Inhibition of α-, β-, γ-, and δ-carbonic anhydrases from bacteria and diatoms with N′-aryl-N-hydroxy-ureas-Reference-Cited by-同舟云学术

Inhibition of α-, β-, γ-, and δ-carbonic anhydrases from bacteria and diatoms with N′-aryl-N-hydroxy-ureas

Published:2018-01-01 Issue:1 Volume:33 Page:1194-1198
ISSN:1475-6366
Container-title:Journal of Enzyme Inhibition and Medicinal Chemistry
language:en
Short-container-title:Journal of Enzyme Inhibition and Medicinal Chemistry

Author:

Berrino Emanuela¹,Bozdag Murat¹,Del Prete Sonia¹²,Alasmary Fatmah A. S.³,Alqahtani Linah S.³⁴,AlOthman Zeid³,Capasso Clemente²,Supuran Claudiu T.¹³^ORCID

Affiliation:

1. Dipartimento Neurofarba, Sezione di Scienze Farmaceutiche e Nutraceutiche, Università degli Studi di Firenze, Florence, Italy;

2. CNR, Istituto di Bioscienze e Biorisorse, Napoli, Italy;

3. Department of Chemistry, College of Science, King Saud University, Riyadh, Saudi Arabia;

4. Department of Chemistry, King Faisal University, Alahsa, Saudi Arabia

Funder

DSFP

King Saud University

Publisher

Informa UK Limited

Subject

Drug Discovery,Pharmacology,General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/14756366.2018.1490733

Reference24 articles.

1. Hydroxyurea is a carbonic anhydrase inhibitor

2. Carbonic anhydrases: from biomedical applications of the inhibitors and activators to biotechnological use for CO2 capture

3. Advances in structure-based drug discovery of carbonic anhydrase inhibitors

4. Are Carbonic Anhydrases Suitable Targets to Fight Protozoan Parasitic Diseases?

5. Bacterial, fungal and protozoan carbonic anhydrases as drug targets

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