BDBM50342184 CHEMBL1766185::rac-N-[4'-[Cyclopropyl(hydroxy)-1H-imidazol-4-ylmethyl][1,1'-biphenyl]-3-yl]acetamide

SMILES: CC(=O)Nc1cccc(c1)-c1ccc(cc1)C(O)(C1CC1)c1cnc[nH]1

InChI Key: InChIKey=WAXZAJPOBWYNFU-UHFFFAOYSA-N

Data: 3 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 3 hits for monomerid = 50342184   

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 17A1 (Rattus norvegicus (Rat))	BDBM50342184 (CHEMBL1766185 | rac-N-[4'-[Cyclopropyl(hydroxy)-1H...) Show SMILES CC(=O)Nc1cccc(c1)-c1ccc(cc1)C(O)(C1CC1)c1cnc[nH]1 Show InChI InChI=1S/C21H21N3O2/c1-14(25)24-19-4-2-3-16(11-19)15-5-7-17(8-6-15)21(26,18-9-10-18)20-12-22-13-23-20/h2-8,11-13,18,26H,9-10H2,1H3,(H,22,23)(H,24,25)	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	81	n/a	n/a	n/a	n/a	n/a	n/a
Takeda Pharmaceutical Company, Ltd Curated by ChEMBL					Assay Description Inhibition of 17,20 lyase activity in Sprague-Dawley rat testicular microsomes				Bioorg Med Chem 19: 2428-42 (2011) Article DOI: 10.1016/j.bmc.2011.02.009 BindingDB Entry DOI: 10.7270/Q2FJ2H3G
					More data for this Ligand-Target Pair
Cytochrome P450 3A4 (Homo sapiens (Human))	BDBM50342184 (CHEMBL1766185 | rac-N-[4'-[Cyclopropyl(hydroxy)-1H...) Show SMILES CC(=O)Nc1cccc(c1)-c1ccc(cc1)C(O)(C1CC1)c1cnc[nH]1 Show InChI InChI=1S/C21H21N3O2/c1-14(25)24-19-4-2-3-16(11-19)15-5-7-17(8-6-15)21(26,18-9-10-18)20-12-22-13-23-20/h2-8,11-13,18,26H,9-10H2,1H3,(H,22,23)(H,24,25)	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	5.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Takeda Pharmaceutical Company, Ltd Curated by ChEMBL					Assay Description Inhibition of human CYP3A4 after 30 mins				Bioorg Med Chem 19: 2428-42 (2011) Article DOI: 10.1016/j.bmc.2011.02.009 BindingDB Entry DOI: 10.7270/Q2FJ2H3G
					More data for this Ligand-Target Pair
Cytochrome P450 17A1 (Homo sapiens (Human))	BDBM50342184 (CHEMBL1766185 | rac-N-[4'-[Cyclopropyl(hydroxy)-1H...) Show SMILES CC(=O)Nc1cccc(c1)-c1ccc(cc1)C(O)(C1CC1)c1cnc[nH]1 Show InChI InChI=1S/C21H21N3O2/c1-14(25)24-19-4-2-3-16(11-19)15-5-7-17(8-6-15)21(26,18-9-10-18)20-12-22-13-23-20/h2-8,11-13,18,26H,9-10H2,1H3,(H,22,23)(H,24,25)	PDB 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	45	n/a	n/a	n/a	n/a	n/a	n/a
Takeda Pharmaceutical Company, Ltd Curated by ChEMBL					Assay Description Inhibition of human 17,20 lyase activity				Bioorg Med Chem 19: 2428-42 (2011) Article DOI: 10.1016/j.bmc.2011.02.009 BindingDB Entry DOI: 10.7270/Q2FJ2H3G
					More data for this Ligand-Target Pair