BDBM50278967 CHEMBL4162981

SMILES: Oc1cc(NS(=O)(=O)c2ccc(cc2)-c2ccccc2)ccc1\C=N\NC=O

InChI Key: InChIKey=QCCKVUPLCSIIHD-FYJGNVAPSA-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 = 50278967   

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
Histone deacetylase (Homo sapiens (Human))	BDBM50278967 (CHEMBL4162981) Show SMILES Oc1cc(NS(=O)(=O)c2ccc(cc2)-c2ccccc2)ccc1\C=N\NC=O Show InChI InChI=1S/C20H17N3O4S/c24-14-22-21-13-17-6-9-18(12-20(17)25)23-28(26,27)19-10-7-16(8-11-19)15-4-2-1-3-5-15/h1-14,23,25H,(H,22,24)/b21-13+	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet	KEGG PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.92E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Catania Curated by ChEMBL					Assay Description Antagonist activity for rat histamine H3 receptor was determined				Eur J Med Chem 141: 188-196 (2017) Article DOI: 10.1016/j.ejmech.2017.09.075 BindingDB Entry DOI: 10.7270/Q2QZ2DGS
					More data for this Ligand-Target Pair