Target
Carbonic anhydrase 2
Ligand
BDBM10863
Substrate
n/a
Meas. Tech.
ChEMBL_588928 (CHEMBL1063843)
Ki
27700±n/a nM
Citation
 Carta, FMaresca, ACovarrubias, ASMowbray, SLJones, TASupuran, CT Carbonic anhydrase inhibitors. Characterization and inhibition studies of the most active beta-carbonic anhydrase from Mycobacterium tuberculosis, Rv3588c. Bioorg Med Chem Lett 19:6649-54 (2009) [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:
BDBM10863
Synonyms:
4-Amino-3-chlorobenzenesulfonamide | 4-amino-3-chlorobenzene-1-sulfonamide | CHEMBL7092 | aromatic/heteroaromatic sulfonamide 8 | halogenosulfanilamide deriv. 5c
Type:
Small organic molecule
Emp. Form.:
C6H7ClN2O2S
Mol. Mass.:
206.65
SMILES:
Nc1ccc(cc1Cl)S(N)(=O)=O
Structure:
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