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新型 HIV-1 非核苷类逆转录酶抑制剂:专利研究综述(2011-2014)

Novel HIV-1 non-nucleoside reverse transcriptase inhibitors: a patent review (2011-2014).

机构信息

Shandong University, School of Pharmaceutical Sciences, Department of Medicinal Chemistry, Key Laboratory of Chemical Biology (Ministry of Education) , 44, West Culture Road, 250012, Jinan, Shandong , PR China +86 531 88382005 ; +86 531 88382731 ;

出版信息

Expert Opin Ther Pat. 2014 Nov;24(11):1199-227. doi: 10.1517/13543776.2014.964685. Epub 2014 Oct 14.

DOI:10.1517/13543776.2014.964685
PMID:25313716
Abstract

INTRODUCTION

There is a continuous need for next-generation non-nucleoside RT inhibitors (NNRTIs) with different resistance profiles, improved safety, excellent tolerability, and favorable physicochemical properties.

AREAS COVERED

In this review we intend to narrate a general and cutting-edge overview of current state of NNRTI patents during the 2011-2014 (June) period and future perspectives. Particular focus is placed on the highlighting of some emerging medicinal chemistry principles and insights in the discovery and development of NNRTIs.

EXPERT OPINION

The development of effective NNRTIs is moving on from trial-and-error approaches to sophisticated subconscious strategies. Several newly emerging structure-based virtual screening methodologies (such as Monte Carlo free energy perturbation calculations) or new drug design insights, such as taking full use of the specific noncovalent reverse transcriptase/NNRTIs interactions, stereochemical diversity-oriented conformational restriction, novel strategies to enhance solubility and early absorption, distribution, metabolism, excretion, and toxicity (ADMET) assessment, will continue to evolve to complement the classical NNRTIs discovery approaches (structure-based core-refining and substituents-decorating).

摘要

简介

需要不断开发具有不同耐药谱、更高安全性、良好耐受性和理想理化性质的下一代非核苷类逆转录酶抑制剂(NNRTIs)。

涵盖领域

本文综述了 2011 年至 2014 年(6 月)期间 NNRTI 专利的现状和未来展望,概述了 NNRTIs 发现和开发过程中新兴药物化学原理和研究进展。

专家意见

有效的 NNRTIs 的开发正从试错方法向复杂的潜意识策略转变。几种新出现的基于结构的虚拟筛选方法(如蒙特卡罗自由能微扰计算)或新药设计思路,如充分利用特定的非共价逆转录酶/NNRTIs 相互作用、立体化学多样性定向构象限制、提高溶解度和早期吸收、分布、代谢、排泄和毒性(ADMET)评估的新策略,将继续发展,以补充经典的 NNRTIs 发现方法(基于结构的核心改进和取代基修饰)。

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