含扩展P1取代基的羟乙基BACE-1抑制剂的设计与合成

Q2 Pharmacology, Toxicology and Pharmaceutics Open Medicinal Chemistry Journal Pub Date : 2013-03-08 Print Date: 2013-01-01 DOI:10.2174/1874104501307010001
Veronica Sandgren, Marcus Bäck, Ingemar Kvarnström, Anders Dahlgren
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引用次数: 28

摘要

以羟基乙烯为中心核的新型BACE-1抑制剂已经被开发出来。加入修饰的P1´和扩展的P1´取代基,目的是分别探索与BACE-1的S1´和S1- s3口袋的潜在相互作用。抑制剂的IC50值在纳摩尔范围内,即最有效的化合物为69 nM。还讨论了可能的抑制剂与酶的相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Design and Synthesis of Hydroxyethylene-Based BACE-1 Inhibitors Incorporating Extended P1 Substituents.
Novel BACE-1 inhibitors with a hydroxyethylene central core have been developed. Modified P1´ and extended P1 substituents were incorporated with the aim to explore potential interactions with the S1´ and the S1-S3 pocket, respectively, of BACE-1. Inhibitors were identified displaying IC50 values in the nanomolar range, i.e. 69 nM for the most potent compound. Possible inhibitor interactions with the enzyme are also discussed.
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来源期刊
Open Medicinal Chemistry Journal
Open Medicinal Chemistry Journal Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.40
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0.00%
发文量
4
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