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Structural Insights into Schistosoma mansoni Carbonic Anhydrase (SmCA) Inhibition by Selenoureido-Substituted Benzenesulfonamides.
- Source :
-
Journal of medicinal chemistry [J Med Chem] 2021 Jul 22; Vol. 64 (14), pp. 10418-10428. Date of Electronic Publication: 2021 Jul 07. - Publication Year :
- 2021
-
Abstract
- Tegumental carbonic anhydrase from the worm Schistosoma mansoni (SmCA) is considered a new anti-parasitic target because suppressing its expression interferes with schistosome metabolism and virulence. Here, we present the inhibition profiles of selenoureido compounds on recombinant SmCA and resolution of the first X-ray crystal structures of SmCA in adduct with a selection of such inhibitors. The key molecular features of such compounds in adduct with SmCA were obtained and compared to the human isoform hCA II, in order to understand the main structural factors responsible for enzymatic affinity and selectivity. Compounds that more specifically inhibited the schistosome versus human enzymes were identified. The results expand current knowledge in the field and pave the way for the development of more potent antiparasitic agents in the near future.
- Subjects :
- Animals
Benzene Derivatives chemical synthesis
Benzene Derivatives chemistry
Carbonic Anhydrase Inhibitors chemical synthesis
Carbonic Anhydrase Inhibitors chemistry
Crystallography, X-Ray
Dose-Response Relationship, Drug
Models, Molecular
Molecular Structure
Organoselenium Compounds chemical synthesis
Organoselenium Compounds chemistry
Structure-Activity Relationship
Sulfonamides chemical synthesis
Sulfonamides chemistry
Benzene Derivatives pharmacology
Carbonic Anhydrase Inhibitors pharmacology
Carbonic Anhydrases metabolism
Organoselenium Compounds pharmacology
Schistosoma mansoni enzymology
Sulfonamides pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1520-4804
- Volume :
- 64
- Issue :
- 14
- Database :
- MEDLINE
- Journal :
- Journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 34232641
- Full Text :
- https://doi.org/10.1021/acs.jmedchem.1c00840