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拓扑异构酶 I 抑制剂的专利研究综述(2016 年至今)。

A patent review of topoisomerase I inhibitors (2016-present).

机构信息

Departamento De Química Orgánica I, Facultad De Farmacia. Universidad Del País Vasco/Euskal Herriko Unibertsitatea (UPV/EHU), Vitoria-Gasteiz, Spain.

出版信息

Expert Opin Ther Pat. 2021 Jun;31(6):473-508. doi: 10.1080/13543776.2021.1879051. Epub 2021 Apr 29.

Abstract

INTRODUCTION

Topoisomerases are important targets for therapeutic improvement in the treatment of some diseases, including cancer. Inhibitors and poisons of topoisomerase I can limit the activity of this enzyme in its enzymatic cycle. This fact implies an anticancer effect of these drugs, since most cancer cells are characterized by both a higher activity of topoisomerase I and a higher replication rate compared to non-cancerous cells. Clinically approved inhibitors include camptothecin (CPT) and its derivatives. However, their limitations have encouraged different research groups to prepare new compounds, proof of which are the numerous research works and patents, some of them in the last five years.

AREAS COVERED

This review covers patent literature on topoisomerase I inhibitors and their application published between 2016-present.

EXPERT OPINION

The highest contribution toward patent development has been obtained from academics or small biotechnology companies. The most important fields of innovation include the preparation of prodrugs or inhibitors combined with other agents, as biocompatible polymers or antibodies. A promising development of topoisomerase I inhibitors is expected in the next years, directed to the treatment of diverse diseases, specifically toward different types of cancer and infectious diseases, among others.

摘要

简介

拓扑异构酶是治疗某些疾病(包括癌症)的治疗改进的重要靶点。拓扑异构酶 I 的抑制剂和毒物可以限制该酶在其酶循环中的活性。由于大多数癌细胞的拓扑异构酶 I 活性和复制率均高于非癌细胞,因此这些药物具有抗癌作用。临床上批准的抑制剂包括喜树碱(CPT)及其衍生物。但是,它们的局限性促使不同的研究小组准备新的化合物,这方面的证明是大量的研究工作和专利,其中一些是在过去五年中申请的。

涵盖领域

本综述涵盖了 2016 年至今发表的有关拓扑异构酶 I 抑制剂及其应用的专利文献。

专家意见

专利发展的最大贡献来自学术界或小型生物技术公司。创新最重要的领域包括前药或与其他药物(如生物相容性聚合物或抗体)联合的抑制剂的制备。预计在未来几年内,拓扑异构酶 I 抑制剂将有希望得到发展,用于治疗各种疾病,特别是针对不同类型的癌症和传染病等。

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