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Pharmazie ; 58(5): 300-2, 2003 May.
Article in English | MEDLINE | ID: mdl-12779044

ABSTRACT

Four stereoisomers 1a-d of cis-fluoro-ohmefentanyl have been synthesized. Their absolute configurations were determined by X-ray analysis of (3S,4R,2'S)-(-)-cis-I d. The analgesic activity (mice, sc, hot plate) revealed extreme stereodifferences. The ED50 value of (3R,4S,2'S)-(+)-cis-I (1a) was 0.000774 mg/kg (17958 times more potent than that of morphine), while the corresponding antipode 1c was almost inactive.


Subject(s)
Analgesics, Opioid/chemical synthesis , Analgesics, Opioid/pharmacology , Fentanyl/chemical synthesis , Animals , Chemical Phenomena , Chemistry, Physical , Crystallography, X-Ray , Fentanyl/analogs & derivatives , Fentanyl/pharmacology , Indicators and Reagents , Magnetic Resonance Spectroscopy , Mice , Molecular Conformation , Morphine/pharmacology , Stereoisomerism , Structure-Activity Relationship
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