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Myricetin is a naturally occurring flavonoid of the flavonol subclass, a plant pigment found in many fruits, vegetables, berries, teas and wines. Closely related in structure to quercetin, it is studied chiefly for antioxidant and anti-inflammatory activity and a broad range of other effects observed in the laboratory. It is not a drug but a dietary compound, consumed in ordinary foods and sold as a supplement.
- Strong antioxidant activity
- Preclinical anti-inflammatory effects
- May support glucose control
- Possible neuroprotective signals
- Could interact with medicines by affecting drug-metabolizing enzymes
Overview
Myricetin is a flavonoid, one of the large family of polyphenolic compounds that give many plants their color and contribute to their chemistry. More precisely it is a flavonol, the same structural subclass as quercetin, to which it is closely related and with which it shares many properties; chemically it is a hexahydroxyflavone, meaning it carries six hydroxyl groups on the flavonoid skeleton, a feature central to its antioxidant behavior [1].
Myricetin is widely distributed in the diet. It occurs in a range of fruits and vegetables, in berries, nuts, tea, red wine and various herbs, so that most people consume small amounts of it regularly, though typical daily intake is modest [1][2]. Because it is a normal constituent of foods, it is generally encountered as part of a mixed diet rather than in isolation, and it is also marketed on its own as a dietary supplement [1].
A large body of laboratory research has examined myricetin's biological activities. It is described as a strong antioxidant that scavenges reactive oxygen species and binds metal ions, and it has shown anti-inflammatory, antiviral, antithrombotic, neuroprotective, antidiabetic and anticancer effects in cell and animal studies [1][3][4]. Reviews highlight its potential relevance to conditions ranging from cardiovascular disease and diabetes to neurodegenerative disorders, and it has been studied for effects on inflammatory enzymes and cell-signaling pathways involved in cancer [3][4]. It is important to note, however, that much of this evidence comes from preclinical work; robust human clinical data are limited, and the compound's low absorption after ingestion is a recognized obstacle to translating laboratory findings into practical use [4].
Myricetin also has a more complicated side: under certain conditions it can behave as a prooxidant, undergoing autoxidation that generates free radicals, and it has produced mixed results in tests of mutagenicity, showing both anti-mutagenic and, in some assays, mutation-promoting behavior [1]. It is not an approved medicine but a dietary flavonoid, treated as a food component and supplement ingredient rather than a pharmaceutical [1].
Mechanism
Myricetin's effects stem largely from its chemistry as a polyphenol rich in hydroxyl groups. These groups let it act as an antioxidant in several ways: it donates electrons to neutralize reactive oxygen species and free radicals, it chelates transition metal ions such as iron and copper that would otherwise catalyze the formation of damaging radicals, and it can induce protective cellular enzymes such as glutathione S-transferase that help defend against [1].
Beyond direct antioxidant action, myricetin interacts with a variety of enzymes and signaling molecules; it inhibits inflammatory enzymes including cyclooxygenase and lipoxygenase, dampens mediators such as inducible synthase and cyclooxygenase-2, modulates cell-signaling pathways linked to cell growth and survival, and can interfere with enzymes such as certain viral reverse transcriptases [1][3][4]. The same reactive chemistry has a double edge: in some settings myricetin autoxidizes and generates superoxide and hydroxyl radicals, acting as a prooxidant, and this pro-oxidative behavior is thought to contribute both to potential cell damage and to some of its anticancer effects [1][4].
receptor fingerprint
Reactive oxygen speciesscavenges
NF-kB signalinginhibits
Alpha-glucosidaseinhibits
Amyloid aggregationmodulates
Dosingtypical ranges, not medical advice
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Safetyrisks and cautions, not medical advice
Dietary myricetin is considered safe. Concentrated supplement doses are less studied; very high intakes could theoretically have pro-oxidant or enzyme-inhibiting effects. Interactions with drug-metabolizing enzymes are possible, so caution with medications.
Subjective profileweighing the evidence above
A potent antioxidant flavonoid with interesting preclinical breadth but weak human evidence; fine to get from diet, modest expectations as a supplement.
Resources
This entry is here for reference.
Research
- 1997first citedBiological effects of myricetin.
- 2023most recentMyricetin: A Significant Emphasis on Its Anticancer Potential via the Modulation of Inflammatio…
- 1.Myricetin: A Dietary Molecule with Diverse Biological Activities.
- 2.Biological effects of myricetin.
- 3.Flavonols and Flavones as Potential anti-Inflammatory, Antioxidant, and Antibacterial Compounds.
- 4.Myricetin: A Significant Emphasis on Its Anticancer Potential via the Modulation of Inflammation and Signal Transduction Pathways.
4 listed here; entry last updated August 2026
Reviews
My notesprivate to this device
FAQ
What foods have myricetin?
Berries, grapes, red wine, tea, and various vegetables and herbs.
Is it proven in humans?
No. Most evidence is from cell and animal studies; human trials are limited.
Why is bioavailability a problem?
Like many flavonoids, it's poorly absorbed and rapidly metabolized, so blood levels stay low.
Can it help blood sugar?
Preclinical work suggests it may blunt glucose spikes, but this isn't established in people.
Any drug interactions?
It can affect drug-metabolizing enzymes in the lab, so be cautious if you take medications.
Limitations of the evidence
- Human safety data for concentrated supplements are limited
Adverse effects
- Could interact with medicines by affecting drug-metabolizing enzymes
Notes and cautions
- Generally regarded as safe at the small amounts present in foods
- May act as a prooxidant at high concentrations
- Poorly absorbed when taken by mouth