Human carbonic anhydrase inhibitory profile of mono- and bis-sulfonamides synthesized via a direct sulfochlorination of 3- and 4-(hetero)arylisoxazol-5-amine scaffolds-Reference-Cited by-同舟云学术

Human carbonic anhydrase inhibitory profile of mono- and bis-sulfonamides synthesized via a direct sulfochlorination of 3- and 4-(hetero)arylisoxazol-5-amine scaffolds

Published:2017-03 Issue:6 Volume:25 Page:1914-1925
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Krasavin Mikhail,Korsakov Mikhail,Zvonaryova Zhanna,Semyonychev Evgenii,Tuccinardi Tiziano,Kalinin Stanislav,Tanç Muhammet,Supuran Claudiu T.

Funder

Russian Scientific Fund

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference23 articles.

1. Design of Zinc Binding Functions for Carbonic Anhydrase Inhibitors

2. How many carbonic anhydrase inhibition mechanisms exist?

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

4. Selection of Carbonic Anhydrase IX Inhibitors from One Million DNA-Encoded Compounds

5. Carbonic anhydrases: novel therapeutic applications for inhibitors and activators

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