Abstract
Several studies have suggested functional association between μ-opioid and δ-opioid receptors and showed that μ-activity could be modulated by δ-ligands. The general conclusion is that agonists for the δ-receptor can enhance the analgesic potency and efficacy of μ-agonists. Our preliminary investigations demonstrate that new bivalent ligands constructed from the μ-agonist fentanyl and the δ-agonist enkephalin-like peptides are promising entities for creation of new analgesics with reduced side effects for treatment of neuropathic pain. A new superposition of the mentioned pharmacophores led to novel μ-bivalent/δ-bivalent compounds that demonstrate both μ-opioid and δ-opioid receptor agonist activity and high efficacy in anti-inflammatory and neuropathic pain models with the potential of reduced unwanted side effects.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 1228-1235 |
| Number of pages | 8 |
| Journal | Journal of Heterocyclic Chemistry |
| Volume | 54 |
| Issue number | 2 |
| DOIs | |
| State | Published - Mar 2017 |
ASJC Scopus subject areas
- Organic Chemistry