Deciphering the Mechanism of Human Carbonic Anhydrases Inhibition with Sulfocoumarins: Computational and Experimental Studies-Reference-Cited by-同舟云学术

Deciphering the Mechanism of Human Carbonic Anhydrases Inhibition with Sulfocoumarins: Computational and Experimental Studies

Published:2018-05-03 Issue:31 Volume:24 Page:7840-7844
ISSN:0947-6539
Container-title:Chemistry - A European Journal
language:en
Short-container-title:Chem. Eur. J.

Author:

Nocentini Alessio¹²,Carta Fabrizio²,Tanc Muhammet²,Selleri Silvia²,Supuran Claudiu T.²,Bazzicalupi Carla³,Gratteri Paola¹^ORCID

Affiliation:

1. Department NEUROFARBA-Pharmaceutical and nutraceutical section; Laboratory of Molecular Modeling Cheminformatics & QSAR; University of Firenze; via Ugo Schiff 6 50019 Sesto Fiorentino Italy

2. Department NEUROFARBA-Pharmaceutical and nutraceutical section; University of Firenze; via Ugo Schiff 6 50019 Sesto Fiorentino Italy

3. Department of Chemistry “U. Schiff”; University of Florence; Via della Lastruccia 3 50019 Sesto Fiorentino Italy

Funder

Seventh Framework Programme

Publisher

Wiley

Subject

General Chemistry,Catalysis,Organic Chemistry

Reference23 articles.

1. Sulfocoumarins (1,2-Benzoxathiine-2,2-dioxides): A Class of Potent and Isoform-Selective Inhibitors of Tumor-Associated Carbonic Anhydrases

2. 6-Substituted Sulfocoumarins Are Selective Carbonic Anhdydrase IX and XII Inhibitors with Significant Cytotoxicity against Colorectal Cancer Cells

3. Synthesis of 6-tetrazolyl-substituted sulfocoumarins acting as highly potent and selective inhibitors of the tumor-associated carbonic anhydrase isoforms IX and XII

4. Facile synthesis of coumarin bioisosteres—1,2-benzoxathiine 2,2-dioxides

5. Multiple Binding Modes of Inhibitors to Carbonic Anhydrases: How to Design Specific Drugs Targeting 15 Different Isoforms?

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