BDBM50139710 4-Nitro-3-phenyl-5-trifluoromethyl-1H-pyrazole::CHEMBL167508

SMILES: [O-][N+](=O)c1c(n[nH]c1C(F)(F)F)-c1ccccc1

InChI Key: InChIKey=FAHRYEXMSLOYOP-UHFFFAOYSA-N

Data: 1 EC50

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 = 50139710   

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
Potassium channel, inwardly rectifying, subfamily J, member 11/Sulfonylurea receptor 1 (Homo sapiens (Human))	BDBM50139710 (4-Nitro-3-phenyl-5-trifluoromethyl-1H-pyrazole | C...) Show SMILES [O-][N+](=O)c1c(n[nH]c1C(F)(F)F)-c1ccccc1 Show InChI InChI=1S/C10H6F3N3O2/c11-10(12,13)9-8(16(17)18)7(14-15-9)6-4-2-1-3-5-6/h1-5H,(H,14,15)	PDB KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	n/a	n/a	3.00E+4	n/a	n/a	n/a	n/a
GlaxoSmithKline Research & Development Curated by ChEMBL					Assay Description Maximum activation of human KATP (SUR1/Kir6.2) channel expressed in Xenopus oocytes				Bioorg Med Chem Lett 14: 813-6 (2004) BindingDB Entry DOI: 10.7270/Q29P312R
					More data for this Ligand-Target Pair