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TargetCarbonic anhydrase 2
LigandBDBM13063
Substrate/Competitorn/a
Meas. Tech.ChEMBL_878776 (CHEMBL2183716)
Ki 682±n/a nM
Citation Marini, AMMaresca, AAggarwal, MOrlandini, ENencetti, SDa Settimo, FSalerno, SSimorini, FLa Motta, CTaliani, SNuti, EScozzafava, AMcKenna, RRossello, ASupuran, CT Tricyclic sulfonamides incorporating benzothiopyrano[4,3-c]pyrazole and pyridothiopyrano[4,3-c]pyrazole effectively inhibita- andß-carbonic anhydrase: X-ray crystallography and solution investigations on 15 isoforms. J Med Chem55:9619-29 (2012) [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
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM13063
n/a
NameBDBM13063
Synonyms:4-(5-methyl-3-phenyl-1,2-oxazol-4-yl)benzene-1-sulfonamide | Bextra | CHEMBL865 | VLX | Valdecoxib | cid_119607
TypeSmall organic molecule
Emp. Form.C16H14N2O3S
Mol. Mass.314.359
SMILESCc1onc(c1-c1ccc(cc1)S(N)(=O)=O)-c1ccccc1
Structure
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