BDBM50141093 CHEMBL3754321

SMILES: [H][C@@]12CC=C3C=C(CC[C@]3(C)[C@@]1([H])CC[C@]1(C)N(CC=C)C(=O)CC[C@@]21[H])c1nnn[nH]1

InChI Key: InChIKey=ORLWAHUCGZECGD-LEYYSGQMSA-N

Data: 1 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 1 hit for monomerid = 50141093   

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))	BDBM50141093 (CHEMBL3754321) Show SMILES [H][C@@]12CC=C3C=C(CC[C@]3(C)[C@@]1([H])CC[C@]1(C)N(CC=C)C(=O)CC[C@@]21[H])c1nnn[nH]1 |r,c:5,t:3| Show InChI InChI=1S/C23H31N5O/c1-4-13-28-20(29)8-7-19-17-6-5-16-14-15(21-24-26-27-25-21)9-11-22(16,2)18(17)10-12-23(19,28)3/h4-5,14,17-19H,1,6-13H2,2-3H3,(H,24,25,26,27)/t17-,18+,19+,22+,23+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	157	n/a	n/a	n/a	n/a	n/a	n/a
University Institute of Pharmaceutical Sciences Curated by ChEMBL					Assay Description Inhibition of human 5alpha-2 reductase expressed in HEK293 cells assessed as suppression of conversion of [3]androstenedione incubated for 30 mins by...				Bioorg Med Chem 24: 779-88 (2016) BindingDB Entry DOI: 10.7270/Q21G0P3C
					More data for this Ligand-Target Pair