Target
Carbonic anhydrase 2
Ligand
BDBM50160673
Substrate
n/a
Meas. Tech.
ChEMBL_302349 (CHEMBL828932)
Ki
2±n/a nM
Citation
 Vullo, DVoipio, JInnocenti, ARivera, CRanki, HScozzafava, AKaila, KSupuran, CT Carbonic anhydrase inhibitors. Inhibition of the human cytosolic isozyme VII with aromatic and heterocyclic sulfonamides. Bioorg Med Chem Lett 15:971-6 (2005) [PubMed]  Article 
Target
Name:
Carbonic anhydrase 2
Synonyms:
CA-II | CA2 | CAC | CAH2_HUMAN | Carbonate dehydratase II | Carbonic anhydrase 2 (CA II) | Carbonic anhydrase 2 (CA-II) | Carbonic anhydrase 2 (Recombinant CA II) | Carbonic anhydrase C | Carbonic anhydrase II (CA II) | Carbonic anhydrase II (CA-II) | Carbonic anhydrase II (CAII) | Carbonic anhydrase II (hCA II) | Carbonic anhydrase isoenzyme II (hCA II)
Type:
Enzyme
Mol. Mass.:
29250.71
Organism:
Homo sapiens (Human)
Description:
P00918
Residue:
260
Sequence:
MSHHWGYGKHNGPEHWHKDFPIAKGERQSPVDIDTHTAKYDPSLKPLSVSYDQATSLRILNNGHAFNVEFDDSQDKAVLKGGPLDGTYRLIQFHFHWGSLDGQGSEHTVDKKKYAAELHLVHWNTKYGDFGKAVQQPDGLAVLGIFLKVGSAKPGLQKVVDVLDSIKTKGKSADFTNFDPRGLLPESLDYWTYPGSLTTPPLLECVTWIVLKEPISVSSEQVLKFRKLNFNGEGEPEELMVDNWRPAQPLKNRQIKASFK
  
Inhibitor
Name:
BDBM50160673
Synonyms:
5-(4-Amino-benzenesulfonylamino)-4,5-dihydro-[1,3,4]thiadiazole-2-sulfonic acid amide | CHEMBL427312
Type:
Small organic molecule
Emp. Form.:
C8H11N5O4S3
Mol. Mass.:
337.399
SMILES:
Nc1ccc(cc1)S(=O)(=O)NC1=NNC(S1)S(N)(=O)=O |t:12|
Structure:
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