BDBM50240750 ()-N-Cyano-N'-4-pyridinyl-N''-(1,2,2-trimethylpropyl)guanidine::(+/-)-Pinacidil::4N-cyanoimino(1,2,2-trimethylpropylamino)methyl-4-pyridinamine(Pinacidil)::4N-cyanoimino[1,2,2-trimethyl-(1R)-propylamino]methyl-4-pyridinamine::4N-cyanoimino[1,2,2-trimethyl-(1S)-propylamino]methyl-4-pyridinamine::CHEMBL1159::N''-cyano-N-pyridin-4-yl-N'-(1,2,2-trimethylpropyl)guanidine::N''-cyano-N-pyridin-4-yl-N'-(1,2,2-trimethylpropyl)guanidine ((+)-pinacidil)::N''-cyano-N-pyridin-4-yl-N'-(1,2,2-trimethylpropyl)guanidine (Pinacidil)::N''-cyano-N-pyridin-4-yl-N'-[(1R)-1,2,2-trimethylpropyl]guanidine::N''-cyano-N-pyridin-4-yl-N'-[(1S)-1,2,2-trimethylpropyl]guanidine::N-Pyridin-4-yl-N'-(1,2,2-trimethyl-propyl)-cyanoguanidine (pinacidil)::PINACIDIL

SMILES CC(NC(NC#N)=Nc1ccncc1)C(C)(C)C

InChI Key InChIKey=IVVNZDGDKPTYHK-UHFFFAOYSA-N

Data  1 KI  1 EC50

  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 2 hits for monomerid = 50240750   

TargetATP-binding cassette sub-family C member 9/ATP-sensitive inward rectifier potassium channel 11(Human)
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM50240750(()-N-Cyano-N'-4-pyridinyl-N''-(1,2,2-trimethylprop...)
Affinity DataKi:  320nMAssay Description:Binding affinity was determined by displacement of [3H]-P1075 from its binding sites in canine cardiac membranesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetATP-binding cassette sub-family C member 9(Human)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandPNGBDBM50240750(()-N-Cyano-N'-4-pyridinyl-N''-(1,2,2-trimethylprop...)
Affinity DataEC50:  3.54E+3nMAssay Description:Channel opening activity at SUR2B/Kir6.2 potassium ATP channel in human TE671 cells assessed as isometric force by FLIPRMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed