Ohmefentanyl



Ohmefentanyl
Systematic (IUPAC) name
N-[(3R,4S)-1-[(2S)-2-hydroxy-2-phenyl-ethyl] -3-methyl-4-piperidyl]-N-phenyl-propanamide
Identifiers
CAS number 78995-14-9
ATC code  ?
PubChem 62279
Chemical data
O2 
Mol. mass 366.497 g/mol
SMILES search in eMolecules, PubChem
Pharmacokinetic data
Bioavailability  ?
Metabolism  ?
Half life  ?
Excretion  ?
Therapeutic considerations
Pregnancy cat.

?

Legal status
Routes  ?


Ohmefentanyl (β-hydroxy-3-methylfentanyl) is an extremely potent µ-opioid receptor.

Ohmefentanyl is one of the most potent μ-receptor isomers.[2].

The 4"-fluoro analogue of the 3R,4S,βS isomer of ohmefentanyl is the most powerful analgesic potency approximately 18,000-fold greater than morphine.[3]

 


References

  1. ^ Guo GW, He Y, Jin WQ, Zou Y, Zhu YC, Chi ZQ. "Comparison of physical dependence of ohmefentanyl stereoisomers in mice." Life Sciences. 2000;67(2):113-20. PMID 10901279
  2. ^ Liu ZH, He Y, Jin WQ, Chen XJ, Shen QX, Chi ZQ. "Effect of chronic treatment of ohmefentanyl stereoisomers on cyclic AMP formation in Sf9 insect cells expressing human mu-opioid receptors." Life Sciences. 2004 Apr 30;74(24):3001-8. PMID 15051423
  3. ^ Zou Yong, Wu Hao, Yuan Weifang, Dai Qiyuan, Chen Xinjian, Jin Wenqia, Zhu Youcheng. "Synthesis and analgesic activity of stereoisomers of cis-fluoro-ohmefentanyl." Pharmazie. 58 (2003) 5. PMID 12779044

See also

 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Ohmefentanyl". A list of authors is available in Wikipedia.