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Synthesis and biological activity of substance P analogues.

作者信息

Haro I, Torres J L, Valencia G, García-Antón J M, Reig F

机构信息

Laboratory of Peptides, Centre for Research and Development (C.S.I.C.), Barcelona, Spain.

出版信息

Int J Pept Protein Res. 1989 May;33(5):335-9. doi: 10.1111/j.1399-3011.1989.tb00690.x.

DOI:10.1111/j.1399-3011.1989.tb00690.x
PMID:2475448
Abstract

The synthesis of the hexapeptide [Glu6]SP6-11 and its glycosylated analogue at the Glu6 gamma-carboxyl position by solution procedures according to several strategies is discussed. The biological activity of SP, [Glu6]SP6-11 (VI) and [Glu(beta-D-Glcp)6]SP6-11 (VIII) have been determined and compared to SP by the GPI and RVD assays. The introduction of a beta-D-glucopyranosyl moiety at the sixth position of the [Glu6]SP6-11 did not affect to a great extent the in vitro activity pattern of the parent hexapeptide.

摘要

相似文献

1
Synthesis and biological activity of substance P analogues.
Int J Pept Protein Res. 1989 May;33(5):335-9. doi: 10.1111/j.1399-3011.1989.tb00690.x.
2
Pseudopeptide analogues of substance P and leucine enkephalinamide containing the psi (CH2O) modification: synthesis and biological activity.含有ψ(CH2O)修饰的P物质和亮氨酸脑啡肽酰胺的拟肽类似物:合成与生物活性
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In vitro activity and selectivity of glucosidic SP(6-11) analogues.葡糖苷酸SP(6 - 11)类似物的体外活性和选择性
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A synthetic glycopeptide of substance P analogue (SP6-11) with enhanced NK-1 receptor specificity.一种具有增强的NK-1受体特异性的P物质类似物(SP6-11)的合成糖肽。
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Synthesis and biological activity of substance P C-terminal hexapeptide and heptapeptide analogues.P物质C末端六肽和七肽类似物的合成及生物活性
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Synthesis and some biological properties of the hexapeptide analog of substance P with a C-terminal thioamide group.
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Synthesis of potent agonists of substance P by replacement of Met11 with Glu(OBzl) and N-terminal glutamine with Glp of the C-terminal hexapeptide and heptapeptide of substance P.
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