Synthesis and biological activities of analogs of angiotensins II and III containing O-methyltyrosine and D-tryptophan
作者:John M. Matsoukas、Mahesh H. Goghari、Martin N. Scanlon、Kevin J. Franklin、Graham J. Moore
DOI:10.1021/jm00383a015
日期:1985.6
substitution. Substitution of the Tyr residue in ANG II, but not ANG III, provides a new route for the synthesis of potent and competitive angiotensin antagonists. Differences in the biological properties of ANG II and ANG III analogues substituted at the Tyr residue suggest different binding/conformation requirements for the two endogenous ligands at angiotensin receptors in smooth muscle.
通过固相方法合成了取代酪氨酸和/或苯丙氨酸残基的血管紧张素II和III(ANG II和ANG III)的类似物,并通过(羧甲基)纤维素色谱和反相HPLC进行了纯化。在大鼠分离子宫试验中确定了这些肽的拮抗剂和激动剂效力。[Sar1,Tyr(Me)4] ANG II,[Tyr(Me)3] ANG III,[Sar1,D-Trp4] ANG II,[D-Trp3] ANG III,[Sar1,D-Trp8] ANG II, [D-Trp7] ANG III,[Sar1,Tyr(Me)4,Ile8] ANG II,[Tyr(Me)3,Ile7] ANG III,[Sar1,D-Trp4,Ile8] ANG II,[D-Trp3 ,Ile7] ANG III,[Sar1,Tyr(Me)4,D-Trp8] ANG II和[Tyr(Me)3,D-Trp7] ANG III的拮抗活性(pA2)分别为8.1,小于6。小于6,小于6,(7