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螺环杂环甾体的合成与药物化学

Syntheses and medicinal chemistry of spiro heterocyclic steroids.

作者信息

Romero-Hernández Laura L, Ahuja-Casarín Ana Isabel, Merino-Montiel Penélope, Montiel-Smith Sara, Vega-Báez José Luis, Sandoval-Ramírez Jesús

机构信息

Facultad de Ciencias Químicas, Benemérita Universidad Autónoma de Puebla, Ciudad Universitaria, 72570, Puebla, Pue., México.

出版信息

Beilstein J Org Chem. 2024 Jul 24;20:1713-1745. doi: 10.3762/bjoc.20.152. eCollection 2024.

Abstract

There is compelling evidence that incorporating a heterocyclic moiety into a steroid can alter its pharmacological and pharmacokinetic properties, driving intense interest in the synthesis of such hybrids among research groups. In this review, we present an overview of recent synthetic methodologies, spanning the period from 2000 to 2023, for the preparation of spiro heterocyclic steroids. The compounds surveyed encompass four-, five-, six-, and seven-membered heterocycles appended to various positions of steroidal backbones, with spirocycles containing oxygen, nitrogen, and sulfur atoms being predominant. The outlined synthetic procedures emphasize the pivotal steps for constructing the heterocycles, often accompanied by a detailed account of the overall synthesis pathway. The review encompasses innovative compounds, including bis-steroids linked by a spiro heterocycle and steroids conjugated to heterocyclic moieties containing three or more (hetero)cycles. Moreover, many compounds are accompanied by data on their biological activities, such as antiproliferative, antimalarial, antimicrobial, antifungal, steroid antagonist, and enzyme inhibition, among others, aimed at furnishing pertinent insights for the future design of more potent and selective drugs.

摘要

有令人信服的证据表明,将杂环部分引入甾体可以改变其药理和药代动力学性质,这引发了研究团队对合成此类杂化物的浓厚兴趣。在本综述中,我们概述了2000年至2023年期间用于制备螺杂环甾体的最新合成方法。所调查的化合物包括连接在甾体骨架不同位置的四元、五元、六元和七元杂环,其中以含氧、氮和硫原子的螺环为主。所概述的合成程序强调了构建杂环的关键步骤,通常还详细说明了整个合成途径。该综述涵盖了创新化合物,包括通过螺杂环连接的双甾体以及与含有三个或更多(杂)环的杂环部分共轭的甾体。此外,许多化合物还伴有其生物活性数据,如抗增殖、抗疟疾、抗菌、抗真菌、甾体拮抗剂和酶抑制等,旨在为未来设计更有效和更具选择性的药物提供相关见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a90/11285062/a11b3a7d3243/Beilstein_J_Org_Chem-20-1713-g002.jpg

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