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可待因-7,8-氧化物(可待因环氧化物)作为可待因的一种新代谢产物与多种阿片受体的相互作用。

Interactions of codeine-7,8-oxide (codeine-epoxide), as a new metabolite of codeine, with multiple opiate receptors.

作者信息

Konno F, Sato Y, Togashi K, Takayanagi I, Hirobe M

出版信息

Gen Pharmacol. 1985;16(4):379-81. doi: 10.1016/0306-3623(85)90199-5.

Abstract

Interactions of codeine-epoxide, a new metabolite of codeine, with multiple opiate receptors were studied using radioligand binding assay. The ability of codeine-epoxide to displace [3H]dihydromorphine binding was the most effective among three labeled ligands, that is, [3H]dihydromorphine, [3H]-D-Ala2-D-Leu5-enkephalin and [3H]ethylketocyclazocine, suggesting that codeine-epoxide had a selectively high affinity to mu-receptors, despite the fact the affinities of codeine-epoxide to opiate receptors were slightly less potent than its parent compound, codeine. Since "sodium ratio" and "GTP ratio" on codeine-epoxide binding lay between those of codeine and naloxone, the interaction of codeine-epoxide with opiate receptors may be slightly different from that of codeine.

摘要

使用放射性配体结合试验研究了可待因的新代谢产物可待因环氧化物与多种阿片受体的相互作用。在三种标记配体,即[³H]二氢吗啡、[³H]-D-丙氨酸²-D-亮氨酸⁵-脑啡肽和[³H]乙基酮环唑辛中,可待因环氧化物取代[³H]二氢吗啡结合的能力最为有效,这表明可待因环氧化物对μ-受体具有选择性高亲和力,尽管可待因环氧化物对阿片受体的亲和力略低于其母体化合物可待因。由于可待因环氧化物结合的“钠比率”和“GTP比率”介于可待因和纳洛酮之间,可待因环氧化物与阿片受体的相互作用可能与可待因略有不同。

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