Reaction Details Report a problem with these data
Target
Carbonic anhydrase
Ligand
BDBM10865
Substrate
n/a
Meas. Tech.
ChEMBL_303240 (CHEMBL827205)
Ki
280±n/a nM
Citation
 Zimmerman, S; Innocenti, A; Casini, A; Ferry, JG; Scozzafava, A; Supuran, CT Carbonic anhydrase inhibitors. Inhibition of the prokariotic beta and gamma-class enzymes from Archaea with sulfonamides. Bioorg Med Chem Lett 14:6001-6 (2004) [PubMed]  Article 
Target
Name:
Carbonic anhydrase
Synonyms:
CAH_METTT | CAM | Carbonic anhydrase | Gamma-carbonic anhydrase
Type:
Protein
Mol. Mass.:
26390.56
Organism:
Methanosarcina thermophila
Description:
P40881
Residue:
247
Sequence:
MMFNKQIFTILILSLSLALAGSGCISEGAEDNVAQEITVDEFSNIRENPVTPWNPEPSAPVIDPTAYIDPQASVIGEVTIGANVMVSPMASIRSDEGMPIFVGDRSNVQDGVVLHALETINEEGEPIEDNIVEVDGKEYAVYIGNNVSLAHQSQVHGPAAVGDDTFIGMQAFVFKSKVGNNCVLEPRSAAIGVTIPDGRYIPAGMVVTSQAEADKLPEVTDDYAYSHTNEAVVYVNVHLAEGYKETS
  
Inhibitor
Name:
BDBM10865
Synonyms:
4-Amino-3-iodobenzenesulfonamide | 4-amino-3-iodobenzene-1-sulfonamide | CHEMBL268177 | aromatic/heteroaromatic sulfonamide 10 | halogenosulfanilamide deriv. 5e
Type:
Small organic molecule
Emp. Form.:
C6H7IN2O2S
Mol. Mass.:
298.101
SMILES:
Nc1ccc(cc1I)S(N)(=O)=O
Structure:
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