5 research outputs found
Discovery and Pharmacological Evaluation of a Diphenethylamine Derivative (HS665), a Highly Potent and Selective κ Opioid Receptor Agonist
Here we report on the design, synthesis, and biological
characterization
of novel κ opioid (KOP) receptor ligands of diphenethylamines.
In opioid receptor binding and functional assays, the <i>N</i>-cyclobutylmethyl substituted derivative <b>4</b> (HS665) showed
the highest affinity and selectivity for the KOP receptor and KOP
agonist potency. Compound <b>4</b> inhibited acetic acid induced
writhing after subcutaneous administration in mice via KOP receptor-mediated
mechanisms, being equipotent as an analgesic to the KOP agonist U50,488
Synthesis and Pharmacological Activities of 6-Glycine Substituted 14-Phenylpropoxymorphinans, a Novel Class of Opioids with High Opioid Receptor Affinities and Antinociceptive Potencies
The synthesis and the effect of a combination of 6-glycine and 14-phenylpropoxy substitutions in <i>N</i>-methyl- and <i>N</i>-cycloproplymethylmorphinans on biological activities are described. Binding studies revealed that all new 14-phenylpropoxymorphinans (<b>11</b>−<b>18</b>) displayed high affinity to opioid receptors. Replacement of the 14-methoxy group with a phenylpropoxy group led to an enhancement in affinity to all three opioid receptor types, with most pronounced increases in δ and κ activities, hence resulting in a loss of μ receptor selectivity. All compounds (<b>11</b>−<b>18</b>) showed potent and long-lasting antinociceptive effects in the tail-flick test in rats after subcutaneous administration. For the <i>N</i>-methyl derivatives <b>13</b> and <b>14</b>, analgesic potencies were in the range of their 14-methoxy analogues <b>9</b> and <b>10</b>, respectively. Even derivatives <b>15</b>−<b>18</b> with an <i>N</i>-cyclopropylmethyl substituent acted as potent antinociceptive agents, being several fold more potent than morphine. Subcutaneous administration of compounds <b>13</b> and <b>14</b> produced significant and prolonged antinociceptive effects mediated through peripheral opioid mechanisms in carrageenan-induced inflammatory hyperalgesia in rats