Synthesis, antidiuretic and pressor activities of [arginine4]arginine-vasopressin and two related analogues.

P Rekowski, B Lammek, P Melin, U Ragnarsson, G Kupryszewski
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引用次数: 12

Abstract

Using well-established solid-phase techniques, three new analogues of arginine-vasopressin (AVP) were synthesized. In these the glutamine residue in position 4 was replaced with an additional arginine. The new analogues were: [Arginine4]arginine-vasopressin ([Arg4]AVP), [2-thiopropionic acid1,arginine4]arginine-vasopressin (d[Arg4]AVP) and [1-thiocyclohexaneacetic acid1,arginine4]arginine-vasopressin (d(CH2)5[Arg4]AVP). [Arg4]AVP showed about the same antidiuretic activity as AVP but had only about 40% of its pressor activity. Unexpectedly, deamination caused a drop in the antidiuretic activity to about 50%. d(CH2)5[Arg4]AVP had practically negligible antidiuretic and low pressor effects.

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[精氨酸]精氨酸-加压素及两种相关类似物的合成、抗利尿和加压活性。
采用成熟的固相技术,合成了三种新的精氨酸-加压素(AVP)类似物。在这些实验中,位置4的谷氨酰胺残基被额外的精氨酸取代。新的类似物有:[精氨酸4]精氨酸-加压素([Arg4]AVP)、[2-硫丙酸1,精氨酸4]精氨酸-加压素(d[Arg4]AVP)和[1-硫环己基乙酸1,精氨酸4]精氨酸-加压素(d(CH2)5[Arg4]AVP)。[Arg4]AVP表现出与AVP相同的抗利尿活性,但只有其升压活性的40%左右。出乎意料的是,脱氨作用导致抗利尿活性下降约50%。d(CH2)5[Arg4]AVP的抗利尿和降压作用几乎可以忽略不计。
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