BDBM50528100 CHEMBL4590127

SMILES: CC1(NC(=O)N(CC(=O)C2CCCCC2)C1=O)c1ccc(cc1)S(N)(=O)=O

InChI Key: InChIKey=KWISBLIGSXXQRQ-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 = 50528100   

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
1,3-beta-glucan synthase component GLS2 (Saccharomyces cerevisiae)	BDBM50528100 (CHEMBL4590127) Show SMILES CC1(NC(=O)N(CC(=O)C2CCCCC2)C1=O)c1ccc(cc1)S(N)(=O)=O Show InChI InChI=1S/C18H23N3O5S/c1-18(13-7-9-14(10-8-13)27(19,25)26)16(23)21(17(24)20-18)11-15(22)12-5-3-2-4-6-12/h7-10,12H,2-6,11H2,1H3,(H,20,24)(H2,19,25,26)	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
Decaprenylphosphoryl-beta-D-ribose oxidase (Mycobacterium tuberculosis (strain ATCC 25618 / H3...)	BDBM50528100 (CHEMBL4590127) Show SMILES CC1(NC(=O)N(CC(=O)C2CCCCC2)C1=O)c1ccc(cc1)S(N)(=O)=O Show InChI InChI=1S/C18H23N3O5S/c1-18(13-7-9-14(10-8-13)27(19,25)26)16(23)21(17(24)20-18)11-15(22)12-5-3-2-4-6-12/h7-10,12H,2-6,11H2,1H3,(H,20,24)(H2,19,25,26)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	200	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