null

SMILES: NS(=O)(=O)Nc1ccc(NC(=O)NC2CCCCC2)cc1

InChI Key: InChIKey=WRANOMIXFVCXLB-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50428615   

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
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM50428615 (CHEMBL2331759) Show SMILES NS(=O)(=O)Nc1ccc(NC(=O)NC2CCCCC2)cc1 Show InChI InChI=1S/C13H20N4O3S/c14-21(19,20)17-12-8-6-11(7-9-12)16-13(18)15-10-4-2-1-3-5-10/h6-10,17H,1-5H2,(H2,14,19,20)(H2,15,16,18)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	1	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Romanian Academy Curated by ChEMBL					Assay Description Inhibition of human carbonic anhydrase-1				Bioorg Med Chem 21: 1404-9 (2013) Article DOI: 10.1016/j.bmc.2012.11.004 BindingDB Entry DOI: 10.7270/Q2XW4M4Q
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM50428615 (CHEMBL2331759) Show SMILES NS(=O)(=O)Nc1ccc(NC(=O)NC2CCCCC2)cc1 Show InChI InChI=1S/C13H20N4O3S/c14-21(19,20)17-12-8-6-11(7-9-12)16-13(18)15-10-4-2-1-3-5-10/h6-10,17H,1-5H2,(H2,14,19,20)(H2,15,16,18)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	2.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Romanian Academy Curated by ChEMBL					Assay Description Inhibition of human carbonic anhydrase-2				Bioorg Med Chem 21: 1404-9 (2013) Article DOI: 10.1016/j.bmc.2012.11.004 BindingDB Entry DOI: 10.7270/Q2XW4M4Q
					More data for this Ligand-Target Pair
Carbonic anhydrase 9 (Homo sapiens (Human))	BDBM50428615 (CHEMBL2331759) Show SMILES NS(=O)(=O)Nc1ccc(NC(=O)NC2CCCCC2)cc1 Show InChI InChI=1S/C13H20N4O3S/c14-21(19,20)17-12-8-6-11(7-9-12)16-13(18)15-10-4-2-1-3-5-10/h6-10,17H,1-5H2,(H2,14,19,20)(H2,15,16,18)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	2.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Romanian Academy Curated by ChEMBL					Assay Description Inhibition of human carbonic anhydrase-9				Bioorg Med Chem 21: 1404-9 (2013) Article DOI: 10.1016/j.bmc.2012.11.004 BindingDB Entry DOI: 10.7270/Q2XW4M4Q
					More data for this Ligand-Target Pair
Carbonic anhydrase 12 (Homo sapiens (Human))	BDBM50428615 (CHEMBL2331759) Show SMILES NS(=O)(=O)Nc1ccc(NC(=O)NC2CCCCC2)cc1 Show InChI InChI=1S/C13H20N4O3S/c14-21(19,20)17-12-8-6-11(7-9-12)16-13(18)15-10-4-2-1-3-5-10/h6-10,17H,1-5H2,(H2,14,19,20)(H2,15,16,18)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	2.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Romanian Academy Curated by ChEMBL					Assay Description Inhibition of human carbonic anhydrase-12				Bioorg Med Chem 21: 1404-9 (2013) Article DOI: 10.1016/j.bmc.2012.11.004 BindingDB Entry DOI: 10.7270/Q2XW4M4Q
					More data for this Ligand-Target Pair
Carbonic anhydrase (Candida albicans (Yeast))	BDBM50428615 (CHEMBL2331759) Show SMILES NS(=O)(=O)Nc1ccc(NC(=O)NC2CCCCC2)cc1 Show InChI InChI=1S/C13H20N4O3S/c14-21(19,20)17-12-8-6-11(7-9-12)16-13(18)15-10-4-2-1-3-5-10/h6-10,17H,1-5H2,(H2,14,19,20)(H2,15,16,18)	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	134	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universit£ degli Studi di Firenze Curated by ChEMBL					Assay Description Inhibition of recombinant full length Candida albicans NCE103 expressed in Escherichia coli BL21 preincubated for 15 mins by stopped-flow CO2 hydrase...				Bioorg Med Chem Lett 23: 2647-52 (2013) Article DOI: 10.1016/j.bmcl.2013.02.092 BindingDB Entry DOI: 10.7270/Q28S4R9P
					More data for this Ligand-Target Pair