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首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >N-(3-(4-Hydroxyphenyl)-propenoyl)-amino acid tryptamides as SIRT2 inhibitors.
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N-(3-(4-Hydroxyphenyl)-propenoyl)-amino acid tryptamides as SIRT2 inhibitors.

机译:作为SIRT2抑制剂的N-(3-(4-羟基苯基)-丙烯酰基)-氨基酸类胰蛋白酶。

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摘要

A series of N-(3-(4-hydroxyphenyl)-propenoyl)-amino acid tryptamides was based on a previously reported new SIRT2 inhibitor from our group, and it was designed to study if the molecular size of the compound could be reduced. The most potent compounds, N-(3-(4-hydroxyphenyl)-propenoyl)-2-aminoisobutyric acid tryptamide and N-(3-(4-hydroxyphenyl)-propenoyl)-l-alanine tryptamide, were equipotent, 30% smaller in molecular weight, and slightly more selective (SIRT2/SIRT1) than the parent compound.
机译:一系列N-(3-(4-羟苯基)-丙烯酰基)-氨基酸类色胺类化合物是基于我们小组中先前报道的新型SIRT2抑制剂,旨在研究该化合物的分子大小是否可以降低。最有效的化合物N-(3-(4-羟苯基)-丙烯酰基)-2-氨基异丁酸色胺和N-(3-(4-羟苯基)-丙烯酰基)-1-丙氨酸色胺是等效的,小30%分子量,选择性(SIRT2 / SIRT1)比母体化合物略高。

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