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Conformationally constrained opioid peptide analogs with novel activity profiles
Authors:Peter W Schiller  Ralf Schmidt  Grazyna Weltrowska  Irena Berezowska  Thi M-D Nguyen  Sébastien Dupuis  Nga N Chung  Carole Lemieux  Brian C Wilkes and Katharine A Carpenter
Institution:(1) Laboratory of Chemical Biology and Peptide Research, Clinical Research Institute of Montreal, 110 Pine Avenue West, Montreal, Quebec, Canada, H2W 1R7
Abstract:Novel conformationally constrained opioid peptide analogs with delta antagonist, mixed mgr agonist/delta antagonist or delta agonist properties were developed. TIP(P)-related delta antagonists showed unprecedented delta antagonist potency and delta receptor selectivity, and may have potential for use in analgesia in combination with mgr agonists. A definitive model of their delta receptor-bound conformation was developed. Three prototype mixed mgr agonist/delta antagonists were discovered. They represent the only known compounds with this pharmacological profile and, as expected, one of them was shown to be a potent analgesic and to produce no dependence and less tolerance than morphine. Novel dipeptide derivatives turned out to be potent and selective delta agonists. Because of their low molecular weight and lipophilic character, these compounds may cross the blood-brain barrier and, thus, may have potential as centrally acting analgesics.
Keywords:conformational restriction  delta opioid agonists" target="_blank">gif" alt="delta" align="BASELINE" BORDER="0"> opioid agonists  delta opioid antagonists" target="_blank">gif" alt="delta" align="BASELINE" BORDER="0"> opioid antagonists  mixed mgr opioid agonist/gif" alt="mgr" align="MIDDLE" BORDER="0"> opioid agonist/delta opioid antagonists" target="_blank">gif" alt="delta" align="BASELINE" BORDER="0"> opioid antagonists  opioid peptides  receptor-bound conformation
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