| Literature DB >> 26264925 |
María Tristán-Manzano, Antonio Guirado, María Martínez-Esparza, Jesús Gálvez, Pilar García-Peñarrubia, Antonio J Ruiz-Alcaraz1.
Abstract
The study of quinoxalines has increased immeasurably during the last two decades, due firstly to their relatively simple chemical synthesis, which has generated a vast variety of compounds with diverse structural modifications, and secondly, to the wide therapeutic potential and biological activities exhibited by this family of compounds. Quinoxalines constitute a rising biomedical class of low-molecular weight heterocyclic compounds with potential functions as antitumour, anti-inflammatory, antibacterial, antiviral, antifungal, antiparasitic and antidiabetic agents, as well as being of interest for the potential treatment of glaucoma, insomnia, cardiovascular and neurological diseases, among others. However, a deeper knowledge of the molecular targets of quinoxalines that fulfil a key role in certain pathologies is required for the development of new and more specific drugs through a rational design strategy to avoid undesirable side effects. In the present review, we summarize the most important molecular targets of the quinoxaline derivatives discovered to date, thus providing a first reference index for researchers to identify the potential targets of their quinoxalines derived collections, which could facilitate the development of new quinoxaline- based therapies.Entities:
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Year: 2015 PMID: 26264925 DOI: 10.2174/0929867322666150812144104
Source DB: PubMed Journal: Curr Med Chem ISSN: 0929-8673 Impact factor: 4.530