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Synthesis and some pharmacological properties of [Glu(OMe)4]oxytocin and [Mpr1, Glu(OMe)4]oxytocin.

作者信息

Photaki I, Tzougraki C, Kotsira-Engonopoulos C

出版信息

Int J Pept Protein Res. 1979 Apr;13(4):426-33. doi: 10.1111/j.1399-3011.1979.tb01902.x.

DOI:10.1111/j.1399-3011.1979.tb01902.x
PMID:457336
Abstract

[Glu(OMe)4]oxytocin (XVI) and [Mpr1, Glu(OMe)4]oxytocin (XVII) bearing a methyl ester group in place of the carboxamide group in position 4 of oxytocin were synthesized by (3 + 6) segment condensation using the S-trityl group for the protection of the cysteine side chains. Analogue XVI exhibited 10.5 U/mg in vitro uterotonic, and 42 U/mg avian vasodepressor, activity, and analogue XVII 21.4 U/mg and 82 U/mg of the respective activities. Both compounds showed no response in the rat pressor assay.

摘要

相似文献

1
Synthesis and some pharmacological properties of [Glu(OMe)4]oxytocin and [Mpr1, Glu(OMe)4]oxytocin.
Int J Pept Protein Res. 1979 Apr;13(4):426-33. doi: 10.1111/j.1399-3011.1979.tb01902.x.
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Synthesis and some pharmacological properties (4-beta-(2-thienyl)-L-alanine)oxytocin.(4-β-(2-噻吩基)-L-丙氨酸)催产素的合成及一些药理学性质
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J Pept Sci. 2003 Jun;9(6):393-401. doi: 10.1002/psc.471.

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