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Quinoxalines Potential to Target Pathologies.
Tristán-Manzano, María; Guirado, Antonio; Martínez-Esparza, María; Gálvez, Jesús; García-Peñarrubia, Pilar; Ruiz-Alcaraz, Antonio J.
Afiliação
  • Ruiz-Alcaraz AJ; Department of Biochemistry, Molecular Biology B and Immunology, Faculty of Medicine, Murcia University, 30100 Murcia, Spain. ajruiz@um.es.
Curr Med Chem ; 22(26): 3075-108, 2015.
Article em En | MEDLINE | ID: mdl-26264925
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.
Assuntos
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Base de dados: MEDLINE Assunto principal: Quinoxalinas / Descoberta de Drogas / Terapia de Alvo Molecular Idioma: En Ano de publicação: 2015 Tipo de documento: Article
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Base de dados: MEDLINE Assunto principal: Quinoxalinas / Descoberta de Drogas / Terapia de Alvo Molecular Idioma: En Ano de publicação: 2015 Tipo de documento: Article