Affiliation:
1. CEDECOR, Departamento de Quimica, Facultad de Ciencias Exactas, Universidad Nacional de La Plata, 47 y 115 (1900) La Plata, Argentina
Abstract
Attachment of different tails to the well-known carbonic anhydrase (CA) pharmacophores
has led to the development of several new CA inhibitors (CAIs). A very good example
of such “tails” is constituted by carbohydrates, which represent a wide range of chemotypes,
leading thus to a high number of new CAIs. In the last years, several C-cinnamoyl glycosides
containing different scaffolds have been prepared and investigated as carbonic anhydrase
inhibitors, showing that some of them are very potent and selective CAIs. This article
will review the latest developments in the synthesis and biological activity of these Cglycosides.
Publisher
Bentham Science Publishers Ltd.
Subject
Pharmacology,Molecular Medicine,Drug Discovery,Biochemistry,Organic Chemistry
Cited by
5 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献