BDBM50502122 CHEMBL4441658

SMILES: Cc1ccccc1N1\C(S\C(=C/c2ccc(F)cc2)C1=O)=N\NC(=O)c1cc2ccccc2oc1=O

InChI Key: InChIKey=UUUWGBCDINHYFO-XRRXZQNGSA-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 = 50502122   

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
Probable maltase-glucoamylase 2 (Homo sapiens)	BDBM50502122 (CHEMBL4441658) Show SMILES Cc1ccccc1N1\C(S\C(=C/c2ccc(F)cc2)C1=O)=N\NC(=O)c1cc2ccccc2oc1=O Show InChI InChI=1S/C27H18FN3O4S/c1-16-6-2-4-8-21(16)31-25(33)23(14-17-10-12-19(28)13-11-17)36-27(31)30-29-24(32)20-15-18-7-3-5-9-22(18)35-26(20)34/h2-15H,1H3,(H,29,32)/b23-14-,30-27-	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	90	n/a	n/a	n/a	n/a	n/a	n/a
Babasaheb Bhimrao Ambedkar University (A Central University) Curated by ChEMBL					Assay Description Inhibition of alpha-glucosidase (unknown origin) using p-nitrophenyl-alpha-d-glucopyranoside as substrate preincubated for 5 mins followed by substra...				Eur J Med Chem 176: 343-377 (2019) Article DOI: 10.1016/j.ejmech.2019.04.025
					More data for this Ligand-Target Pair