null

SMILES: Cc1cc(OC[P@@]2(=O)OCC[C@H](O2)c2ccc(Cl)cc2)c-2c(Cc3scnc-23)c1C

InChI Key: InChIKey=VCTMBHZQYKYSTO-RBSBEOHCSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50317153   

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
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50317153 (4-[4-(4-Chloro-phenyl)-2-oxo-2lambda*5*-[1,3,2]dio...) Show SMILES Cc1cc(OC[P@@]2(=O)OCC[C@H](O2)c2ccc(Cl)cc2)c-2c(Cc3scnc-23)c1C |r| Show InChI InChI=1S/C22H21ClNO4PS/c1-13-9-19(21-17(14(13)2)10-20-22(21)24-11-30-20)26-12-29(25)27-8-7-18(28-29)15-3-5-16(23)6-4-15/h3-6,9,11,18H,7-8,10,12H2,1-2H3/t18-,29+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	730	n/a	n/a	n/a	n/a	n/a	n/a
Daiichi Sankyo Co., Ltd Curated by ChEMBL					Assay Description Inhibition of CYP3A4				Bioorg Med Chem Lett 20: 2938-41 (2010) Article DOI: 10.1016/j.bmcl.2010.03.017 BindingDB Entry DOI: 10.7270/Q2222TXQ
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50317153 (4-[4-(4-Chloro-phenyl)-2-oxo-2lambda*5*-[1,3,2]dio...) Show SMILES Cc1cc(OC[P@@]2(=O)OCC[C@H](O2)c2ccc(Cl)cc2)c-2c(Cc3scnc-23)c1C |r| Show InChI InChI=1S/C22H21ClNO4PS/c1-13-9-19(21-17(14(13)2)10-20-22(21)24-11-30-20)26-12-29(25)27-8-7-18(28-29)15-3-5-16(23)6-4-15/h3-6,9,11,18H,7-8,10,12H2,1-2H3/t18-,29+/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	650	n/a	n/a	n/a	n/a	n/a	n/a
Daiichi Sankyo Co., Ltd Curated by ChEMBL					Assay Description Inhibition of CYP3A4				Bioorg Med Chem Lett 20: 2938-41 (2010) Article DOI: 10.1016/j.bmcl.2010.03.017 BindingDB Entry DOI: 10.7270/Q2222TXQ
					More data for this Ligand-Target Pair