Reaction Details Report a problem with these data
Target
Carbonic anhydrase
Ligand
BDBM10860
Substrate
n/a
Meas. Tech.
ChEMBL_303240 (CHEMBL827205)
Ki
350±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:
BDBM10860
Synonyms:
4-(aminomethyl)benzene-1-sulfonamide | CHEMBL419 | MAFENIDE | aromatic sulfonamide compound 6 | aromatic/heteroaromatic sulfonamide 5 | hCA inhibitor, 9
Type:
Small organic molecule
Emp. Form.:
C7H10N2O2S
Mol. Mass.:
186.232
SMILES:
NCc1ccc(cc1)S(N)(=O)=O
Structure:
Search PDB for entries with ligand similarity: