Chloromorphide
180px | |
Systematic (IUPAC) name | |
---|---|
3-hydroxy- 6α-chloro- 7,8-didehydro- 4,5α-epoxy- 17-methylmorphinan | |
Identifiers | |
ATC code | none |
PubChem | CID 5745724 |
Synonyms | α-Chloromorphide |
Chemical data | |
Formula | C17H18ClNO2 |
Molar mass | 303.78 g/mol[[Script error: No such module "String".]] |
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Chloromorphide (α-Chloromorphide) is an opiate analogue that is a derivative of morphine, where the 6-hydroxy group has been replaced by chlorine. Developed in 1933 in Germany, it has approximately ten times the potency of morphine.[1] It has similar effects to morphine such as sedation, analgesia and respiratory depression.
Chloromorphide is one of a series of opioids known as morphides and codides which are important precursors and intermediates in the synthesis of semi-synthetic opioid analgesic drugs, especially those with additions, substitutions, or other modifications at the 7, 8, and/or 14 position on the morphine carbon skeleton; semisynthetics with changes at other positions can also be made from these compounds. The codeine analogue of chloromorphide is alphachlorcodide (α-chlorocodide), an intermediate in one method of desomorphine sythesis which uses codeine as precursor.
References
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40px | This analgesic-related article is a stub. You can help ssf by expanding it. |
- ↑ Yeh HJC, Wilson RS, Klee WA, Jacobson AE. J Pharm Sci 1976; 65: 902.
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