null

SMILES: CC(C)N(C(C)C)C(=O)[C@H]1CCC2C3CC(C)=C4C=C(CC[C@]4(C)C3CC[C@]12C)C(O)=O

InChI Key: InChIKey=QSMQHWFDJPPRLO-SFUYFSFHSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50406346   

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
3-oxo-5-alpha-steroid 4-dehydrogenase 1/2 (Rattus norvegicus)	BDBM50406346 (CHEMBL367878) Show SMILES CC(C)N(C(C)C)C(=O)[C@H]1CCC2C3CC(C)=C4C=C(CC[C@]4(C)C3CC[C@]12C)C(O)=O |c:18,t:16| Show InChI InChI=1S/C28H43NO3/c1-16(2)29(17(3)4)25(30)23-9-8-21-20-14-18(5)24-15-19(26(31)32)10-12-28(24,7)22(20)11-13-27(21,23)6/h15-17,20-23H,8-14H2,1-7H3,(H,31,32)/t20?,21?,22?,23-,27+,28-/m1/s1	MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	200	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Smith Kline & French Laboratories Curated by ChEMBL					Assay Description In vitro inhibition of Steroid 5-alpha-reductase in rat ventral prostates.				J Med Chem 33: 943-50 (1990) BindingDB Entry DOI: 10.7270/Q25D8QSB
					More data for this Ligand-Target Pair
3-oxo-5-alpha-steroid 4-dehydrogenase 2 (Homo sapiens (Human))	BDBM50406346 (CHEMBL367878) Show SMILES CC(C)N(C(C)C)C(=O)[C@H]1CCC2C3CC(C)=C4C=C(CC[C@]4(C)C3CC[C@]12C)C(O)=O |c:18,t:16| Show InChI InChI=1S/C28H43NO3/c1-16(2)29(17(3)4)25(30)23-9-8-21-20-14-18(5)24-15-19(26(31)32)10-12-28(24,7)22(20)11-13-27(21,23)6/h15-17,20-23H,8-14H2,1-7H3,(H,31,32)/t20?,21?,22?,23-,27+,28-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	170	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Smith Kline & French Laboratories Curated by ChEMBL					Assay Description In vitro inhibition of Steroid 5-alpha-reductase in human prostatic tissue.				J Med Chem 33: 943-50 (1990) BindingDB Entry DOI: 10.7270/Q25D8QSB
					More data for this Ligand-Target Pair