Target
Carbonic anhydrase 5A, mitochondrial
Ligand
BDBM10858
Substrate
n/a
Meas. Tech.
ChEMBL_305668 (CHEMBL827937)
IC50
7700±n/a nM
Citation
 Innocenti, AAntel, JWurl, MScozzafava, ASupuran, CT Carbonic anhydrase inhibitors: inhibition of human cytosolic isozyme II and mitochondrial isozyme V with a series of benzene sulfonamide derivatives. Bioorg Med Chem Lett 14:5703-7 (2004) [PubMed]  Article 
Target
Name:
Carbonic anhydrase 5A, mitochondrial
Synonyms:
CA-VA | CA5 | CA5A | CAH5A_HUMAN | Carbonate dehydratase VA | Carbonic Anhydrase VA | Carbonic anhydrase 5A (CA VA) | Carbonic anhydrase 5A, mitochondrial | Carbonic anhydrase 5A, mitochondrial precursor | Carbonic anhydrase V | Carbonic anhydrase VA (CA VA)
Type:
Enzyme
Mol. Mass.:
34755.54
Organism:
Homo sapiens (Human)
Description:
Human (cloned) isozyme
Residue:
305
Sequence:
MLGRNTWKTSAFSFLVEQMWAPLWSRSMRPGRWCSQRSCAWQTSNNTLHPLWTVPVSVPGGTRQSPINIQWRDSVYDPQLKPLRVSYEAASCLYIWNTGYLFQVEFDDATEASGISGGPLENHYRLKQFHFHWGAVNEGGSEHTVDGHAYPAELHLVHWNSVKYQNYKEAVVGENGLAVIGVFLKLGAHHQTLQRLVDILPEIKHKDARAAMRPFDPSTLLPTCWDYWTYAGSLTTPPLTESVTWIIQKEPVEVAPSQLSAFRTLLFSALGEEEKMMVNNYRPLQPLMNRKVWASFQATNEGTRS
  
Inhibitor
Name:
BDBM10858
Synonyms:
4-hydrazinylbenzene-1-sulfonamide | CHEMBL7204 | aromatic/heteroaromatic sulfonamide 3 | hydrazide deriv. 14
Type:
Small organic molecule
Emp. Form.:
C6H9N3O2S
Mol. Mass.:
187.22
SMILES:
NNc1ccc(cc1)S(N)(=O)=O
Structure:
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