Reaction Details |
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Target | Carbonic anhydrase 2 |
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Ligand | BDBM10864 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_588928 (CHEMBL1063843) |
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Ki | 31600±n/a nM |
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Citation | Carta, F; Maresca, A; Covarrubias, AS; Mowbray, SL; Jones, TA; Supuran, CT Carbonic anhydrase inhibitors. Characterization and inhibition studies of the most active beta-carbonic anhydrase from Mycobacterium tuberculosis, Rv3588c. Bioorg Med Chem Lett19:6649-54 (2009) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Carbonic anhydrase 2 |
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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: | MPNTNPVAAWKALKEGNERFVAGRPQHPSQSVDHRAGLAAGQKPTAVIFGCADSRVAAEI
IFDQGLGDMFVVRTAGHVIDSAVLGSIEYAVTVLNVPLIVVLGHDSCGAVNAALAAINDG
TLPGGYVRDVVERVAPSVLLGRRDGLSRVDEFEQRHVHETVAILMARSSAISERIAGGSL
AIVGVTYQLDDGRAVLRDHIGNIGEEV
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BDBM10864 |
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n/a |
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Name | BDBM10864 |
Synonyms: | 4-Amino-3-bromobenzenesulfonamide | 4-amino-3-bromobenzene-1-sulfonamide | CHEMBL6724 | aromatic/heteroaromatic sulfonamide 9 | halogenosulfanilamide deriv. 5d |
Type | Small organic molecule |
Emp. Form. | C6H7BrN2O2S |
Mol. Mass. | 251.101 |
SMILES | Nc1ccc(cc1Br)S(N)(=O)=O |
Structure |
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