BDBM16655 4-({[(phenylamino)nitroso]amino}methyl)benzene-1-sulfonamide::aromatic sulfonamide compound 20

SMILES: NS(=O)(=O)c1ccc(CNC(=O)Nc2ccccc2)cc1

InChI Key: InChIKey=YCVAPBGCROQSKB-UHFFFAOYSA-N

Data: 4 KI

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 4 hits for monomerid = 16655   

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 VA (Mus musculus (mouse))	BDBM16655 (4-({[(phenylamino)nitroso]amino}methyl)benzene-1-s...) Show SMILES NS(=O)(=O)c1ccc(CNC(=O)Nc2ccccc2)cc1 Show InChI InChI=1S/C14H15N3O3S/c15-21(19,20)13-8-6-11(7-9-13)10-16-14(18)17-12-4-2-1-3-5-12/h1-9H,10H2,(H2,15,19,20)(H2,16,17,18)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universita degli Studi di Firenze					Assay Description An Applied Photophysics stopped-flow instrument has been used for assaying the CA-catalyzed CO2 hydration activity. Phenol red has been used as indic...				J Med Chem 47: 1272-9 (2004) Article DOI: 10.1021/jm031057+ BindingDB Entry DOI: 10.7270/Q2MW2FDP
					More data for this Ligand-Target Pair
Carbonic anhydrase 2 (Homo sapiens (Human))	BDBM16655 (4-({[(phenylamino)nitroso]amino}methyl)benzene-1-s...) Show SMILES NS(=O)(=O)c1ccc(CNC(=O)Nc2ccccc2)cc1 Show InChI InChI=1S/C14H15N3O3S/c15-21(19,20)13-8-6-11(7-9-13)10-16-14(18)17-12-4-2-1-3-5-12/h1-9H,10H2,(H2,15,19,20)(H2,16,17,18)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	105	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universita degli Studi di Firenze					Assay Description Initial rates of 4-nitrophenyl acetate hydrolysis catalyzed by different CA isozymes were monitored spectrophotometrically at 400 nm. A molar absorpt...				J Med Chem 47: 1272-9 (2004) Article DOI: 10.1021/jm031057+ BindingDB Entry DOI: 10.7270/Q2MW2FDP
					More data for this Ligand-Target Pair
Carbonic Anhydrase IV (Bos taurus (bovine))	BDBM16655 (4-({[(phenylamino)nitroso]amino}methyl)benzene-1-s...) Show SMILES NS(=O)(=O)c1ccc(CNC(=O)Nc2ccccc2)cc1 Show InChI InChI=1S/C14H15N3O3S/c15-21(19,20)13-8-6-11(7-9-13)10-16-14(18)17-12-4-2-1-3-5-12/h1-9H,10H2,(H2,15,19,20)(H2,16,17,18)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	140	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universita degli Studi di Firenze					Assay Description Initial rates of 4-nitrophenyl acetate hydrolysis catalyzed by different CA isozymes were monitored spectrophotometrically at 400 nm. A molar absorpt...				J Med Chem 47: 1272-9 (2004) Article DOI: 10.1021/jm031057+ BindingDB Entry DOI: 10.7270/Q2MW2FDP
					More data for this Ligand-Target Pair
Carbonic anhydrase 1 (Homo sapiens (Human))	BDBM16655 (4-({[(phenylamino)nitroso]amino}methyl)benzene-1-s...) Show SMILES NS(=O)(=O)c1ccc(CNC(=O)Nc2ccccc2)cc1 Show InChI InChI=1S/C14H15N3O3S/c15-21(19,20)13-8-6-11(7-9-13)10-16-14(18)17-12-4-2-1-3-5-12/h1-9H,10H2,(H2,15,19,20)(H2,16,17,18)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase PC cid PC sid UniChem Similars	Article PubMed	800	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universita degli Studi di Firenze					Assay Description Initial rates of 4-nitrophenyl acetate hydrolysis catalyzed by different CA isozymes were monitored spectrophotometrically at 400 nm. A molar absorpt...				J Med Chem 47: 1272-9 (2004) Article DOI: 10.1021/jm031057+ BindingDB Entry DOI: 10.7270/Q2MW2FDP
					More data for this Ligand-Target Pair