Reaction Details Report a problem with these data
Target
CARBONIC ANHYDRASE
Ligand
BDBM10891
Substrate
BDBM10856
Meas. Tech.
CA Inhibition Assay
Ki
539±n/a nM
Citation
Nishimori, I; Minakuchi, T; Morimoto, K; Sano, S; Onishi, S; Takeuchi, H; Vullo, D; Scozzafava, A; Supuran, CT Carbonic anhydrase inhibitors: DNA cloning and inhibition studies of the alpha-carbonic anhydrase from Helicobacter pylori, a new target for developing sulfonamide and sulfamate gastric drugs. J Med Chem 49:2117-26 (2006) [PubMed] Article
More Info.:
Target
Name:
CARBONIC ANHYDRASE
Synonyms:
Carbonic Anhydrase (hpCA) | hpCA
Type:
Enzyme
Mol. Mass.:
28277.52
Organism:
Helicobacter pylori J99
Description:
Q9ZK30
Residue:
247
Sequence:
MKKTFLIALALTASLIGAENTKWDYKNKENGPHRWDKLHKDFEVCKSGKSQSPINIEHYYHTQDKADLQFKYAASKPKAVFFTHHTLKASFEPTNHINYRGHDYVLDNVHFHAPMEFLINNKTRPLSAHFVHKDAKGRLLVLAIGFEEGKENPNLDPILEGIQKKQNLKEVALDAFLPKSINYYHFNGSLTAPPCTEGVAWFVIEEPLEVSAKQLAEIKKRMKNSPNQRPVQPDYNTVIIKSSAETR
Inhibitor
Name:
BDBM10891
Synonyms:
2-(4-tert-Butylphenylcarboxamido)benzenesulfonamide | 4-tert-butyl-N-(2-sulfamoylphenyl)benzamide | aromatic/heteroaromatic sulfonamide 25
Type:
Small organic molecule
Emp. Form.:
C17H20N2O3S
Mol. Mass.:
332.417
SMILES:
CC(C)(C)c1ccc(cc1)C(=O)Nc1ccccc1S(N)(=O)=O