首页> 外文期刊>The Open Medicinal Chemistry Journal >Design and Synthesis of Novel Arylketo-containing P1-P3 Linked Macro-cyclic BACE-1 Inhibitors
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Design and Synthesis of Novel Arylketo-containing P1-P3 Linked Macro-cyclic BACE-1 Inhibitors

机译:新型含芳酮基的P1-P3连接的大环BACE-1抑制剂的设计与合成

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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.
机译:设计,合成了一系列含芳基酮基的P1-P3连接的大环BACE-1抑制剂,并与具有先前已知且经过广泛研究的相应P2间苯二酰胺部分的化合物进行了比较,目的是提高通透性,同时保留酶和细胞。基础活动。与早期合成的抑制剂相比,几种抑制剂显示出基于Caco-2细胞的通透性显着提高,并且特别是具有保留的活性,这表明该方法可能会产生具有改善性质的BACE-1抑制剂。

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