Pyridazinone-substituted benzenesulfonamides display potent inhibition of membrane-bound human carbonic anhydrase IX and promising antiproliferative activity against cancer cell lines-Reference-Cited by-同舟云学术

Pyridazinone-substituted benzenesulfonamides display potent inhibition of membrane-bound human carbonic anhydrase IX and promising antiproliferative activity against cancer cell lines

Published:2019-04 Issue: Volume:168 Page:301-314
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Krasavin Mikhail^ORCID,Shetnev Anton^ORCID,Baykov Sergey^ORCID,Kalinin Stanislav,Nocentini Alessio^ORCID,Sharoyko Vladimir,Poli Giulio,Tuccinardi Tiziano^ORCID,Korsakov Mikhail,Tennikova Tatiana B.,Supuran Claudiu T.^ORCID

Funder

the Russian Federation Government Megagrant

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference48 articles.

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2. Multiple binding modes of inhibitors to carbonic anhydrases: how to design specific drugs targeting 15 different isoforms?;Alterio;Chem. Rev.,2012

3. Carbonic anhydrase inhibitors and activators for novel therapeutic applications;Supuran;Future Med. Chem.,2011

4. The η-class carbonic anhydrases as drug targets for antimalarial agents;Supuran;Expert Opin. Ther. Targets,2015

5. Diuretics: from classical carbonic anhydrase inhibitors to novel applications of the sulfonamides;Supuran;Curr. Pharmaceut. Des.,2008

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