Phytol – Terpenes and Cannabinoid Research

Phytol Research Dashboard

29

Primary Studies

2

Related Studies

31

Total Studies

Clinical Studies

0

Clinical Meta-analyses

0

Double-blind Clinical Trials

0

Clinical Trials

Pre-Clinical Studies

2

Meta-analyses/Reviews

15

Animal Studies

12

Laboratory Studies

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CannaKeys has 31 studies associated with Phytol.

Here is a small sampling of Phytol studies by title:


Components of the Phytol Research Dashboard

  • Top medical conditions associated with Phytol
  • Proven effects in clinical trials for Phytol
  • Receptors associated with Phytol
  • Individual study details for Phytol

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Overview - Phytol

What is Phytol?

Phytol is a terpene richly represented in nature as part of the larger molecule chlorophyll, which gives leaves their green color and is essential in photosynthesis. As chlorophyll breaks down, phytol is released. It is estimated that about 30% of chlorophyll is phytol.


It is used in many household products like cosmetics, fragrances, shampoos, soaps, and cleaners.


Phytol may have effects that are anti-inflammatory, antioxidant, anti-convulsant, antimicrobial (Staphylococcus aureus), neuroprotective, anti-parasitical (malaria), antihyperglycemic, anti-obesity, pain-reducing, anxiolytic (anti-anxiety), sedating, and may help destroy some types of cancer cells in vitro (adenocarcinoma, hepatocellular).


Is Phytol safe?


Phytol is a clear, colorless, oily liquid. In concentrated forms, it can cause skin irritation.

Other Names

IUPAC Name: (E,7R,11R)-3,7,11,15-tetramethylhexadec-2-en-1-ol


Source–PubChem

Scent Description

Floral, Jasmine, Jasmine green tea, balsam

Natural Sources

Green tea, jasmine, olive trees, wild lettuce

Cannabis Strains High in Phytol

OG Kush, Harlequin, Cannatonic, Trident

Phytol Properties and Effects

Phytol is associated with the following properties and effects:



  1. Anti-diabetic

    1. Improves glucose tolerance (H. Upadhyay et al., 2022)



  2. Anti-microbial

    1. Anti-parasitical (against Plasmodium berghei) (M. Usman et al., 2022



  3. Anti-obesity (Ji-Yeong An et al., 2018)


Anti-inflammatory and antioxidant (via regulation of NF- κB and AP-1 activation, inhibits levels of IL-1β, IL-4, and TNF- α, neutrophil migration, reduces reactive oxygen species and reactive nitrogen species level by activating antioxidative defense system (Superoxide dismutase and catalase) and restoring Glutathione S-transferase)


Anticonvulsant, anxiolytic, sedative, and neuroprotective properties (via possible activities on GABA receptors, anticholinesterase, butyrylcholinesterase, β-secretase 1 (BACE1), attenuating macromolecular damage, antioxidant activities, and regulating apoptosis-mediated cell death)


Antimicrobial against Staphylococcus aureus and Pseudomonas aeruginosa (via inducing oxidative stress response in P. aeruginosa and damage to the cell membranes with bactericidal activity against S. aureus)


Anti-parasitical against schistosomiasis and Plasmodium berghei (via reducing worm burden, egg laying, suppresses parasitemia, reduces anemia, and oxidative brain damage in test animals infected with Plasmodium berghei)


A potential antihyperglycemic and antiobesity agent may improve oral glucose tolerance and increase brown adipocytes (via PPAR-α and -γ binding)


Pain-reducing (via central and peripheral actions, antioxidant properties)


Anticancer and anti-drug resistance activities. It may help destroy some types of adenocarcinoma, hepatocellular, lung, and skin epidermal cancer cells in vitro and ex-vivo.


It prevents drug resistance in AML models. However, it may also cause selective midzonal hepatocellular necrosis in mice (via apoptosis induction through activation of caspase-9/3 and inhibition of EMT in hepatocellular carcinoma cells, apoptosis in human gastric adenocarcinoma AGS cells through downregulation of Bcl-2, upregulation of Bax, the activation of caspase-9 and -3, PARP cleavage, and depolarization of the mitochondrial membrane, suppresses the P-gp expression via NF-κB inhibition in AML, interactions with β-C, AO-(2) and P may cause induction of apoptosis on A431 and HaCaT cells, antioxidant activities)


Last reviewed by Dr. Abraham Benavides, M.D., 05-27-2022

Phytol Receptor Binding

Endocannabinoid System (ECS) and Phytol:


N/A


Endocannabinoidome (eCBome) and Phytol:



  1. PPAR-α (Increased gene expression) (Ji-Yeong An et al., 2018)

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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.