SYNTHESIS AND SOME PHARMACOLOGICAL PROPERTIES OF 6 NEW ANALOGS OF ARGININE-VASOPRESSIN SUBSTITUTED IN POSITION 2 WITH BETA-THIENYLALANINE OR PROLONGED ON THE N-TERMINUS WITH 1-ADAMANTANEACETIC ACID

被引:1
|
作者
KONIECZNA, E [1 ]
CZAJA, M [1 ]
LAMMEK, B [1 ]
SLANINOVA, J [1 ]
机构
[1] CZECHOSLOVAK ACAD SCI, INST ORGAN CHEM & BIOCHEM, CS-16610 PRAGUE 6, CZECHOSLOVAKIA
关键词
D O I
10.1135/cccc19932994
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Six new analogs of arginine-vasopressin, four of them substituted in position 2 with beta-thienylalanine, and two prolonged on the N-terminus by acylation with I-adamantaneacetic acid, were synthesized on chlormethylated resin using Boc strategy and DCC or DCC-HOBt to form peptide bond. The activity of the analogs was fairly low, however, one of the peptides, namely [Cpp1, Thi2, Val4]AVP, showed selectivity in antiuterotonic, antipressor and anti-antidiuretic effects.
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页码:2994 / 2999
页数:6
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