BDBM50400162 CHEMBL2179440

SMILES: CC(C)(O)CNc1ncc(C(=O)N[C@H]2C3CC4CC2C[C@](O)(C4)C3)c(n1)C1CCCC1

InChI Key: InChIKey=GHKHMRLGFSCWHI-XKRYALBDSA-N

Data: 2 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 2 hits for monomerid = 50400162   

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
11-beta-hydroxysteroid dehydrogenase 1 (Homo sapiens (Human))	BDBM50400162 (CHEMBL2179440) Show SMILES CC(C)(O)CNc1ncc(C(=O)N[C@H]2C3CC4CC2C[C@](O)(C4)C3)c(n1)C1CCCC1 |r,wU:13.12,wD:20.21,TLB:21:20:13:17.16.15,12:13:23.19.20:17.16.15,12:13:15:23.20.22,THB:21:20:13.18.17:15,22:20:13:17.16.15,22:16:13:23.19.20,19:18:15:23.20.22,19:20:13.18.17:15,(40.79,-40.02,;41.57,-38.69,;42.33,-40.02,;40.24,-37.92,;42.91,-37.92,;44.24,-38.69,;45.57,-37.92,;45.57,-36.38,;46.9,-35.61,;48.24,-36.37,;49.57,-35.59,;49.56,-34.05,;50.91,-36.36,;52.24,-35.58,;52.23,-33.84,;51.2,-32.76,;51.85,-31.49,;51.87,-32.93,;53.04,-34.26,;54.45,-33.69,;54.31,-32.07,;55.84,-32.08,;53.26,-30.95,;53.53,-33.28,;48.24,-37.92,;46.91,-38.69,;49.58,-38.69,;49.74,-40.21,;51.25,-40.53,;52.02,-39.2,;50.99,-38.05,)| Show InChI InChI=1S/C24H36N4O3/c1-23(2,30)13-26-22-25-12-18(20(28-22)15-5-3-4-6-15)21(29)27-19-16-7-14-8-17(19)11-24(31,9-14)10-16/h12,14-17,19,30-31H,3-11,13H2,1-2H3,(H,27,29)(H,25,26,28)/t14?,16?,17?,19-,24-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	19	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of human 11beta-HSD1 by HTRF assay				J Med Chem 55: 10652-61 (2012) Article DOI: 10.1021/jm3013163 BindingDB Entry DOI: 10.7270/Q2BG2Q4S
					More data for this Ligand-Target Pair
11-beta-hydroxysteroid dehydrogenase 1 (Mus musculus (mouse))	BDBM50400162 (CHEMBL2179440) Show SMILES CC(C)(O)CNc1ncc(C(=O)N[C@H]2C3CC4CC2C[C@](O)(C4)C3)c(n1)C1CCCC1 |r,wU:13.12,wD:20.21,TLB:21:20:13:17.16.15,12:13:23.19.20:17.16.15,12:13:15:23.20.22,THB:21:20:13.18.17:15,22:20:13:17.16.15,22:16:13:23.19.20,19:18:15:23.20.22,19:20:13.18.17:15,(40.79,-40.02,;41.57,-38.69,;42.33,-40.02,;40.24,-37.92,;42.91,-37.92,;44.24,-38.69,;45.57,-37.92,;45.57,-36.38,;46.9,-35.61,;48.24,-36.37,;49.57,-35.59,;49.56,-34.05,;50.91,-36.36,;52.24,-35.58,;52.23,-33.84,;51.2,-32.76,;51.85,-31.49,;51.87,-32.93,;53.04,-34.26,;54.45,-33.69,;54.31,-32.07,;55.84,-32.08,;53.26,-30.95,;53.53,-33.28,;48.24,-37.92,;46.91,-38.69,;49.58,-38.69,;49.74,-40.21,;51.25,-40.53,;52.02,-39.2,;50.99,-38.05,)| Show InChI InChI=1S/C24H36N4O3/c1-23(2,30)13-26-22-25-12-18(20(28-22)15-5-3-4-6-15)21(29)27-19-16-7-14-8-17(19)11-24(31,9-14)10-16/h12,14-17,19,30-31H,3-11,13H2,1-2H3,(H,27,29)(H,25,26,28)/t14?,16?,17?,19-,24-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	48	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of mouse 11beta-HSD1 by HTRF assay				J Med Chem 55: 10652-61 (2012) Article DOI: 10.1021/jm3013163 BindingDB Entry DOI: 10.7270/Q2BG2Q4S
					More data for this Ligand-Target Pair