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2-(硫)代脲苯并噻唑的合成及生物学意义。

Synthesis and Biological Importance of 2-(thio)ureabenzothiazoles.

机构信息

Laboratorio de Biofísica y Biocatálisis, Sección de Estudios de Posgrado e Investigación, Escuela Superior de Medicina, Instituto Politécnico Nacional, Plan de San Luis y Salvador Díaz Mirón s/n, Casco de Santo Tomás, Mexico City 11340, Mexico.

Instituto Politécnico Nacional-UPIBI, Laboratorio de Química Supramolecular y Nanociencias, Av. Acueducto s/n, Barrio la Laguna Ticomán, Mexico City 07340, Mexico.

出版信息

Molecules. 2022 Sep 19;27(18):6104. doi: 10.3390/molecules27186104.

Abstract

The (thio)urea and benzothiazole (BT) derivatives have been shown to have a broad spectrum of biological activities. These groups, when bonded, result in the 2-(thio)ureabenzothizoles (TBT and UBT), which could favor the physicochemical and biological properties. UBTs and TBTs are compounds of great importance in medicinal chemistry. For instance, Frentizole is a UBT derivative used for the treatment of rheumatoid arthritis and systemic lupus erythematosus. The UBTs Bentaluron and Bethabenthiazuron are commercial fungicides used as wood preservatives and herbicides in winter corn crops. On these bases, we prepared this bibliography review, which covers chemical aspects of UBTs and TBTs as potential therapeutic agents as well as their studies on the mechanisms of a variety of pharmacological activities. This work covers synthetic methodologies from 1935 to nowadays, highlighting the most recent approaches to afford UBTs and TBTs with a variety of substituents as illustrated in 42 schemes and 13 figures and concluded with 187 references. In addition, this interesting review is designed on chemical reactions of 2-aminobenzothiazoles (2ABTs) with (thio)phosgenes, iso(thio)cyanates, 1,1'-(thio)carbonyldiimidazoles [(T)CDI]s, (thio)carbamoyl chlorides, and carbon disulfide. This topic will provide information of utility for medicinal chemists dedicated to the design and synthesis of this class of compounds to be tested with respect to their biological activities and be proposed as new pharmacophores.

摘要

(硫)脲和苯并噻唑(BT)衍生物已被证明具有广泛的生物活性。这些基团结合在一起会形成 2-(硫)脲苯并噻唑(TBT 和 UBT),这可能有利于理化性质和生物性质。UBTs 和 TBTs 是药物化学中非常重要的化合物。例如,Frentizole 是一种用于治疗类风湿关节炎和系统性红斑狼疮的 UBT 衍生物。UBTs Bentaluron 和 Bethabenthiazuron 是商业性杀真菌剂,用作木材防腐剂和冬季玉米作物中的除草剂。基于此,我们准备了这份文献综述,涵盖了 UBTs 和 TBTs 作为潜在治疗剂的化学方面,以及它们在各种药理学活性机制方面的研究。这项工作涵盖了从 1935 年至今的合成方法,重点介绍了最近的方法,以提供具有各种取代基的 UBTs 和 TBTs,如图 42 个方案和 13 个图所示,并以 187 个参考文献结尾。此外,这个有趣的综述是基于 2-氨基苯并噻唑(2ABTs)与(硫)光气、异(硫)氰酸酯、1,1'-(硫)羰基二咪唑 [(T)CDI]、(硫)碳酰氯和二硫化碳的化学反应设计的。这个主题将为致力于设计和合成这类化合物的药物化学家提供有用的信息,以便对其生物活性进行测试,并作为新的药效团进行提出。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/753d/9502297/b5069b6fb89a/molecules-27-06104-g001.jpg

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