Yamashiro D, Nicolas P, Li C H
Int J Pept Protein Res. 1983 Mar;21(3):219-22. doi: 10.1111/j.1399-3011.1983.tb03097.x.
Dermorphin (I) and [D-Ala2, Phe3, Gly4, Tyr5, Pro6]-beta c-EP (II) have been synthesized by the solid-phase method (beta c-EP, camel beta-endorphin). Positions 1 through 7 of II correspond to the sequence of I. Relative potencies of synthetic peptides in the mouse tail-flick test for analgesia by the intracerebroventricular route were: human beta-endorphin, 100; camel beta-endorphin, 164; I, 450; II, 440. The dermorphin was about 670 times more potent than morphine in the assay. Peptide II represents a rare instance where the enkephalin moiety of beta-endorphin has been altered to produce a more potent analgesic.
通过固相法合成了皮啡肽(I)和[D-丙氨酸²,苯丙氨酸³,甘氨酸⁴,酪氨酸⁵,脯氨酸⁶]-βc-内啡肽(II)(βc-内啡肽,骆驼β-内啡肽)。II的第1至7位对应于I的序列。通过脑室内途径进行小鼠甩尾镇痛试验时,合成肽的相对效价为:人β-内啡肽,100;骆驼β-内啡肽,164;I,450;II,440。在该测定中,皮啡肽的效力比吗啡高约670倍。肽II代表了一种罕见的情况,即β-内啡肽的脑啡肽部分被改变以产生更强效的镇痛药。