Reaction Details Report a problem with these data
Target
CARBONIC ANHYDRASE
Ligand
BDBM10870
Substrate
BDBM10856
Meas. Tech.
CA Inhibition Assay
Ki
268±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:
BDBM10870
Synonyms:
2-N-(4-aminobenzene)-1,3,4-thiadiazole-2,5-disulfonamide | Aminobenzolamide 12 | CHEMBL268439 | aminobenzolamide 17a | aminobenzolamide deriv. 43 | aromatic/heteroaromatic sulfonamide 15
Type:
Small organic molecule
Emp. Form.:
C8H9N5O4S3
Mol. Mass.:
335.383
SMILES:
Nc1ccc(cc1)S(=O)(=O)Nc1nnc(s1)S(N)(=O)=O