采用 1,2,4-三唑类似物的商业化制剂的合成方法、SAR 和药理学

IF 1.9 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY ChemistrySelect Pub Date : 2024-11-18 DOI:10.1002/slct.202404350
Research Student Sucheta Singh, Assistant Professor Meenakshi Kaira, Research Student Hrithik Dey, Dr. Kailash C. Pandey, Dr. Research Scientist Sumit Tahlan, Research Student Kuldeep Singh
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引用次数: 0

摘要

由于三唑具有独特的结构特征和广泛的应用范围,药物化学领域对三唑的兴趣明显增加。其合成方法的多样性促进了化合物库的建立,这些化合物具有显著的药理活性,包括抗病毒、抗癫痫、抗焦虑、催眠/镇静剂、抗癌、抗真菌和抗抑郁活性。文献中记载了几种生成 1,2,4-三唑衍生物的技术。含 1,2,4-三唑的制剂的药理作用机制已得到阐明和明确。除了回顾现有的上市制剂,本综述还探讨了该领域的新趋势和创新。本综述从一个全面的角度阐述了三唑类药物在影响当代研究、促进创新和推动技术进步方面的重要性。
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Synthetic Methodology, SAR and Pharmacology of Commercialized Preparations Employing 1, 2, 4-Triazole Analogues

The domain of medicinal chemistry has witnessed a notable surge of interest in triazoles owing to their unique structural characteristics and wide range of applications. The versatility of their synthesis methods has facilitated the creation of compound libraries with remarkable pharmacological activities, including antiviral, antiepileptic, anxiolytic, hypnotic/sedatives anticancer, antifungal, and antidepressant activities. Several techniques have been documented in the literature for generating 1,2,4-triazole derivatives. The mechanisms governing the pharmacological effects of the formulations containing 1,2,4-triazoles were elucidated and made clear. In addition to reviewing existing marketed formulations, this review explores emerging trends and innovations in this field. This review offers a comprehensive perspective on the importance of triazoles for influencing contemporary research, fostering innovation, and driving technological progress.

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来源期刊
ChemistrySelect
ChemistrySelect Chemistry-General Chemistry
CiteScore
3.30
自引率
4.80%
发文量
1809
审稿时长
1.6 months
期刊介绍: ChemistrySelect is the latest journal from ChemPubSoc Europe and Wiley-VCH. It offers researchers a quality society-owned journal in which to publish their work in all areas of chemistry. Manuscripts are evaluated by active researchers to ensure they add meaningfully to the scientific literature, and those accepted are processed quickly to ensure rapid online publication.
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