1,2,3-Triazines are a class of biologically active compounds that exhibit a broad spectrum of activities, including antibacterial, antifungal, antiviral, antiproliferative, analgesic and anti-inflammatory properties. This review, which covers the literature from the end of last century to 2016, treats, through a comprehensive, systematic approach, the 1,2,3-triazine and related benzo- and hetero-fused derivatives possessing antitumor activity. Their efficacy, combined with a simple synthesis confers to these molecules a great potential as scaffold for the development of antitumor compounds.

Cascioferro, S., Parrino, B., Spano', V., Carbone, A., Montalbano, A., Barraja, P., et al. (2017). Synthesis and antitumor activities of 1,2,3-triazines and their benzo- and heterofused derivatives. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 142, 74-86 [10.1016/j.ejmech.2017.06.003].

Synthesis and antitumor activities of 1,2,3-triazines and their benzo- and heterofused derivatives

CASCIOFERRO, Stella Maria;PARRINO, Barbara;SPANO', Virginia;CARBONE, Anna;MONTALBANO, Alessandra;BARRAJA, Paola;DIANA, Patrizia;CIRRINCIONE, Girolamo
2017-12-15

Abstract

1,2,3-Triazines are a class of biologically active compounds that exhibit a broad spectrum of activities, including antibacterial, antifungal, antiviral, antiproliferative, analgesic and anti-inflammatory properties. This review, which covers the literature from the end of last century to 2016, treats, through a comprehensive, systematic approach, the 1,2,3-triazine and related benzo- and hetero-fused derivatives possessing antitumor activity. Their efficacy, combined with a simple synthesis confers to these molecules a great potential as scaffold for the development of antitumor compounds.
15-dic-2017
Cascioferro, S., Parrino, B., Spano', V., Carbone, A., Montalbano, A., Barraja, P., et al. (2017). Synthesis and antitumor activities of 1,2,3-triazines and their benzo- and heterofused derivatives. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 142, 74-86 [10.1016/j.ejmech.2017.06.003].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10447/239356
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