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生物活性二酮哌嗪类化合物的研究进展:专利述评。

Developments around the bioactive diketopiperazines: a patent review.

机构信息

Ocean University of China, School of Medicine and Pharmacy, Key Laboratory of Marine Drugs, Ministry of Education of China , Qingdao 266003 , People's Republic of China +86 532 82031268 ; +86 532 82031268 ;

出版信息

Expert Opin Ther Pat. 2013 Nov;23(11):1415-33. doi: 10.1517/13543776.2013.828036. Epub 2013 Aug 21.

Abstract

INTRODUCTION

2,5-Diketopiperazines (DKPs) are cyclic dipeptides from two amino acids with or without further structural modifications in DKP nucleus. These DKPs demonstrated attractive bioactive diversity and potential in drug discovery.

AREAS COVERED

This review summarized those bioactive DKPs in patents, and provided the analysis of the structure types (N-substitution, secondary cyclization, isopentenylation, S-substitution, dehydrogenation, and dimerization) and bioactivities including anti-tumor, neuroprotective, immune and metabolic regulatory, oxytocin inhibitory and anti-inflammatory effects, antibiotic activity, PAF inhibition, inhibition of plasminogen activator and T-cell mediated immunity, and insecticidal activity, etc.

EXPERT OPINION

Though DKPs did not show very complicated chemical structures, their rigid structure, chiral nature and varied side chains led to their various medicinal applications.

摘要

简介

2,5-二酮哌嗪(DKP)是由两个氨基酸组成的环状二肽,其核心结构中可能带有或不带有进一步的结构修饰。这些 DKP 展示了吸引人的生物活性多样性和在药物发现方面的潜力。

涵盖领域

本综述总结了专利中的那些具有生物活性的 DKP,并对其结构类型(N-取代、二级环化、异戊烯基化、S-取代、脱氢和二聚化)和生物活性进行了分析,包括抗肿瘤、神经保护、免疫和代谢调节、催产素抑制和抗炎作用、抗生素活性、PAF 抑制、纤溶酶原激活物抑制和 T 细胞介导的免疫抑制以及杀虫活性等。

专家意见

尽管 DKP 没有表现出非常复杂的化学结构,但它们刚性的结构、手性性质和多样的侧链导致了它们在各种医药应用中的多样性。

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