Journal
FUTURE MEDICINAL CHEMISTRY
Volume 6, Issue 4, Pages 385-412Publisher
FUTURE SCI LTD
DOI: 10.4155/fmc.13.215
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Funding
- NIDA NIH HHS [R01 DA013449, P01 DA006284] Funding Source: Medline
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Fentanyl and its analogs have been mainstays for the treatment of severe to moderate pain for many years. In this review, we outline the structural and corresponding synthetic strategies that have been used to understand the structure-biological activity relationship in fentanyl-related compounds and derivatives and their biological activity profiles. We discuss how changes in the scaffold structure can change biological and pharmacological activities. Finally, recent efforts to design and synthesize novel multivalent ligands that act as mu and delta opioid receptors and NK-1 receptors are discussed.
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