BDBM50339875 (S)-2-(3-(1-(4-(benzo[b]thiophen-2-yl)pyrimidin-2-yl)piperidin-3-yl)-2-methyl-1H-pyrrolo[2,3-b]pyridin-1-yl)ethanol::CHEMBL1761457

SMILES: Cc1c([C@@H]2CCCN(C2)c2nccc(n2)-c2cc3ccccc3s2)c2cccnc2n1CCO

InChI Key: InChIKey=RXVRDGZXPYUYJA-HXUWFJFHSA-N

Data: 4 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50339875   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Fatty-acid amide hydrolase 1 (Homo sapiens (Human))	BDBM50339875 ((S)-2-(3-(1-(4-(benzo[b]thiophen-2-yl)pyrimidin-2-...) Show SMILES Cc1c([C@@H]2CCCN(C2)c2nccc(n2)-c2cc3ccccc3s2)c2cccnc2n1CCO |r| Show InChI InChI=1S/C27H27N5OS/c1-18-25(21-8-4-11-28-26(21)32(18)14-15-33)20-7-5-13-31(17-20)27-29-12-10-22(30-27)24-16-19-6-2-3-9-23(19)34-24/h2-4,6,8-12,16,20,33H,5,7,13-15,17H2,1H3/t20-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
Amgen Inc. Curated by ChEMBL					Assay Description Inhibition of human FAAH assessed as hydrolysis of anandamidoaminomethylcumarin				Bioorg Med Chem Lett 21: 2492-6 (2011) Article DOI: 10.1016/j.bmcl.2011.02.052 BindingDB Entry DOI: 10.7270/Q2BG2P9M
					More data for this Ligand-Target Pair
Fatty-acid amide hydrolase 1 (aa 30-579) (Rattus norvegicus (rat))	BDBM50339875 ((S)-2-(3-(1-(4-(benzo[b]thiophen-2-yl)pyrimidin-2-...) Show SMILES Cc1c([C@@H]2CCCN(C2)c2nccc(n2)-c2cc3ccccc3s2)c2cccnc2n1CCO |r| Show InChI InChI=1S/C27H27N5OS/c1-18-25(21-8-4-11-28-26(21)32(18)14-15-33)20-7-5-13-31(17-20)27-29-12-10-22(30-27)24-16-19-6-2-3-9-23(19)34-24/h2-4,6,8-12,16,20,33H,5,7,13-15,17H2,1H3/t20-/m1/s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	53	n/a	n/a	n/a	n/a	n/a	n/a
Amgen Inc. Curated by ChEMBL					Assay Description Inhibition of rat FAAH assessed as hydrolysis of anandamidoaminomethylcumarin				Bioorg Med Chem Lett 21: 2492-6 (2011) Article DOI: 10.1016/j.bmcl.2011.02.052 BindingDB Entry DOI: 10.7270/Q2BG2P9M
					More data for this Ligand-Target Pair
Fatty-acid amide hydrolase 1 (aa 30-579) (Rattus norvegicus (rat))	BDBM50339875 ((S)-2-(3-(1-(4-(benzo[b]thiophen-2-yl)pyrimidin-2-...) Show SMILES Cc1c([C@@H]2CCCN(C2)c2nccc(n2)-c2cc3ccccc3s2)c2cccnc2n1CCO |r| Show InChI InChI=1S/C27H27N5OS/c1-18-25(21-8-4-11-28-26(21)32(18)14-15-33)20-7-5-13-31(17-20)27-29-12-10-22(30-27)24-16-19-6-2-3-9-23(19)34-24/h2-4,6,8-12,16,20,33H,5,7,13-15,17H2,1H3/t20-/m1/s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	39	n/a	n/a	n/a	n/a	n/a	n/a
Amgen Inc. Curated by ChEMBL					Assay Description Inhibition of rat FAAH assessed as hydrolysis of anandamidoaminomethylcumarin				Bioorg Med Chem Lett 21: 2492-6 (2011) Article DOI: 10.1016/j.bmcl.2011.02.052 BindingDB Entry DOI: 10.7270/Q2BG2P9M
					More data for this Ligand-Target Pair
Fatty-acid amide hydrolase 1 (Homo sapiens (Human))	BDBM50339875 ((S)-2-(3-(1-(4-(benzo[b]thiophen-2-yl)pyrimidin-2-...) Show SMILES Cc1c([C@@H]2CCCN(C2)c2nccc(n2)-c2cc3ccccc3s2)c2cccnc2n1CCO |r| Show InChI InChI=1S/C27H27N5OS/c1-18-25(21-8-4-11-28-26(21)32(18)14-15-33)20-7-5-13-31(17-20)27-29-12-10-22(30-27)24-16-19-6-2-3-9-23(19)34-24/h2-4,6,8-12,16,20,33H,5,7,13-15,17H2,1H3/t20-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
Amgen Inc. Curated by ChEMBL					Assay Description Inhibition of human FAAH assessed as hydrolysis of anandamidoaminomethylcumarin				Bioorg Med Chem Lett 21: 2492-6 (2011) Article DOI: 10.1016/j.bmcl.2011.02.052 BindingDB Entry DOI: 10.7270/Q2BG2P9M
					More data for this Ligand-Target Pair