HU-x Synthetic Cannabinoids Research Dashboard
Double-blind human trials
Clinical human trials
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To see a full dashboard with study details and filtering, go to our DEMO page.
As a subscriber, you will be able to access dashboard insights including chemotype overviews and dosing summaries for medical conditions and organ system and receptor breakdowns for cannabinoid and terpene searches. Study lists present important guidance including dosing and chemotype information with the ability to drill down to the published material. And all outputs are fully filterable, to help find just the information you need. Stay up-to-date with the science of cannabis and the endocannabinoid system with CannaKeys.
CannaKeys has 116 studies associated with HU-x Synthetic Cannabinoids.
Here is a small sampling of HU-x Synthetic Cannabinoids studies by title:
- The Metabolic Efficacy of a Cannabidiolic Acid (CBDA) Derivative in Treating Diet- and Genetic-Induced Obesity
- Cannabinoids in rheumatology: Friend, foe or a bystander?
- G Protein-Coupled Receptors in Osteoarthritis
- HU308 Mitigates Osteoarthritis by Stimulating Sox9-Related Networks of Carbohydrate Metabolism
- Cannabidiol oxidation product HU-331 is a potential anticancer cannabinoid-quinone: a narrative review
Components of the HU-x Synthetic Cannabinoids Research Dashboard
- Top medical conditions associated with HU-x Synthetic Cannabinoids
- Proven effects in clinical trials for HU-x Synthetic Cannabinoids
- Receptors associated with HU-x Synthetic Cannabinoids
- Individual study details for HU-x Synthetic Cannabinoids
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Members can filter by the following criteria:
- Study Type
- Organ Systems
- Study Result
- Year of Publication
Overview - HU-x Synthetic Cannabinoids
Description of HU-x Synthetic Cannabinoids
The HU-x series are synthetic cannabinoids that carry the initials based on their place of discovery Hebrew University, Israel. For instance, HU-210 was discovered in 1988.
HU Family Synthetic Cannabinoids
HU-x Synthetic Cannabinoids Properties and Effects
Binds with PPAR-? and initiates anti-inflammatory responses.
HU-x Synthetic Cannabinoids Receptor Binding
Very strong affinity at mean Ki at human CB1 ~0.25nM (100 times more potent than THC). Very strong affinity for CB2 with a mean Ki at human CB2 is ~0.40nM (86 times more potent than THC)
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Information on this site is based on scientific studies (human, animal, or in vitro), clinical experience, or traditional usage as cited in each article. The results reported may not necessarily occur in all individuals. For many of the conditions discussed, treatment with prescription or over-the-counter medication is also available. Consult your physician, nutritionally oriented health care practitioner, and/or pharmacist for any health problem and before using any supplements or before making any changes in prescribed medications.