Sasaki Y, Matsui M, Taguchi M, Suzuki K, Sakurada S, Sato T, Sakurada T, Kisara K
Biochem Biophys Res Commun. 1984 Apr 16;120(1):214-8. doi: 10.1016/0006-291x(84)91435-9.
To examine pharmacological properties of D-Arg2-dermorphin tetrapeptides, six tetrapeptide analogs based on the following formulas, H-Tyr-D-Arg-Phe-Gly-OX (X = H, ethyl, n-propyl), H-Tyr-D-Arg-Phe-Sar-OX (Sar = sarcosine; X = H, methyl, ethyl), were prepared. All these analogs exhibited highly potent and long-lasting analgesia as compared with that of morphine after subcutaneous administration in mice. Among analogs tested, H-Tyr-D-Arg-Phe-Sar-OH showed the highest activities, which were 21, 30 and 58 times more active than morphine in the tail pressure, tail flick and phenylbenzoquinone writhing tests, respectively, on a molar basis.
为研究D-精氨酸2-皮啡肽四肽的药理学特性,制备了六种基于以下化学式的四肽类似物:H-Tyr-D-Arg-Phe-Gly-OX(X = H、乙基、正丙基),H-Tyr-D-Arg-Phe-Sar-OX(Sar = 肌氨酸;X = H、甲基、乙基)。与皮下注射吗啡的小鼠相比,所有这些类似物均表现出高效且持久的镇痛作用。在所测试的类似物中,H-Tyr-D-Arg-Phe-Sar-OH表现出最高的活性,在尾部压力、甩尾和苯醌扭体试验中,以摩尔为基础,其活性分别比吗啡高21倍、30倍和58倍。