BDBM50403608 CHEMBL439804

SMILES: C[C@]12CCC(CC1=CCc1cc(Cl)ccc21)P(=O)=O

InChI Key: InChIKey=IGXYKZRXYLEVKJ-WUJWULDRSA-N

Data: 2 KI

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 = 50403608   

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
Steroid 5-alpha-reductase (Homo sapiens (Human))	BDBM50403608 (CHEMBL439804) Show SMILES C[C@]12CCC(CC1=CCc1cc(Cl)ccc21)P(=O)=O |c:7| Show InChI InChI=1S/C15H16ClO2P/c1-15-7-6-13(19(17)18)9-11(15)3-2-10-8-12(16)4-5-14(10)15/h3-5,8,13H,2,6-7,9H2,1H3/t13?,15-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	1.60E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of type-2 human steroid 5-alpha-reductase.				Bioorg Med Chem Lett 6: 481-484 (1996) Article DOI: 10.1016/0960-894X(96)00054-6 BindingDB Entry DOI: 10.7270/Q2BZ661K
					More data for this Ligand-Target Pair
5α-Reductase 1 (5α-R1) (Homo sapiens (Human))	BDBM50403608 (CHEMBL439804) Show SMILES C[C@]12CCC(CC1=CCc1cc(Cl)ccc21)P(=O)=O |c:7| Show InChI InChI=1S/C15H16ClO2P/c1-15-7-6-13(19(17)18)9-11(15)3-2-10-8-12(16)4-5-14(10)15/h3-5,8,13H,2,6-7,9H2,1H3/t13?,15-/m0/s1	UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	1.90E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Inhibition of type-1 human steroid 5-alpha-reductase				Bioorg Med Chem Lett 6: 481-484 (1996) Article DOI: 10.1016/0960-894X(96)00054-6 BindingDB Entry DOI: 10.7270/Q2BZ661K
					More data for this Ligand-Target Pair