Reaction Details |
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Target | Carbonic anhydrase 2 |
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Ligand | BDBM10873 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_588928 (CHEMBL1063843) |
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Ki | 2630±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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BDBM10873 |
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n/a |
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Name | BDBM10873 |
Synonyms: | 4-[(2-aminopyrimidin-4-yl)amino]benzene-1-sulfonamide | CHEMBL6633 | US9616064, Compound 1aa | aromatic/heteroaromatic sulfonamide 18 |
Type | Small organic molecule |
Emp. Form. | C10H11N5O2S |
Mol. Mass. | 265.292 |
SMILES | Nc1nccc(Nc2ccc(cc2)S(N)(=O)=O)n1 |
Structure |
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