Target
Carbonic anhydrase 12
Ligand
BDBM10865
Substrate
n/a
Meas. Tech.
ChEMBL_303220 (CHEMBL827186)
Ki
11±n/a nM
Citation
 Nishimori, IVullo, DInnocenti, AScozzafava, AMastrolorenzo, ASupuran, CT Carbonic anhydrase inhibitors: inhibition of the transmembrane isozyme XIV with sulfonamides. Bioorg Med Chem Lett 15:3828-33 (2005) [PubMed]  Article 
Target
Name:
Carbonic anhydrase 12
Synonyms:
CA-XII | CA12 | CAH12_HUMAN | Carbonate dehydratase XII | Carbonic anhydrase | Carbonic anhydrase 12 (CA XII) | Carbonic anhydrase XII | Carbonic anhydrase XII (CA XII) | Carbonic anhydrase XII (CAXII) | Tumor antigen HOM-RCC-3.1.3
Type:
Enzyme
Mol. Mass.:
39456.00
Organism:
Homo sapiens (Human)
Description:
Catalytic domain of human cloned isozyme was used in the assay
Residue:
354
Sequence:
MPRRSLHAAAVLLLVILKEQPSSPAPVNGSKWTYFGPDGENSWSKKYPSCGGLLQSPIDLHSDILQYDASLTPLEFQGYNLSANKQFLLTNNGHSVKLNLPSDMHIQGLQSRYSATQLHLHWGNPNDPHGSEHTVSGQHFAAELHIVHYNSDLYPDASTASNKSEGLAVLAVLIEMGSFNPSYDKIFSHLQHVKYKGQEAFVPGFNIEELLPERTAEYYRYRGSLTTPPCNPTVLWTVFRNPVQISQEQLLALETALYCTHMDDPSPREMINNFRQVQKFDERLVYTSFSQVQVCTAAGLSLGIILSLALAGILGICIVVVVSIWLFRRKSIKKGDNKGVIYKPATKMETEAHA
  
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:
Search PDB for entries with ligand similarity: