Cannabigerovarin (CBGV) Cannabinoid Research

Cannabigerovarin (CBGV) Research Dashboard

2

Primary Studies

2

Related Studies

4

Total Studies

Clinical Studies

0

Clinical Meta-analyses

0

Double-blind Clinical Trials

0

Clinical Trials

Pre-Clinical Studies

0

Meta-analyses/Reviews

0

Animal Studies

2

Laboratory Studies

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CannaKeys has 4 studies associated with Cannabigerovarin (CBGV).

Here is a small sampling of Cannabigerovarin (CBGV) studies by title:


Components of the Cannabigerovarin (CBGV) Research Dashboard

  • Top medical conditions associated with Cannabigerovarin (CBGV)
  • Proven effects in clinical trials for Cannabigerovarin (CBGV)
  • Receptors associated with Cannabigerovarin (CBGV)
  • Individual study details for Cannabigerovarin (CBGV)

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Overview - Cannabigerovarin (CBGV)

Description of Cannabigerovarin (CBGV)

CBGV (Cannabigerovarin) was first isolated and identified in the mid-seventies (Y. Shoyama et al., 1975) who extracted it from a Thai strain (Meao) of Cannabis sativa using chromatographic techniques. This discovery was part of broader research into varin-type cannabinoids, which are characterized by a shorter three-carbon (propyl) side chain, compared to the more common five-carbon (pentyl) side chain found in cannabinoids like CBG. The identification of CBGV contributed to the expanding understanding of the chemical diversity within the cannabis plant and laid the groundwork for subsequent studies into its potential pharmacological properties.


CBGV is the neutral (decarboxylated) form of CBGVA (Cannabigerovarinic acid), which is the acidic precursor produced by the plant. During heating or aging, CBGVA naturally converts into CBGV through decarboxylation—a process similar to how THCA becomes THC or CBDA becomes CBD.


Cannabigerovarin (CBGV) is found in trace amounts in the cannabis plant and is closely related to Cannabigerol (CBG), often called the “mother cannabinoid” because it helps form many other cannabinoids during the plant’s growth.


Like CBG, CBGV is non-intoxicating, meaning it doesn’t cause changes in cognition. Although it’s found in smaller amounts, early research suggests that CBGV may have potential therapeutic benefits, particularly in areas like inflammation, skin health, as a supportive compound in topical formulations, and cancer.

Other Names:

Cannabigerovarin

Cannabigerivarin plus numerous other supplier-based synonyms.


IUPAC Name: 2-[(2E)-3,7-dimethylocta-2,6-dienyl]-5-propylbenzene-1,3-diol


Molecular Formula: C19H28O2


Source–PubChem

Cannabigerovarin (CBGV) Properties and Effects

Only Members can view Properties and Effects information. See DEMO page.

Cannabigerovarin (CBGV) Receptor Binding

Only Members can view Receptor Binding information. See DEMO page.

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Information on this site is provided for informational purposes only and is not meant to substitute for the advice provided by your own licensed physician or other medical professional. You should not use the information contained herein for diagnosing or treating a health problem or disease. If using a product, you should read carefully all product packaging. If you have or suspect that you have a medical problem, promptly contact your health care provider.

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.