Difference between revisions of "Bremazocine"

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'''Bremazocine''' is a [[kappa-opioid receptor|κ-opioid receptor]] [[agonist]] related to [[pentazocine]]. It has [[potency (pharmacology)|potent]] and long-lasting [[analgesic]] and [[diuretic]] effects.<ref name="pmid16007240">{{cite journal |author=Dortch-Carnes J, Potter DE |title=Bremazocine: a kappa-opioid agonist with potent analgesic and other pharmacologic properties |journal=CNS Drug Reviews |volume=11 |issue=2 |pages=195–212 |year=2005 |pmid=16007240 |doi= |url=}}</ref>
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'''Bremazocine''' is a [[kappa-opioid receptor|κ-opioid receptor]] [[agonist]] related to [[pentazocine]]. It has [[potency (pharmacology)|potent]] and long-lasting [[analgesic]] and [[diuretic]] effects.<ref name="pmid16007240">{{cite journal |author=Dortch-Carnes J, Potter DE |title=Bremazocine: a kappa-opioid agonist with potent analgesic and other pharmacologic properties |journal=CNS Drug Reviews |volume=11 |issue=2 |pages=195–212 |year=2005 |pmid=16007240 |doi= 10.1111/j.1527-3458.2005.tb00270.x|url=}}</ref>
  
 
== See also ==
 
== See also ==

Revision as of 12:34, 20 September 2010

Bremazocine
File:Bremazocine.svg
Systematic (IUPAC) name
6-ethyl- 3-[(1-hydroxycyclopropyl)methyl]- 11,11-dimethyl- 1,2,3,4,5,6-hexahydro- 2,6-methano- 3-benzazocin-8- ol
or
2-(1-hydroxy- cyclopropylmethyl)- 5-ethyl- 9,9-dimethyl- 2'-hydroxy- 6,7-benzomorphan
Clinical data
Routes of
administration		 Oral
Legal status
Legal status
  •  ?
Identifiers
CAS Number 75684-07-0
ATC code none
PubChem CID 1223
IUPHAR/BPS 1603
ChemSpider 1186
Chemical data
Formula C20H29NO2
Molar mass 315.45 g/mol[[Script error: No such module "String".]]
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Bremazocine is a κ-opioid receptor agonist related to pentazocine. It has potent and long-lasting analgesic and diuretic effects.[1]

See also

References

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  1. ↑ Dortch-Carnes J, Potter DE (2005). "Bremazocine: a kappa-opioid agonist with potent analgesic and other pharmacologic properties". CNS Drug Reviews. 11 (2): 195–212. doi:10.1111/j.1527-3458.2005.tb00270.x. PMID 16007240. 
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