BDBM50360262 CHEMBL1928207

SMILES: CN(C)CCN1CCN(CC1)c1nc(NCCc2ccc(F)cc2)nc(NCCc2ccc(F)cc2)n1

InChI Key: InChIKey=BMAVRMFAHFSTPE-UHFFFAOYSA-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 = 50360262   

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
Vanilloid receptor (Rattus norvegicus (rat))	BDBM50360262 (CHEMBL1928207) Show SMILES CN(C)CCN1CCN(CC1)c1nc(NCCc2ccc(F)cc2)nc(NCCc2ccc(F)cc2)n1 Show InChI InChI=1S/C27H36F2N8/c1-35(2)15-16-36-17-19-37(20-18-36)27-33-25(30-13-11-21-3-7-23(28)8-4-21)32-26(34-27)31-14-12-22-5-9-24(29)10-6-22/h3-10H,11-20H2,1-2H3,(H2,30,31,32,33,34)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.86E+4	n/a	n/a	n/a	n/a	n/a	n/a
Institut de Qu£mica Avan£ada de Catalunya Curated by ChEMBL					Assay Description Antagonist activity at rat TRPV1 expressed in Xenopus laevis oocytes assessed as blockage of capsaicin-induced current at holding potential -60 mV by...				J Med Chem 54: 7441-52 (2011) Article DOI: 10.1021/jm200981s BindingDB Entry DOI: 10.7270/Q2M32W6F
					More data for this Ligand-Target Pair