BDBM50433293 CHEMBL2376323

SMILES: CCC1(C)NC(=O)c2cc(ccc2NC1=O)S(=O)(=O)NCc1ccccc1

InChI Key: InChIKey=QQMKUNLVYFAXPW-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 = 50433293   

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
Alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase (Homo sapiens (Human))	BDBM50433293 (CHEMBL2376323) Show SMILES CCC1(C)NC(=O)c2cc(ccc2NC1=O)S(=O)(=O)NCc1ccccc1 Show InChI InChI=1S/C19H21N3O4S/c1-3-19(2)18(24)21-16-10-9-14(11-15(16)17(23)22-19)27(25,26)20-12-13-7-5-4-6-8-13/h4-11,20H,3,12H2,1-2H3,(H,21,24)(H,22,23)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.94E+3	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of human recombinant MGAT2 expressed in insect cell membrane using 2-oleoyl-sn-glycerol and oleoyl coenzyme A as substrate after 40 mins b...				Bioorg Med Chem Lett 23: 2721-6 (2013) Article DOI: 10.1016/j.bmcl.2013.02.084 BindingDB Entry DOI: 10.7270/Q2GB25DM
					More data for this Ligand-Target Pair