Reaction Details Report a problem with these data
Target
CARBONIC ANHYDRASE
Ligand
BDBM10898
Substrate
BDBM10856
Meas. Tech.
CA Inhibition Assay
Ki
318±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:
BDBM10898
Synonyms:
1-N-(4-tert-butylbenzene)benzene-1,3-disulfonamide | 3-(4-tert-Butylphenylsulfonamido)benzenesulfonamide | aromatic/heteroaromatic sulfonamide 32
Type:
Small organic molecule
Emp. Form.:
C16H20N2O4S2
Mol. Mass.:
368.471
SMILES:
CC(C)(C)c1ccc(cc1)S(=O)(=O)Nc1cccc(c1)S(N)(=O)=O