Natural product hybrid and its superacid synthesized analogues: Dodoneine and its derivatives show selective inhibition of carbonic anhydrase isoforms I, III, XIII and XIV-Reference-Cited by-同舟云学术

Natural product hybrid and its superacid synthesized analogues: Dodoneine and its derivatives show selective inhibition of carbonic anhydrase isoforms I, III, XIII and XIV

Published:2013-07 Issue:13 Volume:21 Page:3790-3794
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Carreyre Hélène,Coustard Jean-Marie,Carré Grégoire,Vandebrouck Clarisse,Bescond Jocelyn,Ouédraogo Maurice,Marrot Jérôme,Vullo Daniella,Supuran Claudiu T.,Thibaudeau Sébastien

Funder

CNRS

University of Poitiers

Publisher

Elsevier BV

Subject

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

Reference67 articles.

1. Carbonic Anhydrase as a Model for Biophysical and Physical-Organic Studies of Proteins and Protein−Ligand Binding

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

3. Drug Design of Zinc-Enzyme Inhibitors: Functional, Structural, and Disease Applications;Supuran,2009

4. Entrapment of Carbon Dioxide in the Active Site of Carbonic Anhydrase II

5. Diuretics: From Classical Carbonic Anhydrase Inhibitors to Novel Applications of the Sulfonamides

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