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TargetCarbonic anhydrase 2
LigandBDBM10862
Substrate/Competitorn/a
Meas. Tech.ChEMBL_588928 (CHEMBL1063843)
Ki 28900±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 Lett19:6649-54 (2009) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Carbonic anhydrase 2
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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  Blast E-value cutoff:
BDBM10862
n/a
NameBDBM10862
Synonyms:4-Amino-3-fluorobenzenesulfonamide | 4-amino-3-fluorobenzene-1-sulfonamide | CHEMBL6853 | aromatic/heteroaromatic sulfonamide 7 | halogenosulfanilamide deriv. 5b
TypeSmall organic molecule
Emp. Form.C6H7FN2O2S
Mol. Mass.190.195
SMILESNc1ccc(cc1F)S(N)(=O)=O
Structure
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