BDBM8925 3-(pyridin-3-yl)quinoline::3-Pyridin-3-yl-quinoline::CHEMBL178453::Pyridine-substituted quinoline 19::US8609708, 83::cid_11701255

SMILES c1ccc2ncc(cc2c1)-c1cccnc1

InChI Key InChIKey=TYVWGQYBWPFUKK-UHFFFAOYSA-N

Data  1 KI  2 IC50  1 Other

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 8925   

TargetCytochrome P450 11B2, mitochondrial(Human)
Saarland University

LigandPNGBDBM8925(3-Pyridin-3-yl-quinoline | cid_11701255 | 3-(pyrid...)
Affinity DatapH: 7.4 T: 2°CAssay Description:The enzyme activity was assayed by monitoring the conversion of deoxycorticosterone to corticosterone in the presence of inhibitor compounds. The pro...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/1/2006
Entry Details Article
PubMed
TargetAlkaline phosphatase, tissue-nonspecific isozyme(Human)
Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM8925(3-Pyridin-3-yl-quinoline | cid_11701255 | 3-(pyrid...)
Affinity DataIC50: 1.00E+5nMAssay Description:Sanford-Burnham Center for Chemical Genomics (SBCCG) Sanford-Burnham Medical Research Institute (SBMRI, San Diego, CA) NIH Molecular Libraries Screen...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/28/2011
Entry Details
PCBioAssay
TargetCytochrome P450 2A6(Human)
Human Biomolecular Research Institute

US Patent
LigandPNGBDBM8925(3-Pyridin-3-yl-quinoline | cid_11701255 | 3-(pyrid...)
Affinity DataIC50: 2.67E+5nMAssay Description:The inhibition of human CYP2A6-mediated 7-hydroxy coumarin formation was evaluated in the presence of 95 selected test compounds in a standard assay ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/16/2014
Entry Details
Go to US Patent

TargetCytochrome P450 2A6(Human)
Human Biomolecular Research Institute

US Patent
LigandPNGBDBM8925(3-Pyridin-3-yl-quinoline | cid_11701255 | 3-(pyrid...)
Affinity DataKi:  4.45E+4nMAssay Description:Effect on coumarin 7-hydroxylation by human Cytochrome P-450 2A6More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2012
Entry Details Article
PubMed