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AM 281

Known as: AM-281, AM281 cpd 
 
National Institutes of Health

Papers overview

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2013
2013
BackgroundCannabinoid receptors and T-type calcium channels are potential targets for treating pain. Here we report on the design… Expand
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2012
2012
Mu-opioid and CB1-cannabinoid agonists produce analgesia; however, adverse effects limit use of drugs in both classes. Additive… Expand
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2011
2011
Both natural and synthetic cannabinoid receptor (e.g., CB1) agonists such as Δ(9)-THC, WIN 55,212-2 (WIN-2), and HU-210 disrupt… Expand
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2011
2011
  • Caron Dean
  • American journal of physiology. Regulatory…
  • 2011
  • Corpus ID: 33402825
Activation of the sympathetic nervous system is fundamental to the coordinated response to stress or danger. The midbrain… Expand
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2004
2004
The acute effects of cannabinoid drugs on the synthesis of noradrenaline, dopamine, and serotonin (5-HT) were assessed… Expand
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2002
2002
The study was undertaken to explore the effect of CP55,940 ((-)-cis-3-[2-Hydroxy4-(1,1-dimethylheptyl) phenyl]-trans-4-(3… Expand
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2002
2002
The study was undertaken to explore the effect of CP55,940 ((-)-cis-3-[2-hydroxy-4-(1,1-dimethylheptyl)phenyl]-trans-4-(3… Expand
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2001
2001
The effect of CP55,940, a presumed CB1/CB2 cannabinoid receptor agonist, on intracellular free Ca2+ levels ([Ca2+]i) in Madin… Expand
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