BDBM50277636 2-(3-Benzo[d]imidazo[2,1-b]thiazol-2-yl-propionylamino)-benzoic acid::CHEMBL520620

SMILES OC(=O)c1ccccc1NC(=O)CCc1cn2c(n1)sc1ccccc21

InChI Key InChIKey=FRKCVFRGEZCWGJ-UHFFFAOYSA-N

Data  2 IC50  1 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50277636   

TargetHydroxycarboxylic acid receptor 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50277636(2-(3-Benzo[d]imidazo[2,1-b]thiazol-2-yl-propionyla...)
Affinity DataIC50: 31nMAssay Description:Displacement of [3H]niacin from human GPR109A expressed in CHO cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetHydroxycarboxylic acid receptor 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50277636(2-(3-Benzo[d]imidazo[2,1-b]thiazol-2-yl-propionyla...)
Affinity DataEC50:  690nMAssay Description:Agonist activity at human GPR109A expressed in CHOK1 cells by [35S]GTPgammaS binding assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetCytochrome P450 2C9(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50277636(2-(3-Benzo[d]imidazo[2,1-b]thiazol-2-yl-propionyla...)
Affinity DataIC50: 4.40E+3nMAssay Description:Inhibition of CYP2C9 in human liver microsomes using diclofenac substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed