Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
July 11, 2007Journal of Medicinal ChemistryOpen Access

Probes for Narcotic Receptor Mediated Phenomena. 34. Synthesis and Structure−Activity Relationships of a Potent μ-Agonist δ-Antagonist and an Exceedingly Potent Antinociceptive in the Enantiomeric C9-Substituted 5-(3-Hydroxyphenyl)-N-phenylethylmorphan Series

View Full Paper
Ask AI
Bookmark
Share

Authors

AHAnne‐Cecile HiebelYLYong Sok LeeEBEdward J. Bilsky

Discussion

Loading...

Member takes

Overview

Key Points

Key points are not available for this paper at this time.

Cite This Study

Hiebel et al. (2007) studied this question.

synapsesocial.com/papers/6a5e919fa2fbe976fe5ff02fhttps://doi.org/10.1021/jm061325e
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Single-File Transport of Water Molecules through a Carbon Nanotube2002 · 402 citations
  2. 2STRUCTURES RELATED TO MORPHINE. IV.1 m-SUBSTITUTED PHENYLCYCLOHEXANE DERIVATIVES1955 · 36 citations
  3. 3Opioid ligands with mixed properties from substituted enantiomeric N -phenethyl-5-phenylmorphans. Synthesis of a µ-agonist δ-antagonist and δ-inverse agonists2007 · 24 citations