BDBM50325631 (1H-indol-5-yl)(2-propylpyrrolidin-2-yl)methanone::CHEMBL1224164

SMILES: CCCC1(CCCN1)C(=O)c1ccc2[nH]ccc2c1

InChI Key: InChIKey=PMWJXJVDUJHXHT-UHFFFAOYSA-N

Data: 2 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 2 hits for monomerid = 50325631   

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 2D6 (Homo sapiens (Human))	BDBM50325631 ((1H-indol-5-yl)(2-propylpyrrolidin-2-yl)methanone ...) Show SMILES CCCC1(CCCN1)C(=O)c1ccc2[nH]ccc2c1 Show InChI InChI=1S/C16H20N2O/c1-2-7-16(8-3-9-18-16)15(19)13-4-5-14-12(11-13)6-10-17-14/h4-6,10-11,17-18H,2-3,7-9H2,1H3	PDB UniProtKB/SwissProt UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	300	n/a	n/a	n/a	n/a	n/a	n/a
Roche Palo Alto LLC Curated by ChEMBL					Assay Description Inhibition of CYP2D6				Bioorg Med Chem Lett 20: 5559-66 (2010) Article DOI: 10.1016/j.bmcl.2010.07.020 BindingDB Entry DOI: 10.7270/Q20865HF
					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50325631 ((1H-indol-5-yl)(2-propylpyrrolidin-2-yl)methanone ...) Show SMILES CCCC1(CCCN1)C(=O)c1ccc2[nH]ccc2c1 Show InChI InChI=1S/C16H20N2O/c1-2-7-16(8-3-9-18-16)15(19)13-4-5-14-12(11-13)6-10-17-14/h4-6,10-11,17-18H,2-3,7-9H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Roche Palo Alto LLC Curated by ChEMBL					Assay Description Inhibition of human ERG				Bioorg Med Chem Lett 20: 5559-66 (2010) Article DOI: 10.1016/j.bmcl.2010.07.020 BindingDB Entry DOI: 10.7270/Q20865HF
					More data for this Ligand-Target Pair