Selenolesterase enzyme activity of carbonic anhydrases.


Journal

Chemical communications (Cambridge, England)
ISSN: 1364-548X
Titre abrégé: Chem Commun (Camb)
Pays: England
ID NLM: 9610838

Informations de publication

Date de publication:
25 Apr 2020
Historique:
pubmed: 21 3 2020
medline: 29 12 2020
entrez: 21 3 2020
Statut: ppublish

Résumé

Carbonic anhydrases (CAs, E.C. 4.2.1.1) are metalloenzymes expressed on a variety of cell types. Their overexpression leads to serious pathologies, including cancer. The discovery of a series of selenolesters with high structural diversity as novel CA inhibitors is reported here. These compounds show remarkable in vitro inhibition against a panel of human CA isoforms such as hCA I, II, IX and XII. We observed that they undergo a CA mediated hydrolysis, releasing different active selenol fragments, which act as CA inhibitors. Notably, to the best of our knowledge, this is the first example of an enzyme with selenolesterase activity. In addition, X-ray crystallographic data support the proposed mechanism, proving selenolesters as novel pro-drug inhibitors with potential pharmacological applications.

Identifiants

pubmed: 32195510
doi: 10.1039/d0cc00995d
doi:

Substances chimiques

Carbonic Anhydrase Inhibitors 0
Esters 0
Isoenzymes 0
Prodrugs 0
Selenium Compounds 0
Esterases EC 3.1.-
Carbonic Anhydrase II EC 4.2.1.-
Carbonic Anhydrases EC 4.2.1.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

4444-4447

Auteurs

Andrea Angeli (A)

University of Florence, NEUROFARBA Department, Sezione di Scienze Farmaceutiche, Via Ugo Schiff 6, 50019 Sesto Fiorentino (Florence), Italy. claudiu.supuran@unifi.it.

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Classifications MeSH