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Diacetyldihydromorphine
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Diacetyldihydromorphine
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| Systematic (IUPAC) name |
| (5α,6α)-7,8-Dihydro-4,5-epoxy-17-methylmorphinan-3,6-diacetate |
| Identifiers |
| CAS number |
509-71-7 |
| ATC code |
? |
| PubChem |
5359460 |
| Chemical data |
| Formula |
C21H25NO5 |
| Mol. mass |
371.427 g/mol |
| Synonyms |
Diacetyldihydromorphine, Paralaudin, Dihydroheroin |
| Pharmacokinetic data |
| Bioavailability |
? |
| Metabolism |
? |
| Half life |
? |
| Excretion |
? |
| Therapeutic considerations |
| Pregnancy cat. |
?
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| Legal status |
Schedule I(US)
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| Routes |
Intravenous |
Diacetyldihydromorphine (Paralaudin, Dihydroheroin) is a potent opiate derivative developed in Germany in 1929 which is rarely used in some countries for the treatment of severe pain such as that caused by terminal cancer, as a more potent form of diamorphine (Heroin). Paralaudin is fast acting and longer lasting than diamorphine (heroin), with a duration of action of around 4-7 hours.
Diacetyldihydromorphine is quickly metabolised by plasma esterase enzymes into dihydromorphine, in the same way that diacetylmorphine (heroin) is metabolised into morphine; however unlike dihydromorphine, which is more potent than morphine as an analgesic, diacetyldihydromorphine is actually less potent than diamorphine, perhaps because it is metabolised more slowly. Diacetyldihydromorphine is approximately equipotent to morphine whereas diamorphine is twice the potency of morphine.[1] It shares with other opioids the risk of overdose or (potentially life-threatening) respiratory depression. When strong opioids are required it is more common to use better known drugs such as nicomorphine, oxymorphone or fentanyl which doctors will be more familiar with, and which do not share the stigma associated with heroin. Side effects are similar to those of other opiates and include itching, nausea and constipation.
References
- ^ http://jpet.aspetjournals.org/cgi/content/abstract/133/3/388
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Opioids |
| Opiate derivatives |
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| Morphinans |
Butorphanol • Cyclorphan • Dextro-3-hydroxy-N-allylmorphinan • Dextrorphan • Drotebanol • Levargorphan • Levallorphan • Levorphanol • Levorphan • Levophenacylmorphan • Levomethorphan • Norlevorphanol • Oxilorphan • Phenomorphan • Racemethorphan • Racemorphan
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| Benzomorphans |
Bremazocine • Cyclazocine • Dezocine • Ethylketocyclazocine • Ketazocine • Metazocine • Pentazocine • Phenazocine
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| 4-Phenylpiperidines |
| Pethidines (Meperidines) |
Anileridine • Benzethidine • Carperidine • Difenoxin • Diphenoxylate • Etoxeridine (Carbetidine) • Furethidine • Hydroxypethidine (Bemidone) • Morpheridine • Oxpheneridine (Carbamethidine) • Pethidine (Meperidine) • Pethidine Intermediate A • Pethidine Intermediate B (Norpethidine) • Pethidine Intermediate C (Pethidinic Acid) • Pheneridine • Phenoperidine • Piminodine • Properidine (Ipropethidine) • Sameridine • WIN-7681
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| Prodines |
Allylprodine • α-meprodine • α-prodine • β-meprodine • β-prodine • Meprodine • MPPP • PEPAP • Prodine • Prosidol • Trimeperidine
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| Ketobemidones |
Acetoxyketobemidone • Ketobemidone • Methylketobemidone • Propylketobemidone
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| Others |
Alvimopan • Loperamide • Picenadol |
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| Open Chain Opioids |
| Amidones |
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| Methadols |
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| Moramides |
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| Thiambutenes |
Diethylthiambutene • Dimethylthiambutene • Ethylmethylthiambutene
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| Phenalkoxams |
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| Ampromides |
Diampromide • Phenampromide • Propiram
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| Others |
Lefetamine |
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| Anilidopiperidines |
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| Oripavine derivatives |
7-PET • Acetorphine • Alletorphine • Buprenorphine • Cyprenorphine • Dihydroetorphine • Diprenorphine • Etorphine • N-cyclopropyl-methylnoretorphine
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| Phenazepines |
Ethoheptazine • Meptazinol • Metheptazine • Metethoheptazine • Proheptazine
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| Pirinitramides |
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| Benzimidazoles |
Clonitazene • Etonitazene
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| Others |
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This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Diacetyldihydromorphine". A list of authors is available in Wikipedia.
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