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THE PEPTOID SYNTHESIS FROM SOME AMINO ACID ANALOGS

机译:来自一些氨基酸类似物的肽合成

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摘要

Oligomeric N-substitued glycines(NSG)or "peptoids" are a novel class of polymer.In this study, four submonomers were synthesized for novel NSGs.These are 2- [(Triisopropylsilyl)oxy]ethylamine,Butyloxycarbonyl(Boc)-l,4-diaminobutane,sec-Butylamine,iso-Butylamine.These submonomers were successfully used for the preparation of oligo-peptoids by the conventional submonomer synthesis method.Peptoids or oligomers of N-substitued glycines which are not found in nature are a new class of polymers.Peptoids are based on a polyglycine backbone,in which the side chains are pendant groups of amide nitrogen rather than the a-carbon.Our purpose was to design,synthesize,purify and characterize the biophysical activity of polypeptoid-based biomimetics as hexamer peptoids which can replace important proteins in the body such as two lung surfactant proteins(SP-B and SP-C).
机译:寡聚N-拟合甘氨酸(NSG)或“肽”是一类新型聚合物。在这项研究中,为新颖的NSG合成了四个依赖器。 4-二氨基丁烷,二丁基胺,异丁胺。这些子体已成功地用于制备寡肽的寡肽。 聚合物。肽素是基于聚甘氨酸主链,其中侧链是酰胺氮而不是A-碳的吊坠。我们的目的是设计,合成,纯化,纯化和表征基于多肽的生物质学的生物物理活性,因为甲酰胺肽是甲酰胺肽肽杆菌肽的生物学活性 可以取代体内重要的蛋白质,例如两种肺表面活性剂蛋白(SP-B和SP-C)。

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