Design and Synthesis of Novel Arylketo-containing P1-P3 Linked Macro-cyclic BACE-1 Inhibitors.

Q2 Pharmacology, Toxicology and Pharmaceutics
Open Medicinal Chemistry Journal Pub Date : 2015-03-31 eCollection Date: 2015-01-01 DOI:10.2174/1874104501509010013
Veronica Sandgren, Oscar Belda, Ingemar Kvarnström, Jimmy Lindberg, Bertil Samuelsson, Anders Dahlgren
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引用次数: 1

Abstract

A series of arylketo-containing P1-P3 linked macrocyclic BACE-1 inhibitors were designed, synthesized, and compared with compounds with a previously known and extensively studied corresponding P2 isophthalamide moiety with the aim to improve on permeability whilst retaining the enzyme- and cell-based activities. Several inhibitors displayed substantial increases in Caco-2 cell-based permeability compared to earlier synthesized inhibitors and notably also with retained activities, showing that this approach might yield BACE-1 inhibitors with improved properties.

Abstract Image

Abstract Image

Abstract Image

新型芳基酮类P1-P3连接大环BACE-1抑制剂的设计与合成
设计、合成了一系列含芳基酮P1-P3连接的大环BACE-1抑制剂,并与先前已知和广泛研究的相应P2异眼酰胺片段的化合物进行了比较,目的是在保持酶和细胞活性的同时提高其通透性。与早期合成的抑制剂相比,一些抑制剂显示出Caco-2细胞基通透性的显著增加,特别是保留了活性,表明这种方法可能产生性能更好的BACE-1抑制剂。
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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来源期刊
Open Medicinal Chemistry Journal
Open Medicinal Chemistry Journal Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
4.40
自引率
0.00%
发文量
4
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