Target
Carbonic anhydrase 2
Ligand
BDBM11607
Substrate
n/a
Meas. Tech.
CA Inhibition Assay
pH
8.3±0
Temperature
298.15±0 K
Ki
4.49e+3±n/a nM
Citation
 Maresca, AScozzafava, AVullo, DSupuran, CT Dihalogenated sulfanilamides and benzolamides are effective inhibitors of the three ß-class carbonic anhydrases from Mycobacterium tuberculosis. J Enzyme Inhib Med Chem 28:384-7 (2013) [PubMed]  Article 
Target
Name:
Carbonic anhydrase 2
Synonyms:
β-Carbonic anhydrase 2 (CA 2) | Carbonic anhydrase | MTCA2_MYCTU | canB | cynT | mtcA2
Type:
Enzyme
Mol. Mass.:
21788.97
Organism:
Mycobacterium tuberculosis
Description:
P9WPJ9
Residue:
207
Sequence:
MPNTNPVAAWKALKEGNERFVAGRPQHPSQSVDHRAGLAAGQKPTAVIFGCADSRVAAEIIFDQGLGDMFVVRTAGHVIDSAVLGSIEYAVTVLNVPLIVVLGHDSCGAVNAALAAINDGTLPGGYVRDVVERVAPSVLLGRRDGLSRVDEFEQRHVHETVAILMARSSAISERIAGGSLAIVGVTYQLDDGRAVLRDHIGNIGEEV
  
Inhibitor
Name:
BDBM11607
Synonyms:
β-CA inhibitor, 6 | 4-Amino-3-fluoro-5-iodobenzenesulfonamide | 4-amino-3-fluoro-5-iodobenzene-1-sulfonamide | CHEMBL69813 | halogenosulfanilamide deriv. 8
Type:
Small organic molecule
Emp. Form.:
C6H6FIN2O2S
Mol. Mass.:
316.092
SMILES:
Nc1c(F)cc(cc1I)S(N)(=O)=O
Structure:
Search PDB for entries with ligand similarity: