Inhibition of carbonic anhydrases by a substrate analog: benzyl carbamate directly coordinates the catalytic zinc ion mimicking bicarbonate binding

Author:

De Simone Giuseppina123ORCID,Angeli Andrea45678ORCID,Bozdag Murat45678ORCID,Supuran Claudiu T.45678ORCID,Winum Jean-Yves910111213ORCID,Monti Simona Maria123ORCID,Alterio Vincenzo123ORCID

Affiliation:

1. Istituto di Biostrutture e Bioimmagini-CNR

2. Naples

3. Italy

4. Neurofarba Department

5. Section of Pharmaceutical and Nutriceutical Sciences

6. Università degli Studi di Firenze

7. Sesto Fiorentino

8. Florence

9. Institut des Biomolécules Max Mousseron (IBMM) UMR 5247 CNRS

10. ENSCM

11. Université de Montpellier

12. 240 avenue du professeur Emile Jeanbrau

13. 34296 Montpellier Cedex

Abstract

N-Unsubstituted carbamates can be used as lead compounds for the development of carbonic anhydrase inhibitors possessing a binding mode similar to bicarbonate.

Funder

Consiglio Nazionale delle Ricerche

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Reference37 articles.

1. Qualitative structure-metabolism relationships in the hydrolysis of carbamates

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3. Metabolic Pathways of Agrochemicals: Insecticides and fungicides , ed. T. Roberts , D. Hutson , P. W. Lee , P. H. Nicholls and J. R. Plimmer , Royal Society of Chemistry , 1998

4. Combinatorial chemistry — applications of light-directed chemical synthesis

5. M. M. Mehndiratta , S.Pandey and T.Kuntzer , Cochrane db. Syst. Rev. , 2014, CD006986

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