Protein(s) | Taxonomy |
---|---|---|
protein binding | 26S proteasome non-ATPase regulatory subunit 14 | Homo sapiens (human) |
metallopeptidase activity | 26S proteasome non-ATPase regulatory subunit 14 | Homo sapiens (human) |
metal ion binding | 26S proteasome non-ATPase regulatory subunit 14 | Homo sapiens (human) |
endopeptidase activator activity | 26S proteasome non-ATPase regulatory subunit 14 | Homo sapiens (human) |
K63-linked deubiquitinase activity | 26S proteasome non-ATPase regulatory subunit 14 | Homo sapiens (human) |
proteasome binding | 26S proteasome non-ATPase regulatory subunit 14 | Homo sapiens (human) |
metal-dependent deubiquitinase activity | 26S proteasome non-ATPase regulatory subunit 14 | Homo sapiens (human) |
[Information is prepared from geneontology information from the June-17-2024 release] |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
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. |
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. |
AID1745845 | Primary qHTS for Inhibitors of ATXN expression | |||
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. |
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. |
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. |
AID651635 | Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression | |||
AID1480590 | Antiproliferative activity against human HCT116 cells after 72 hrs by Cell Titer-Glo assay | 2017 | Journal of medicinal chemistry, 02-23, Volume: 60, Issue:4 | Discovery of an Inhibitor of the Proteasome Subunit Rpn11. |
AID1480589 | Inhibition of 26S proteasome regulatory subunit RPN11 deubiquitinating activity in human erythrocytes using Ub4-pepOG protein substrate preincubated for 1 hr followed by substrate addition measured after 80 mins by fluorescence polarization assay | 2017 | Journal of medicinal chemistry, 02-23, Volume: 60, Issue:4 | Discovery of an Inhibitor of the Proteasome Subunit Rpn11. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 1 (7.69) | 18.7374 |
1990's | 1 (7.69) | 18.2507 |
2000's | 3 (23.08) | 29.6817 |
2010's | 6 (46.15) | 24.3611 |
2020's | 2 (15.38) | 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 moderate demand-to-supply ratio for research on this compound.
| This Compound (31.78) 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 | 14 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |