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Synthesis and anti-elastase properties of 6-amino-2-phenyl-4H-3,1-benzoxazin-4-one aminoacyl and dipeptidyl derivatives

机译:6-氨基-2-苯基-4H-3,1-苯并恶嗪-4-酮氨基酰基和二肽基衍生物的合成及抗弹性蛋白酶性能

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A series of 6-amino-2-phenyl-4H-3,1-benzoxazin-4-one aminoacyl and dipeptidyl derivatives, in which aminoacids and dipeptides are linked to the benzoxazinone moiety via an amide bond, were synthesized and tested in vitro for their inhibitory activity towards human leukocyte elastase (HLE). When compared to their values without inhibitors, the residual enzymatic activities decrease with time, indicating a time-dependent inhibition. The most potent inhibitions were obtained when Z-Arg-(Pmc), Z-Val-Phe. Z-Ala-Val or Z-Val-Ala are linked to the 6-amino group. Twenty-five new compounds were synthesized. (c) 2004 Elsevier SAS. All rights reserved.
机译:合成了一系列6-氨基-2-苯基-4H-3,1-苯并恶嗪-4-酮氨基酸和二肽衍生物,其中氨基酸和二肽通过酰胺键与苯并恶嗪酮部分相连,并进行了体外测试它们对人白细胞弹性蛋白酶(HLE)的抑制活性。与没有抑制剂的值相比,残留的酶活性随时间降低,表明时间依赖性抑制。当Z-Arg-(Pmc),Z-Val-Phe时,抑制作用最强。 Z-Ala-Val或Z-Val-Ala与6-氨基连接。合成了二十五个新化合物。 (c)2004年Elsevier SAS。版权所有。

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