Discovery of Novel Hydroxyimine-Tethered Benzenesulfonamides as Potential Human Carbonic Anhydrase IX/XII Inhibitors-Reference-Cited by-同舟云学术

Discovery of Novel Hydroxyimine-Tethered Benzenesulfonamides as Potential Human Carbonic Anhydrase IX/XII Inhibitors

Published:2023-05-08 Issue:6 Volume:14 Page:810-819
ISSN:1948-5875
Container-title:ACS Medicinal Chemistry Letters
language:en
Short-container-title:ACS Med. Chem. Lett.

Author:

Peerzada Mudasir Nabi¹^ORCID,Vullo Daniela²,Paoletti Niccolò²^ORCID,Bonardi Alessandro²,Gratteri Paola²^ORCID,Supuran Claudiu T.²^ORCID,Azam Amir¹

Affiliation:

1. Medicinal Chemistry and Drug Discovery Research Laboratory, Department of Chemistry, Jamia Millia Islamia, Jamia Nagar, New Delhi-110025, India

2. Department of NEUROFARBA, Section of Pharmaceutical and Nutraceutical Sciences, Laboratory of Molecular Modeling, Cheminformatics & QSAR, University of Florence, Polo Scientifico, Via U. Schiff 6, 50019 Sesto Fiorentino, Florence, Italy

Funder

Council of Scientific and Industrial Research, India

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acsmedchemlett.3c00094

Reference39 articles.

1. Carbonic Anhydrases as Drug Targets - An Overview

2. Carbonic Anhydrases: Role in pH Control and Cancer

3. Deciphering the key heterocyclic scaffolds in targeting microtubules, kinases and carbonic anhydrases for cancer drug development

4. Synthesis, characterization and biological evaluation of tertiary sulfonamide derivatives of pyridyl-indole based heteroaryl chalcone as potential carbonic anhydrase IX inhibitors and anticancer agents

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

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