BDBM50357545 CHEMBL1915176

SMILES: CC(C)CN1Cc2[nH]c3ccccc3c2C[C@H]1C(O)=O

InChI Key: InChIKey=CODVNZWRCKMGAX-HNNXBMFYSA-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 = 50357545   

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 19A1 (Homo sapiens (Human))	BDBM50357545 (CHEMBL1915176) Show SMILES CC(C)CN1Cc2[nH]c3ccccc3c2C[C@H]1C(O)=O |r| Show InChI InChI=1S/C16H20N2O2/c1-10(2)8-18-9-14-12(7-15(18)16(19)20)11-5-3-4-6-13(11)17-14/h3-6,10,15,17H,7-9H2,1-2H3,(H,19,20)/t15-/m0/s1	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	7.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Hawai'i at Hilo Curated by ChEMBL					Assay Description Inhibition of aromatase after 10 mins preincubation by plate reader relative to control				Bioorg Med Chem 19: 6182-95 (2011) Article DOI: 10.1016/j.bmc.2011.09.020 BindingDB Entry DOI: 10.7270/Q2Z89CTS
					More data for this Ligand-Target Pair