Ellagitannin (Tannin) — Hermetica Encyclopedia
Named Bioactive Compounds · Compound

Ellagitannin (Tannin)

Provisional Moderate Scorebotanical

Hermetica Superfood Encyclopedia

Evidence review status: unreviewed

Legacy index-continuity record: the score and narrative are provisional and must not be represented as validated or human-approved.

Review flags: AWAITING_SEMANTIC_VALIDATION

Provisional Summary

Ellagitannins are polyphenolic compounds found in berries and pomegranates that convert to urolithin metabolites in the gut. These metabolites demonstrate anti-inflammatory properties through NF-κB pathway modulation and may support digestive and prostate health.

Screened PMID Records
Reported Benefits
Pending
Synergy Review
At a Glance
CategoryNamed Bioactive Compounds
GroupCompound
Public Score StatusProvisional Moderate
Primary Keywordellagitannin benefits
Ellagitannin close-up macro showing natural texture and detail — rich in antioxidant, anti-inflammatory, antimicrobial
Ellagitannin (Tannin) — botanical close-up

Origin & History

Ellagitannin growing in natural environment — natural habitat
Natural habitat

Ellagitannins are hydrolyzable tannins characterized by hexahydroxydiphenoyl units esterified to glucose cores, found naturally in pomegranates, berries (black raspberries, strawberries), walnuts, and oak-aged wines. They occur primarily in fruits, bark, and leaves, extracted using methanol or ethanol solvents, though clinical products typically use whole food matrices like pomegranate juice or standardized berry extracts.

Ellagitannin-rich foods like pomegranate and Terminalia chebula have been used in Ayurvedic and Persian medicine for centuries for digestive disorders, inflammation, and antimicrobial purposes. Pomegranate juice features prominently in Middle Eastern traditions for gut health, though specific ellagitannin attribution is a modern understanding.Traditional Medicine

Research Narrative (Provisional)

Clinical evidence is limited to small intervention studies, with no large-scale RCTs or meta-analyses identified. Key trials include an IBD study (NCT03000101, n=80) testing pomegranate juice, a Phase I/II prostate cancer trial (PMID: 32112501, n=40) with black raspberry, and a microbiota study (PMID: 26189645, n=20) using pomegranate extract.

Preparation & Dosage

Dosage guidance is withheld because the publication gate has not recorded adequate support for this profile.

Nutritional Profile

Ellagitannins are high-molecular-weight polyphenolic compounds (typically 300–4,000+ Da) belonging to the hydrolyzable tannin subclass. They are not a source of macronutrients (negligible protein, fat, carbohydrate contribution) but serve as bioactive secondary plant metabolites. Key chemical features: esters of hexahydroxydiphenic acid (HHDP) with a glucose core. Major individual ellagitannins include punicalagin (pomegranate, up to ~2,000 mg/L in juice), pedunculagin, casuarictin, sanguiin H-6 (raspberries, ~50–80 mg/100 g fresh weight), lambertianin C (blackberries), and vescalagin/castalagin (oak-aged wines, ~10–50 mg/L). Dietary concentrations vary significantly by source: pomegranate juice provides ~1,500–2,500 mg/L total ellagitannins; strawberries ~20–80 mg/100 g FW; raspberries ~150–300 mg/100 g FW; blackberries ~50–150 mg/100 g FW; walnuts ~60–90 mg/100 g; muscadine grapes ~30–70 mg/100 g FW. Upon hydrolysis in the gut (pH-dependent, enzymatic), ellagitannins release ellagic acid, which is further metabolized by gut microbiota (primarily Gordonibacter urolithinfaciens and Ellagibacter isourolithinifaciens) into urolithins (urolithin A, B, C, D), the principal circulating bioactive metabolites. Bioavailability of intact ellagitannins is extremely low (<1% absorption in the upper GI tract) due to high molecular weight and polarity. Ellagic acid absorption is also limited (~<5%). However, urolithins are well absorbed, reaching plasma concentrations of ~0.5–18 µM (urolithin A glucuronide being the dominant circulating form), with a Tmax of 24–48 hours post-ingestion and elimination half-life of ~17–24 hours. Approximately 40% of the population are 'metabotype A' (producing primarily urolithin A), ~10% are 'metabotype B' (producing urolithins A, B, and isourolithin A), and ~50% produce little to no urolithins ('metabotype 0'). Ellagitannins exhibit strong metal-chelating capacity (particularly Fe²⁺, Cu²⁺), high antioxidant capacity (ORAC values ~2–4× higher than simple phenolics per mole), and notable protein-binding affinity. They contain no significant vitamins or minerals themselves but may influence mineral bioavailability by chelating iron and other divalent cations in the gut lumen, potentially reducing non-heme iron absorption by ~20–50% when consumed concurrently with meals.

Reported Mechanism (Provisional)

Mechanism of Action

Ellagitannins are metabolized by gut bacteria into urolithin A and B, which inhibit nuclear factor-κB (NF-κB) signaling pathways. These urolithin metabolites reduce pro-inflammatory cytokines including TNF-α and IL-6 while modulating immune cell activation. The bioavailability depends on individual gut microbiome composition and ellagitannin-metabolizing bacteria.

Clinical Narrative (Provisional)

A small trial (n=80) testing pomegranate juice in IBD patients showed preliminary benefits for inflammatory bowel disease management, though specific outcomes were not quantified. A Phase I/II dose-escalation study (n=40) with black raspberry demonstrated dose-dependent urolithin metabolite formation, indicating successful conversion of ellagitannins. Current evidence remains preliminary with small sample sizes and limited control groups. Larger randomized controlled trials are needed to establish therapeutic efficacy.

Also Known As

Ellagic acid tanninsHydrolyzable tanninsETHexahydroxydiphenoyl estersPunicalaginCastalaginVescalaginGalloyl-HHDP-glucose

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These statements have not been evaluated by the Food and Drug Administration. This content is for informational purposes only and is not intended to diagnose, treat, cure, or prevent any disease.
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