Synthesis and Mechanism of Action of Novel Thiocarbamate Inhibitors of Human Leukocyte Elastase.

Sky Li-Pan Z, Joshi, Digenis
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引用次数: 2

Abstract

Several peptidyl thiocarbamate inhibitors of human leukocyte elastase were synthesized in the molecular weight range of 700-800. Two different sequences with lysine at the P(3) and ornithine at the P(4) positions were synthesized. Most of the inhibitors with large molecular weights showed high inhibitory capacity with Ki values as low as 10(-8) M. Compounds immobilized on poly,alpha,beta-[N-(2-hydroxyethyl)-d,l-aspartamide] (PHEA) polymers with an average molecular weight of 36,000 showed higher inhibitory capacity than their free forms.
新型人白细胞弹性酶硫氨基甲酸酯抑制剂的合成及作用机制研究。
合成了几种人白细胞弹性酶肽基硫氨基甲酸酯抑制剂,分子量在700 ~ 800之间。合成了两个不同的P(3)位赖氨酸和P(4)位鸟氨酸的序列。大分子量抑制剂Ki值低至10(-8)m,平均分子量为36,000的聚α, β -[N-(2-羟乙基)-d,l-阿斯巴酰胺](PHEA)聚合物上固定的化合物比其自由形式具有更高的抑制能力。
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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