Torres J L, Reig F, Valencia G, Rodríguez R E, García-Antón J M
Biological Organic Chemistry Department, Faculty of Medicine, University of Salamanca, Spain.
Int J Pept Protein Res. 1988 May;31(5):474-80. doi: 10.1111/j.1399-3011.1988.tb00906.x.
Different synthetic strategies have been attempted for the synthesis of a glycosylpeptide resulting from the covalent bonding of a sugar residue to the C-terminal carboxyl group of an enkephalin related pentapeptide. The final structure is: Tyr-D-Met-Gly-Phe-Pro [N1.5-beta-D-glucopyranosyl] amide. The in vitro potency on the GPI test of this analogue was IC50 = 64.0 nM. However, its antinociceptive activity by tail immersion tests, after intraperitoneal administration, was 2000 and 200 times higher than morphine in rats and mice, respectively.
人们尝试了不同的合成策略来合成一种糖基化肽,该糖基化肽由一个糖残基与脑啡肽相关五肽的C末端羧基共价结合而成。最终结构为:酪氨酰-D-蛋氨酰-甘氨酰-苯丙氨酰-脯氨酸[N1.5-β-D-吡喃葡萄糖基]酰胺。该类似物在GPI试验中的体外效价为IC50 = 64.0 nM。然而,经腹腔注射后,通过尾部浸入试验测定,其在大鼠和小鼠中的抗伤害感受活性分别比吗啡高2000倍和200倍。