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Eur J Pharm Sci. 2011 Jan 18;42(1-2):65-72. doi: 10.1016/j.ejps.2010.10.007. Epub 2010 Oct 27.

Sulfate esters of morphine derivatives: synthesis and characterization.

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1
Department of Pharmaceutical Chemistry, Semmelweis University, Hőgyes Endre u. 9, Budapest, Hungary. varadian@gytk.sote.hu

Abstract

Sixteen 3-O- and 6-O-sulfate esters of morphine, codeine and some of their N-methyl quaternary derivatives were synthesized by means of sulfation with pyridine-SO(3) complex and sulfuric acid/N,N'-dicyclohexylcarbodiimide. Complete (1)H- and (13)C-NMR assignments are given for each of the synthesized compounds based on one- and two-dimensional homo- and heteronuclear measurements. Comparative analysis of chiral properties by circular dichroism and optical rotatory dispersion revealed characteristic differences in the spectra due to changes in charge, polarity and intramolecular association by strong hydrogen bonds in aqueous solution. The synthesized sulfate esters are prospective peripheral analgesics lacking central side effects and are also useful as reference substances for various analytical studies involving sulfate ester metabolites.

PMID:
21034820
DOI:
10.1016/j.ejps.2010.10.007
[Indexed for MEDLINE]
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