肽
兴奋剂
阿片肽
(+)-纳洛酮
化学
氨基酸
止痛药
类阿片
受体
阿片受体
肽合成
药理学
立体化学
生物化学
医学
作者
Colette T. Dooley,NN Chung,Brian C. Wilkes,P. Schiller,J. M. Bidlack,G W Pasternak,R A Houghten
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1994-12-23
卷期号:266 (5193): 2019-2022
被引量:169
标识
DOI:10.1126/science.7801131
摘要
A synthetic combinatorial library containing 52,128,400 D-amino acid hexapeptides was used to identify a ligand for the μ opioid receptor. The peptide, Ac-rfwink-NH 2 , bears no resemblance to any known opioid peptide. Simulations using molecular dynamics, however, showed that three amino acid moieties have the same spatial orientation as the corresponding pharmacophoric groups of the opioid peptide PLO17. Ac-rfwink-NH 2 was shown to be a potent agonist at the μ receptor and induced long-lasting analgesia in mice. Analgesia produced by intraperitoneally administered Ac-rfwink-NH 2 was blocked by intracerebroventricular administration of naloxone, demonstrating that this peptide may cross the blood-brain barrier.
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