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| Myricetin (MYR; 3,3′,4′,5,5′,7-hexahydroxyflavone) is a dietary flavonol polyphenol abundant in berries, tea, red wine, and some medicinal plants. Its dominant biology is redox-active modulation with context-dependent pro-oxidant capacity, ranking conceptually as: (1) ROS modulation (scavenging at low dose; pro-oxidant at higher dose or with metal redox cycling), (2) PI3K/Akt/mTOR and MAPK pathway inhibition, (3) NF-κB suppression and inflammatory signaling control, and (4) mitochondrial apoptosis induction (caspase activation, ΔΨm disruption). Bioavailability is limited by low aqueous solubility and rapid conjugation (glucuronidation/sulfation); reported human plasma levels after dietary exposure are typically sub-micromolar (<1 µM), while many in-vitro cancer studies use 10–100 µM, often exceeding realistic systemic exposure. Clinical evidence remains preclinical-dominant; no robust RCT-grade anticancer efficacy established. Redox duality implies potential chemo-sensitization in oxidative tumors but also theoretical protection of normal tissue. -Possible inhibitory effects on mammalian TrxRs (thioredoxin reductase) Myricetin (MYR) — Cancer-Relevant Pathway Effects
TSF Legend: P: 0–30 min R: 30 min–3 hr G: >3 hr
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| Power to enhance an anti cancer effect |
| 1997- | Myr, | QC, | Inhibition of Mammalian thioredoxin reductase by some flavonoids: implications for myricetin and quercetin anticancer activity |
| - | in-vitro, | Lung, | A549 |
Query results interpretion may depend on "conditions" listed in the research papers. Such Conditions may include : -low or high Dose -format for product, such as nano of lipid formations -different cell line effects -synergies with other products -if effect was for normal or cancerous cells
Filter Conditions: Pro/AntiFlg:% IllCat:% CanType:% Cells:% prod#:127 Target#:961 State#:% Dir#:1
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