4.7 Article

Synthesis, Conformation, and Biological Characterization of a Sugar Derivative of Morphine that is a Potent, Long-Lasting, and Nontolerant Antinociceptive

Journal

JOURNAL OF MEDICINAL CHEMISTRY
Volume 52, Issue 9, Pages 2656-2666

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jm8011245

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Funding

  1. Fundacio La Marato de TV3 [070430]
  2. CDTI [391, 96 0175]
  3. Ministry of Education and Science of Spain [CTQ 2006 10874 CO2 01]
  4. EC Marie Curie Research Training Network [MRTN CT 2005 019561]

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A synthetic mannoside derivative, namely, 6-morphinyl-alpha-D-mannopyranoside, shows a naloxone-reversible antinociception that is 100-fold more potent and twice as long lasting compared to morphine when administered intraperitoneally to rats in paw pressure, and tail flick tests. The compound does not produce tolerance and binds to rat mu opioid receptors with twice the affinity of morphine. NMR studies suggest that differences of activity between the derivative and its parent compound M6G might be related to their differing molecular dynamic behavior.

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