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Theaflavins

Theaflavins

Theaflavins is a water-soluble tea pigment formed during the fermentation of black tea through the condensation of catechins catalyzed by polyphenol oxidase.

Botanical OriginCamellia sinensis (L.) Kuntze

BrandTEATURN®

Spc.TF20,TF40,TF60

CertificationFood Additives (TEATURN Declaration)

Theaflavin (TF) is a water-soluble tea pigment formed during the fermentation of black tea through the condensation of catechins catalyzed by polyphenol oxidase. It consists of four major monomers: theaflavin (TF), theaflavin-3-galactoside (TF-3-G), theaflavin-3'-galactoside (TF-3'-G), and theaflavin-3,3'-di-galactoside (TFDG), accounting for 0.5%–3% of the dry weight of black tea. It is hailed as the "soft gold of tea."

 「The following provides an overview of the therapeutic effects of theaflavins, with descriptions of their functional activities sourced from the literature cited on this website.」

 Powerful antioxidant properties that delay aging

Its radical scavenging efficiency surpasses that of vitamin E (50-fold) and vitamin C (30–50-fold). It directly quenches reactive oxygen species (ROS), chelates metal ions, inhibits lipid peroxidation, and protects cell membranes and DNA from oxidative damage. The compound activates endogenous antioxidant systems such as superoxide dismutase (SOD) and glutathione, reduces markers of oxidative stress (e.g., malondialdehyde, MDA), and delays cellular and systemic aging.

 Regulate blood lipids and protect cardiovascular and cerebrovascular health

Inhibits hepatic HMG-CoA reductase (a key enzyme in cholesterol synthesis), reducing cholesterol production; simultaneously binds bile acids in the intestine and promotes their excretion, thereby achieving dual reductions in total cholesterol and "bad cholesterol" (LDL-C). Clinical studies demonstrate that continuous 12-week administration results in a 16.4% decrease in LDL-C and an 11.3% reduction in total cholesterol, without hepatotoxicity. It protects vascular endothelium, enhances the bioavailability of nitric oxide (NO), dilates blood vessels, reduces blood viscosity, inhibits platelet aggregation and foam cell formation, and delays the progression of atherosclerosis.

 Anti-inflammatory and Immune Regulation

Inhibit inflammatory pathways such as NF-κB and PI3K/Akt, downregulate the expression of pro-inflammatory factors including TNF-α, IL-1β, and IL-6, thereby mitigating chronic inflammatory damage. Regulate the structure of gut microbiota, enhance the intestinal immune barrier, improve immune cell activity, and boost the body's resistance to pathogens.

 Antitumor and Synergistic Chemotherapy

Induces apoptosis of cancer cells (e.g., by activating the Bax/Caspase pathway) and inhibits proliferation and metastasis (e.g., by blocking STAT3 and EGFR signaling), demonstrating inhibitory effects on various tumor cells including hepatocellular carcinoma, breast cancer, and colorectal cancer. When combined with chemotherapeutic agents, it reduces drug resistance, mitigates toxic side effects on normal cells, and enhances therapeutic efficacy.

 

Regulate metabolism and improve glucose and lipid abnormalities

Inhibits α-glucosidase activity, delaying postprandial blood glucose elevation; improves insulin resistance and enhances insulin sensitivity, making it suitable for intervention in type 2 prediabetes. Inhibits fatty acid synthetase (FAS) and lipid absorption, reducing fat accumulation and aiding in weight and body fat percentage control.

 Antibacterial and antiviral properties, safeguarding mucosal health

It exhibits broad-spectrum inhibition against Gram-positive/negative bacteria (e.g., Helicobacter pylori, Streptococcus mutans), disrupting bacterial cell membrane integrity and reducing the risk of dental plaque formation and caries. It inhibits enveloped viruses such as influenza virus, SARS-CoV-2, and HIV by blocking the binding of viral spike proteins to receptors and suppressing key viral replication enzymes (e.g., 3CL protease, RdRP).



  • [1] Liu C W, Zhang Z Y, Wang J Y, et al. Research progress on the biological activities of theaflavins [J]. Food Science, 2022, 43 (19): 38-50. (茶黄素生物学活性研究进展,系统综述抗氧化、抗炎、抗肿瘤等多效性机制)

    [2] Zhang R, Zhang Y H, Zhou J P. Bioactivity, mechanism, and application of theaflavins: a review [J]. Science and Technology of Food Industry, 2025, 46 (10): 1-10. doi: 10.13386/j.issn1002-0306.2024060192. (全面梳理茶黄素在心脑血管、代谢疾病、抗病毒等领域的最新研究与应用前景)

    [3] Mhatre S, D'Souza S, Mhatre S. In silico analysis of theaflavins as potential inhibitors of SARS-CoV-2 3CLpro [J]. Journal of Biomolecular Structure & Dynamics, 2021, 39 (17): 6210-6218. (分子对接证实茶黄素可抑制新冠病毒 3CL 蛋白酶,为抗 COVID-19 提供理论依据)

    [4] Kudo T, Nakamura T, Ohinata H, et al. Effects of oral theaflavin administration on body composition in healthy humans: a randomized, double-blind, placebo-controlled trial [J]. Journal of Nutrition Science, 2020, 9: e10. (随机对照试验证明茶黄素可改善健康人群体脂率、提升骨骼肌占比)

    [5] Wang J, Jiang J J, Zhao C Y, et al. The protective effect of theaflavins on the kidney of mice with Type 2 diabetes mellitus [J]. Nutrients, 2022, 14 (15): 3102. (阐明茶黄素通过抑制 AGEs/MAPK/NF-κB 通路改善糖尿病肾病的机制)

    [6] Sato T, Tanaka T, Sato M. Antibacterial mechanism of theaflavin against Bacillus coagulans [J]. Food Control, 2019, 101: 215-220. (揭示茶黄素通过改变细胞膜磷脂酰甘油亲和力发挥抑菌作用的分子机制)

    [7] Anandhan A, Thennarasu K, Guha M, et al. Theaflavin-3,3'-digallate attenuates neuroinflammation and dopaminergic neurodegeneration in a mouse model of Parkinson's disease [J]. Neuropharmacology, 2020, 168: 107965. (证实茶黄素可抑制神经炎症、保护多巴胺能神经元,为帕金森病干预提供新方向)

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