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首页> 外文期刊>Chemical and Pharmaceutical Bulletin >Amino acids and peptides. XXXI. Preparation of analogs of the laminin-related peptide YIGSR and their inhibitory effect on experimental metastasis.
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Amino acids and peptides. XXXI. Preparation of analogs of the laminin-related peptide YIGSR and their inhibitory effect on experimental metastasis.

机译:氨基酸和肽。 XXXI。层粘连蛋白相关肽YIGSR的类似物的制备及其对实验转移的抑制作用。

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摘要

Analogs of a partial sequence peptide of laminin, i.e., Tyr-Ile-Gly-Ser-Arg (YIGSR) analogs and Cys-Asp-Pro-Gly-Tyr-Ile-Gly-Ser-Arg (CDPGYIGSR) analogs, were prepared by the solid-phase method and their inhibitory effects on experimental metastasis of B16-BL6 melanoma cells were examined. YIGSR analogs in which Ile was replaced by other hydrophobic amino acids (Met, Leu, Phe) were inhibitory. Cys-containing analogs of YIGSR were also prepared, but were less active than the parent peptide, YIGSR. Among them, CYIGSR was easily oxidized to form a disulfide bond. A Cys-containing YIGSR analog cyclized through a disulfide bond, cyclo(CYIGSRC)G, was prepared. The disulfide bond formation was performed on the resin by the silyl chloride-sulfoxide method and by the iodine oxidation method. The yield of the silyl chloride-sulfoxide method was much better than that of the iodine oxidation method.
机译:通过以下方法制备层粘连蛋白的部分序列肽的类似物,即Tyr-Ile-Gly-Ser-Arg(YIGSR)类似物和Cys-Asp-Pro-Gly-Tyr-Ile-Gly-Ser-Arg(CDPGYIGSR)类似物,研究了固相法及其对B16-BL6黑色素瘤细胞实验转移的抑制作用。其中Ile被其他疏水性氨基酸(Met,Leu,Phe)取代的YIGSR类似物具有抑制作用。还制备了YIGSR的含半胱氨酸的类似物,但是其活性低于亲本肽YIGSR。其中,CYIGSR很容易被氧化形成二硫键。制备了通过二硫键环(CYIGSRC)G环化的含Cys的YIGSR类似物。通过甲硅烷基氯-亚砜法和碘氧化法在树脂上形成二硫键。甲硅烷基氯-亚砜法的产率比碘氧化法好得多。

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