BDBM50360266 CHEMBL1928211

SMILES: CN1CCN(CC1)Nc1nc(NCCc2ccc(Cl)cc2)nc(NCCc2ccc(Cl)cc2)n1

InChI Key: InChIKey=TUPSHHMLVFMEEO-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 = 50360266   

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))	BDBM50360266 (CHEMBL1928211) Show SMILES CN1CCN(CC1)Nc1nc(NCCc2ccc(Cl)cc2)nc(NCCc2ccc(Cl)cc2)n1 Show InChI InChI=1S/C24H30Cl2N8/c1-33-14-16-34(17-15-33)32-24-30-22(27-12-10-18-2-6-20(25)7-3-18)29-23(31-24)28-13-11-19-4-8-21(26)9-5-19/h2-9H,10-17H2,1H3,(H3,27,28,29,30,31,32)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.40E+3	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