Target
Carbonic anhydrase 2
Ligand
BDBM10886
Substrate
n/a
Meas. Tech.
ChEMBL_588928 (CHEMBL1063843)
Ki
467±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:
BDBM10886
Synonyms:
2-N-benzene-1,3,4-thiadiazole-2,5-disulfonamide | BZA1 | Benzolamide | Benzolamide (BZA) | CHEMBL73962
Type:
Small organic molecule
Emp. Form.:
C8H8N4O4S3
Mol. Mass.:
320.369
SMILES:
NS(=O)(=O)c1nnc(NS(=O)(=O)c2ccccc2)s1
Structure:
Search PDB for entries with ligand similarity: