227-871-1

应用筛选条件

关键词:'227-871-1'

显示 1-1 共 1 条结果关于 "227-871-1" 范围论文

Design of oxytocin antagonists, which are more selective than atosiban.

M Manning et al.

Journal of peptide science : an official publication of the European Peptide Society, 7(9), 449-465 (2001-10-06)

We report the solid phase synthesis of four pairs of L- and D-thienylalanine (Thi/D-Thi) position two modified analogues of the following four oxytocin (OT) antagonists: des-9-glycinamide [1-(beta-mercapto-beta,beta-pentamethylene propionic acid), 2-O-methyltyrosine, 4-threonine]ornithine-vasotocin (desGly(NH2)9,d (CH2)5[Tyr(Me)2,Thr4]OVT) (A); the Tyr-(NH2)9 analogue of (A), d(CH2)5[Tyr(Me)2,Thr4,Tyr-(NH2)9]OVT

1/1