BDBM50528114 CHEMBL4459602

SMILES: CC1(NC(=O)N(CC(=O)c2ccc(Cl)s2)C1=O)c1ccc(cc1)S(N)(=O)=O

InChI Key: InChIKey=UEVOBVXQFCZNMZ-UHFFFAOYSA-N

Data: 2 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 2 hits for monomerid = 50528114   

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
Decaprenylphosphoryl-beta-D-ribose oxidase (Mycobacterium tuberculosis (strain ATCC 25618 / H3...)	BDBM50528114 (CHEMBL4459602) Show SMILES CC1(NC(=O)N(CC(=O)c2ccc(Cl)s2)C1=O)c1ccc(cc1)S(N)(=O)=O Show InChI InChI=1S/C16H14ClN3O5S2/c1-16(9-2-4-10(5-3-9)27(18,24)25)14(22)20(15(23)19-16)8-11(21)12-6-7-13(17)26-12/h2-7H,8H2,1H3,(H,19,23)(H2,18,24,25)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	100	n/a	n/a	n/a	n/a	n/a	n/a
University of Antwerp Curated by ChEMBL					Assay Description Inhibition of Mycobacterium tuberculosis DprE1 expressed in Escherichia coli BL21(DE3) cells				J Med Chem 63: 5367-5386 (2020) Article DOI: 10.1021/acs.jmedchem.0c00107
					More data for this Ligand-Target Pair
1,3-beta-glucan synthase component GLS2 (Saccharomyces cerevisiae)	BDBM50528114 (CHEMBL4459602) Show SMILES CC1(NC(=O)N(CC(=O)c2ccc(Cl)s2)C1=O)c1ccc(cc1)S(N)(=O)=O Show InChI InChI=1S/C16H14ClN3O5S2/c1-16(9-2-4-10(5-3-9)27(18,24)25)14(22)20(15(23)19-16)8-11(21)12-6-7-13(17)26-12/h2-7H,8H2,1H3,(H,19,23)(H2,18,24,25)	KEGG UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	<5.01E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Antwerp Curated by ChEMBL					Assay Description Inhibition of human ERG expressed in CHOK1/ HEK293 cells at -80 mV holding potential by IonWorks patch-clamp assay				J Med Chem 63: 5367-5386 (2020) Article DOI: 10.1021/acs.jmedchem.0c00107
					More data for this Ligand-Target Pair