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色烯吡啶骨架:药物设计中的一个优势平台。

The Chromenopyridine Scaffold: A Privileged Platform in Drug Design.

机构信息

Chemistry Centre, School of Sciences, University of Minho, Gualtar Campus, 4715-303 Braga, Portugal.

Centre for Textile Science and Technology (2C2T), University of Minho, Azurém Campus, 4800-058 Guimarães, Portugal.

出版信息

Molecules. 2024 Jun 25;29(13):3004. doi: 10.3390/molecules29133004.

DOI:10.3390/molecules29133004
PMID:38998955
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11243271/
Abstract

The chromenopyridine scaffold represents an important class of heterocyclic compounds exhibiting a broad spectrum of biological properties. This review describes novel and efficient procedures for the synthesis of this scaffold. Herein, several methods were detailed and grouped according to their starting material (e.g., salicylaldehydes, chromones, chromanones and coumarins) and respective biological activity, when reported. This review highlights the potential of the reported synthetic strategies for preparing chromenopyridine derivatives with promising biological activity, paving the way for further developments in drug discovery.

摘要

色烯并吡啶骨架代表了一类重要的杂环化合物,具有广泛的生物活性。本文综述了该骨架的新型高效合成方法。本文详细描述了几种方法,并根据其起始原料(例如水杨醛、色酮、色满酮和香豆素)和报道的相应生物活性进行了分组。本文综述强调了所报道的合成策略在制备具有潜在生物活性的色烯并吡啶衍生物方面的潜力,为药物发现的进一步发展铺平了道路。

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Green Protocol for the Novel Synthesis of Thiochromeno[4,3-]pyridine and Chromeno[4,3-]pyridine Derivatives Utilizing a High-Pressure System.利用高压系统新型合成硫代色烯并[4,3 - ]吡啶和色烯并[4,3 - ]吡啶衍生物的绿色协议
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鉴定 5H-色烯并[3,4-c]吡啶和 6H-异色烯并[3,4-c]吡啶衍生物为强效和选择性双重 ROCK 抑制剂。
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Unravelling the anticancer potential of functionalized chromeno[2,3-b]pyridines for breast cancer treatment.解析功能化色烯并[2,3-b]吡啶类化合物在乳腺癌治疗中的抗癌潜力。
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Synthesis and biological evaluation of novel pyrazolo[3,4-b]pyridines as cis-restricted combretastatin A-4 analogues.新型吡唑并[3,4-b]吡啶类化合物的合成及生物评价作为顺式受限的康普瑞汀 A-4 类似物。
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First example of Azo-Sulfa conjugated chromene moieties: Synthesis, characterization, antimicrobial assessment, docking simulation as potent class I histone deacetylase inhibitors and antitumor agents.首例偶氮-磺胺类共轭色烯部分:合成、表征、抗菌评估、作为有效 I 类组蛋白去乙酰化酶抑制剂和抗肿瘤药物的对接模拟。
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