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・ Heteroclinus puellarum
・ Heteroclinus roseus
・ Heteroclinus tristis
・ Heteroclinus whiteleggii
・ Heteroclinus wilsoni
・ Heteroclisis
・ Heteroclite
・ Heterocloeon
・ Heteroclytomorpha
・ Heterocnephes
・ Heterocnephes apicipicta
・ Heterocnephes delicata
・ Heterocnephes lymphatalis
・ Heterocnephes scapulalis
・ Heterocnephes vicinalis
Heterocodeine
・ Heterocodon
・ Heterocoma
・ Heterocompsa
・ Heterocompsa aquilonia
・ Heterocompsa eburata
・ Heterocompsa formosa
・ Heterocompsa geniculata
・ Heterocompsa nigripes
・ Heterocompsa seabrai
・ Heterocompsa stellae
・ Heterocompsa truncaticornis
・ Heterocondylus
・ Heteroconger
・ Heteroconger balteatus


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Heterocodeine : ウィキペディア英語版
Heterocodeine

Heterocodeine (6-methoxymorphine) is an opiate derivative, the 6-methyl ether of morphine, and a structural isomer of codeine; it is called "hetero-" because it is the reverse isomer of codeine. Heterocodeine was first synthesised in 1932 and first patented in 1935.〔US Patent 2058521〕 It can be made from morphine by selective methylation.〔Barber RB, Rapoport H. Synthesis of thebaine and oripavine from codeine and morphine. ''Journal of Medicinal Chemistry''. 1975 Nov;18(11):1074-7.〕 Codeine is the natural mono-methyl ether, but must be metabolized for activity (that is, it is a prodrug). In contrast the semi-synthetic mono-methyl ether, heterocodeine is a direct agonist. The 3,6 methyl di-ether of morphine is thebaine.
Heterocodeine is 6 times more potent than morphine〔(Chemistry of Opioid Analgesics - Neurology Pharmacotherapeutics, Wilson and Gisvold, pgs. 629-656. )〕 due to having a substitution at the 6-hydroxy position, in a similar manner to 6-acetylmorphine.〔(Biological evaluation of compounds for their physical dependence potential & abuse liability. XXIV. Drug evaluation committee of the college on problems of drug dependence (2000) A. Coop (Biological Coordinator, DEC, CPDD), & A. E. Jacobson )〕 The drug methyldihydromorphine (dihydroheterocodeine) is a derivative of heterocodeine. Like the morphine metabolite morphine-6-glucuronide, 6-position branches (esters or ethers) of morphine bind to the otherwise unagonized human mu receptor subtype mu-3 (or μ3); as well as the 6-acetylmorphine metabolite of heroin this includes heterocodeine.
The relative strength of heterocodeine to codeine has been published as 50, 72, 81, 88, 93, 96, and 108 x.
It is not mentioned specifically in the Controlled Substances Act 1970 but is a Schedule II controlled substance as an analogue of morphinan or morphine under the morphine structure rules of the Analogues Act; in other countries it is usually controlled as a strong opioid.
Homocodeine is a synonym for pholcodine.
== References ==



抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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