Open Access Articles- Top Results for Hydromorphinol


Systematic (IUPAC) name
Clinical data
2183-56-4 7pxY
PubChem CID 5463858
ChemSpider 4576407 7pxN
UNII 1O00P9X5C1 7pxN
Synonyms Hydromorphinol,
Chemical data
Formula C17H21NO4
303.35 g/mol
 14pxN (what is this?)  (verify)

Hydromorphinol (RAM-320, 14-Hydroxydihydromorphine)[1] is an opiate analogue that is a derivative of morphine, where the 14-position has been hydroxylated and the 7,8- double bond saturated.[2] It has similar effects to morphine such as sedation, analgesia and respiratory depression, but is more potent and has a steeper dose-response curve and longer half-life.[3] It is used in medicine as the bitartrate salt (free base conversion ratio 0.643, molecular weight 471.5) and hydrochloride (free base conversion ratio 0.770, molecular weight 393.9)

Hydromorphinol was developed in Austria in 1932. It is available, and commonly used, as a medicine in Sweden; in the United States, it was never available and is classified as a Schedule I drug with a DEA ACSCN of 9301. The 2013 DEA production quota for hydromorphinol is 54 grammes.

Hydromorphinol is metabolised mainly in the liver in the same fashion as many other opioids and is itself a minor active metabolite of 14-Hydroxydihydrocodeine, an uncommonly-used opiate (but is therefore also an active metabolite of a first-order active metabolite of oxycodone).

It is distributed under the trade name Numorphan in some countries, whereas this trade name is used for oxymorphone much more commonly. It is controlled under the Single Convention On Narcotic Drugs.

See also


  1. ^ US 2960505, Weiss U., published 11/15/1960 
  2. ^ Weiss, U.; Daum, S. J. (1965). "Derivatives of Morphine. Iv. 14-Hydroxymorphine and 14-Hydroxydihydromorphine". Journal of Medical Chemistry 8: 123–125. PMID 14287245. doi:10.1021/jm00325a028.  edit
  3. ^ Plummer, J. L.; Cmielewski, P. L.; Reynolds, G. D.; Gourlay, G. K.; Cherry, D. A. (1990). "Influence of polarity on dose-response relationships of intrathecal opioids in rats". Pain 40 (3): 339–347. PMID 2326098. doi:10.1016/0304-3959(90)91131-2.  edit


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