BDBM50271896 6-Methyl-7-[3-(piperidin-1-yl)-propoxy]-4-(6-methylbenzothiazol-2-ylamino)-quinoline-3-carbonitrile::6-methyl-4-(6-methylbenzo[d]thiazol-2-ylamino)-7-(3-(piperidin-1-yl)propoxy)quinoline-3-carbonitrile::CHEMBL526547

SMILES Cc1ccc2nc(Nc3c(cnc4cc(OCCCN5CCCCC5)c(C)cc34)C#N)sc2c1

InChI Key InChIKey=QSKOLVKPDLINDM-UHFFFAOYSA-N

Data  4 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50271896   

TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50271896(6-Methyl-7-[3-(piperidin-1-yl)-propoxy]-4-(6-methy...)
Affinity DataIC50:  15.4nMAssay Description:Inhibition of cSrc (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Mus musculus (mouse))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50271896(6-Methyl-7-[3-(piperidin-1-yl)-propoxy]-4-(6-methy...)
Affinity DataIC50:  3.13E+5nMAssay Description:Inhibition of inducible nitric oxide synthetase in LPS-stimulated mouse ANA1 macrophagesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50271896(6-Methyl-7-[3-(piperidin-1-yl)-propoxy]-4-(6-methy...)
Affinity DataIC50:  15.4nMAssay Description:Inhibition of human recombinant cSrc by ELISAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Mus musculus (mouse))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50271896(6-Methyl-7-[3-(piperidin-1-yl)-propoxy]-4-(6-methy...)
Affinity DataIC50:  3.13E+5nMAssay Description:Inhibition of iNOS in mouse ANA1 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed