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首页> 外文期刊>Mini reviews in medicinal chemistry >Small Molecules as Potent Protein Tyrosine Phosphatase 1B (PTP1B) Inhibitors Documented in Patents from 2009 to 2013
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Small Molecules as Potent Protein Tyrosine Phosphatase 1B (PTP1B) Inhibitors Documented in Patents from 2009 to 2013

机译:2009年至2013年专利中记载的小分子作为强力蛋白酪氨酸磷酸酶1B(PTP1B)抑制剂

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摘要

Diabetes mellitus, including type 1 and type 2 diabetes mellitus (2-DM) are the main threats to human health in the worldwide. Protein tyrosine phosphatase 1B (PTP1B) is a promising molecular level legitimate therapeutic target in the effective management of 2-DM. For the search of potent PTP1B inhibitors, much investigation has revealed a large number of small-molecule compounds obtained from natural sources or prepared by synthesis/semi-synthesis with various skeletons and promising anti-PTP1B activities in the treatment of 2-DM. Although some reviews on the development of PTP1B inhibitors have been published, they were mainly concentrated on the results reported in journal articles. In this review, we will provide an overview of the developments of the potent PTP1B inhibitors claimed in recent patents during the past five years (2009-2013) with their structural features and biological features, as well as the structure-activity relationships (SARs) and strategies for finding potent and specific PTP1B inhibitors. This paper will provide valuable information for understanding the current anti-PTP1B investigation and developing potent PTP1B inhibitors as treating 2-DM drugs.
机译:糖尿病,包括1型和2型糖尿病(2-DM),是全球范围内对人类健康的主要威胁。蛋白酪氨酸磷酸酶1B(PTP1B)是有效治疗2-DM的分子水平合法治疗目标。为了寻找有效的PTP1B抑制剂,许多研究表明,有大量的小分子化合物是从天然来源获得或通过合成/半合成制备的,具有各种骨架,并且在治疗2-DM中具有良好的抗PTP1B活性。尽管已经发表了有关PTP1B抑制剂开发的一些评论,但它们主要集中在期刊文章中报道的结果上。在本综述中,我们将概述过去五年(2009-2013年)在最近的专利中主张的强效PTP1B抑制剂的发展情况,以及它们的结构特征和生物学特征,以及结构-活性关系(SAR)和寻找有效和特异性PTP1B抑制剂的策略。本文将为了解当前的抗PTP1B研究和开发有效的PTP1B抑制剂作为治疗2-DM药物提供有价值的信息。

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