A Pharmacological Overview and Recent Patent of Triazine Scaffold in Drug Development: A Review

IF 1.7 4区 化学 Q3 CHEMISTRY, ORGANIC Current organic synthesis Pub Date : 2024-09-10 DOI:10.2174/0115701794272212240307092318
Pragya Dubey, Dharam Pal Pathak, Garima Chauhan, Faraat Ali
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Abstract

<p>The triazine moiety holds a special and very important position in the field of medicinal chemistry owing to its enormous biological and pharmacological potential. Over eras, triazine scaffolds have been investigated for synthesizing novel molecules that may be used for the treatment of different types of pathological conditions, such as infections, cancer, inflammation etc. A vast number of lead molecules have been established from the triazine moiety. The triazine fused with numerous heterocyclic rings, such as pyrrole, benzimidazole, indole, imidazole, carbazole, etc., have formed various bicyclic with pharmacological actions. The triazines display a wide range of activities, and synthesizing various marketable medicines that hold triazine moiety has made the attention of chemists worldwide grow over the years in the moiety. In this review article, the commercially available compound containing triazine has been presented, and an attempt has been made to collect the works reported, mostly in the past decade, by numerous scientists, related to the structural differences amongst the triazine analogues giving antitumor, and antimicrobial and other activities. </p><p> The objective of this review article was to outline the current information on triazines and their derivatives with respect to their biological potential and various pharmacological activities. </p><p> The summary of this review article would be helpful and describe the function and activity of the moiety to bring up-to-date the scientists working in the direction of designing and synthesising novel lead molecules for the treatment of different types of disease with the current molecules that have been synthesized from the triazine scaffold.</p>
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药物开发中的三嗪支架药理学概述和最新专利:综述
<p>由于具有巨大的生物学和药理学潜力,三嗪分子在药物化学领域占有非常重要的特殊地位。多年来,人们一直在研究用三嗪支架合成可用于治疗感染、癌症、炎症等不同病症的新型分子。目前已从三嗪分子中发现了大量先导分子。三嗪与许多杂环(如吡咯、苯并咪唑、吲哚、咪唑、咔唑等)融合,形成了各种具有药理作用的双环化合物。三嗪类化合物具有广泛的活性,多年来,合成含有三嗪分子的各种上市药物使全世界的化学家越来越关注这一分子。在这篇综述文章中,介绍了含有三嗪的市售化合物,并尝试收集了许多科学家在过去十年中报告的与三嗪类似物结构差异有关的工作,这些类似物具有抗肿瘤、抗菌和其他活性。</p><p>这篇综述文章的摘要将有助于描述三嗪分子的功能和活性,使从事设计和合成新型先导分子方向工作的科学家与时俱进,利用目前从三嗪支架合成的分子治疗不同类型的疾病;
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来源期刊
Current organic synthesis
Current organic synthesis 化学-有机化学
CiteScore
3.40
自引率
5.60%
发文量
86
审稿时长
6-12 weeks
期刊介绍: Current Organic Synthesis publishes in-depth reviews, original research articles and letter/short communications on all areas of synthetic organic chemistry i.e. asymmetric synthesis, organometallic chemistry, novel synthetic approaches to complex organic molecules, carbohydrates, polymers, protein chemistry, DNA chemistry, supramolecular chemistry, molecular recognition and new synthetic methods in organic chemistry. The frontier reviews provide the current state of knowledge in these fields and are written by experts who are internationally known for their eminent research contributions. The journal is essential reading to all synthetic organic chemists. Current Organic Synthesis should prove to be of great interest to synthetic chemists in academia and industry who wish to keep abreast with recent developments in key fields of organic synthesis.
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A Pharmacological Overview and Recent Patent of Triazine Scaffold in Drug Development: A Review Development of a Suitable Method for the Synthesis of New Thiadiazoles Using Hydrazonoyl Halides Synthesis of Heterocyclic Sulfonium Triflates by Cu-Catalyzed Selective Sarylation with Aryl(mesityl)iodonium Salts Co2(CO)8 as a CO-source for Pd-catalyzed Carbonylations: An Update Synthesis and Characterization of Novel Polythiadiazoles from Bis-hydrazonoyl Dichlorides and Bis-(methyl-2-arylidene hydrazone carbodithioates)
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