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Structure-activity relationships (SAR) of triazine derivatives: Promising antimicrobial agents

机译:三嗪衍生物的结构 - 活性关系(SAR):有前途的抗菌剂

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The emergence of drug resistance has created unmet medical need for the development of new classes of antibiotics. Innovation of new antibacterial agents with new mode of action remains a high priority universally. Triazines are six-membered, nitrogen-containing heterocyclic scaffold with a wide range of pharmaceutical properties such as antibacterial, antifungal, anticancer, antioxidants, antitubercular, antimalarial, anti-HIV, anticonvulsant, anti-inflammatory, antiulcer, and analgesic activities. The present review focuses on the recent developments in the area of medicinal chemistry to discover various chemical structures as potential antimicrobial agents and their structure-activity relationships (SAR) studies are also discussed for further rational design of this kind of derivatives. (C) 2019 Elsevier Masson SAS. All rights reserved.
机译:耐药性的出现为新类抗生素的发展创造了未满足的医疗需求。 具有新的行动模式的新抗菌剂的创新普遍优先于优先级。 三嗪是六元,含氮杂环支架,具有各种药物性质,如抗菌,抗真菌,抗癌,抗氧化剂,抗细胞,抗疟疾,抗艾滋病毒,抗惊厥药,抗炎,抗毒剂和镇痛活动。 本综述重点介绍了发现各种化学结构的最新发展,作为潜在的抗微生物剂及其结构 - 活性关系(SAR)研究也讨论了这种衍生物的进一步理性设计。 (c)2019年Elsevier Masson SAS。 版权所有。

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