Product Overview

Dihydromyricetin (DHM, INCI: Dihydromyricetin / Ampelopsin, CAS 27200-12-0, C₁₅H₁₂O₈, MW 320.25 g/mol) is a naturally occurring flavanonol — the primary bioactive flavonoid in Ampelopsis grossedentata (vine tea / 藤茶 / rattan tea), a traditional Chinese medicinal herbal tea with centuries of safe consumption history in southern China. DHM's most distinctive and commercially significant pharmacological feature is its action as a GABA-A receptor positive allosteric modulator: it binds at the benzodiazepine site with demonstrated preference for α4β3δ subunit-containing extrasynaptic receptors, enhancing GABA binding affinity and directly counteracting ethanol's excitatory effects on the central nervous system — this is the mechanism underlying DHM's well-documented ability to reverse alcohol intoxication, reduce blood alcohol concentration (BAC), and alleviate hangover symptoms. Simultaneously, DHM enhances alcohol metabolism by upregulating alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH) activity while inhibiting ethanol-induced CYP2E1 — a dual pharmacokinetic/pharmacodynamic approach that accelerates ethanol clearance and reduces toxic acetaldehyde accumulation, providing hepatoprotection confirmed by significant reductions in serum ALT and AST levels. Beyond alcohol-related applications, DHM is a potent AMPK activator and mTOR inhibitor that engages the same longevity and metabolic health pathways as berberine and resveratrol, yet binds at distinct allosteric sites — promoting cellular autophagy, mitochondrial biogenesis, and healthy aging. Structurally, DHM possesses 8 phenolic hydroxyl (-OH) groups in its flavanonol skeleton, which confer exceptional antioxidant capacity with a DPPH IC50 of approximately 6 μg/mL — performance comparable to quercetin — along with anti-inflammatory activity through dual NF-κB pathway and NLRP3 inflammasome inhibition. DHM also demonstrates anti-obesity effects via PPARγ downregulation, inhibiting adipogenesis and lipid accumulation in adipocytes.

As a leading DHM manufacturer and bulk supplier, UPOR Biotech provides high-purity Dihydromyricetin (≥98% HPLC) from Ampelopsis grossedentata leaf extract for the rapidly growing global hangover and alcohol support supplement market, alongside anti-aging, liver health, and metabolic wellness nutraceutical categories. Our DHM is standardized to ≥98% by HPLC with full documentation, batch-to-batch consistency, and competitive bulk pricing — serving B2B supplement brands, nutraceutical formulators, functional beverage manufacturers, and private-label companies worldwide. As a natural flavonoid with a unique GABA-A modulatory mechanism unmatched by any other commercially available flavonoid, and backed by centuries of traditional consumption as vine tea (藤茶), DHM offers compelling market differentiation for products targeting the alcohol support, liver detox, and longevity segments. OEM and private label formulations available with flexible MOQ starting at 1 kg. Free sample available for qualified buyers. Every shipment includes full documentation: COA, MSDS, HPLC chromatogram, and stability data.

DHM vs Quercetin vs Berberine — The Multi-Target Flavonoid Comparison: Why DHM Is the Only GABA-A Modulating Flavonoid with AMPK + mTOR Dual Regulation

Comparing three prominent multi-target flavonoids reveals DHM's unique and complementary positioning. Quercetin is a broad-spectrum flavonoid antioxidant with strong radical scavenging (DPPH IC50 ~7 μg/mL) and anti-inflammatory activity via NF-κB inhibition, but lacks GABA-A receptor modulation entirely and has limited oral bioavailability unless formulated with enhancement technologies — it cannot address alcohol-related applications. Resveratrol is a stilbenoid that activates SIRT1 and AMPK — the canonical longevity pathway — yet provides no alcohol interaction benefit and requires high oral doses (250–500 mg) for clinical effects due to rapid phase II glucuronidation and sulfation metabolism. Berberine is an isoquinoline alkaloid (not a flavonoid) with potent AMPK activation and mTOR inhibition for metabolic health — blood glucose and lipid regulation — but has very poor oral bioavailability (<5%) requiring specialized delivery systems for meaningful systemic exposure. Dihydromyricetin (DHM) is uniquely positioned as the only flavonoid that combines all three therapeutic axes in a single natural molecule: (1) GABA-A receptor positive allosteric modulation at the benzodiazepine site — directly reversing alcohol intoxication and hangover symptoms via α4β3δ subunit-preferring extrasynaptic receptors — a mechanism no other flavonoid provides; (2) AMPK activation + mTOR inhibition via a distinct binding site — engaging longevity and metabolic health pathways parallel to berberine and resveratrol; and (3) potent antioxidant capacity from 8 phenolic -OH groups (DPPH IC50 ~6 μg/mL, comparable to quercetin) with dual NF-κB and NLRP3 inflammasome anti-inflammatory activity. DHM is not a replacement for quercetin, resveratrol, or berberine — it is a complementary multi-target flavonoid that addresses therapeutic gaps the others cannot fill, particularly alcohol-related, GABA-A-mediated, and hangover-reversal applications, all derived from a natural botanical source with centuries of traditional consumption safety data.

Technical Specifications

PropertySpecification
Product NameDihydromyricetin (DHM) Powder — ≥98% HPLC from Vine Tea Extract (Ampelopsis grossedentata)
INCI NameDihydromyricetin (Ampelopsin)
Common Name / SynonymsAmpelopsin; DHM; (+)-Dihydromyricetin; (2R,3R)-3,5,7-Trihydroxy-2-(3,4,5-trihydroxyphenyl)chroman-4-one; Vine Tea Extract; Ampelopsis grossedentata extract; Rattan Tea Extract
CAS Number27200-12-0
Molecular FormulaC₁₅H₁₂O₈
Molecular Weight320.25 g/mol
SourceAmpelopsis grossedentata (vine tea / 藤茶 / rattan tea) leaf extract — natural flavonoid from traditional Chinese medicinal herbal tea
Key AdvantageMulti-target flavonoid: GABA-A receptor positive allosteric modulator (alcohol intoxication reversal at benzodiazepine site) + AMPK activator + mTOR inhibitor + potent antioxidant (8 phenolic -OH groups, DPPH IC50 ~6 μg/mL) + hepatoprotective + anti-inflammatory (NF-κB + NLRP3)
AppearancePale yellow to off-white powder
Assay (Cosmetic/Nutraceutical Grade)≥98% Dihydromyricetin by HPLC (anhydrous basis)
Assay (Standard Grade)≥95% Dihydromyricetin by HPLC (anhydrous basis)
IdentificationHPLC/UV λmax ~292 nm; retention time matches DHM reference standard; IR spectrum conforms to reference
Loss on Drying≤5.0% (105°C, 2 hours)
Residue on Ignition≤0.5%
Melting Point245–247°C (decomposition)
Specific Optical Rotation[α]ᴅ²⁰ +12° to +16° (c=1.0, methanol)
pH (1% Suspension in Water)4.0 – 6.0
SolubilitySoluble in ethanol, methanol, DMSO, and alkaline aqueous solutions; slightly soluble in neutral water; practically insoluble in non-polar organic solvents
Flavonoid ProfileDihydromyricetin (primary, ≥98%), with minor myricetin, dihydroquercetin (taxifolin), and related Ampelopsis flavonoids
Dihydromyricetin Content≥98.0% (anhydrous basis, HPLC at 292 nm)
Heavy Metals (Total)≤10 ppm (as Pb)
Elemental ImpuritiesPb ≤2 ppm; As ≤1 ppm; Hg ≤1 ppm; Cd ≤1 ppm (ICH Q3D compliant)
Microbial LimitsTAMC ≤1,000 CFU/g; TYMC ≤100 CFU/g; Pathogens (E. coli, Salmonella, S. aureus, P. aeruginosa) — Absent in 10 g
Residual SolventsICH Q3C Class 3 compliant
Recommended Dosage300–600 mg for alcohol support (30–60 min before or during alcohol consumption); 100–300 mg daily for general health, antioxidant, and metabolic wellness
Grade / Standards≥98% HPLC (Cosmetic/Nutraceutical Grade); ≥95% HPLC (Standard Grade)
CertificationsISO 9001:2015, ISO 22000, HACCP, FDA Facility Registration, HALAL, KOSHER, Non-GMO, BSE/TSE-Free
Packaging1 kg / 5 kg sealed aluminum foil bags with PE liner; 25 kg fiber drums with double PE liner
Storage15–25°C, tightly sealed in original container, protect from light and moisture
Shelf Life2 years from date of manufacture under recommended storage conditions

Key Benefits — Dihydromyricetin (DHM)

GABA-A Receptor Positive Allosteric Modulation — Alcohol Intoxication Reversal

DHM is the only flavonoid GABA-A receptor positive allosteric modulator — binding at the benzodiazepine site with α4β3δ subunit preference. Directly counteracts ethanol's CNS effects, reduces blood alcohol concentration, accelerates sobriety recovery, and alleviates hangover symptoms (headache, nausea, cognitive impairment). Unique mechanism unmatched by any other natural compound.

GABA-A Modulator

AMPK Activator + mTOR Inhibitor — Longevity & Metabolic Health Pathways

DHM activates AMP-activated protein kinase (AMPK) and inhibits mechanistic target of rapamycin (mTOR) — the same longevity and metabolic health pathways as berberine and resveratrol, but binding at distinct allosteric sites. Promotes cellular autophagy, mitochondrial biogenesis, and healthy aging. Also inhibits adipogenesis via PPARγ downregulation for anti-obesity support.

AMPK + mTOR Dual Regulation

Potent Antioxidant — 8 Phenolic -OH Groups with DPPH IC50 ~6 μg/mL

DHM's flavanonol skeleton contains 8 phenolic hydroxyl (-OH) groups — the structural basis for its exceptional free radical scavenging capacity (DPPH IC50 ~6 μg/mL, comparable to quercetin). One of the most potent natural flavonoid antioxidants available commercially. Protects against oxidative stress across multiple tissue systems.

8 Phenolic -OH Groups

Hepatoprotective + Anti-Inflammatory — Dual NF-κB & NLRP3 Inhibition

DHM significantly reduces serum ALT and AST levels, inhibits ethanol-induced CYP2E1 expression, and protects hepatocytes from alcohol and chemical injury. Anti-inflammatory activity through dual NF-κB pathway and NLRP3 inflammasome inhibition — addressing both acute and chronic inflammatory signaling cascades. Centuries of safe traditional consumption as vine tea (藤茶).

Hepatoprotective

Applications

Hangover Prevention & Alcohol Support Supplements

DHM at 300–600 mg in hangover prevention capsules, alcohol recovery shots, and pre-drinking support formulas — the only natural GABA-A modulating flavonoid that directly reverses alcohol intoxication and accelerates ethanol metabolism. The fastest-growing segment in the global functional supplement market. OEM and private label formulations available.

Liver Detox & Hepatoprotective Nutraceuticals

DHM at 100–300 mg in liver health, detox, and hepatoprotective supplement formulations — reduces ALT/AST, inhibits CYP2E1, and protects against alcohol-induced and chemical liver injury. Complements milk thistle (silymarin) and N-acetylcysteine (NAC) for comprehensive liver support stacks.

Anti-Aging & Longevity Supplement Formulations

DHM as an AMPK activator and mTOR inhibitor in anti-aging, cellular health, and longevity nutraceutical products — engaging the same pathways as berberine and resveratrol with a distinct binding site and natural flavonoid safety profile. Supports autophagy and mitochondrial biogenesis.

Metabolic Health & Weight Management Products

DHM at 100–300 mg in metabolic wellness, healthy weight management, and glucose support supplements — inhibits adipogenesis via PPARγ downregulation and activates AMPK for improved metabolic parameters. Natural botanical positioning with TCM heritage.

Natural Antioxidant & Anti-Inflammatory Formulations

DHM with 8 phenolic -OH groups (DPPH IC50 ~6 μg/mL) in premium antioxidant complexes, anti-inflammatory supplements, and wellness formulations — dual NF-κB and NLRP3 inflammasome inhibition. Comparable antioxidant capacity to quercetin with complementary GABA-A and AMPK mechanisms.

Functional Beverages & Herbal Tea Blend Ingredients

DHM as a functional beverage ingredient — vine tea (藤茶) extract for ready-to-drink herbal teas, wellness shots, botanical powder blends, and functional drink mixes. Natural flavonoid positioning with centuries of traditional consumption heritage in Chinese herbal tea culture.

Frequently Asked Questions

Dihydromyricetin (DHM, CAS 27200-12-0, also known as Ampelopsin) is a natural flavanonol — the primary bioactive flavonoid extracted from the leaves of Ampelopsis grossedentata (vine tea / 藤茶), a traditional Chinese medicinal herbal tea consumed for centuries in southern China. DHM is the only known flavonoid that acts as a GABA-A receptor positive allosteric modulator — it binds at the benzodiazepine site of the GABA-A receptor with preference for α4β3δ subunit-containing extrasynaptic receptors, enhancing GABA binding affinity and directly counteracting ethanol's excitatory effects on the central nervous system. This mechanism directly reverses alcohol intoxication: DHM reduces blood alcohol concentration (BAC), accelerates sobriety recovery, and significantly diminishes hangover symptoms including headache, nausea, and cognitive impairment. DHM simultaneously enhances alcohol metabolism by upregulating alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH) activity while inhibiting ethanol-induced CYP2E1 expression — a dual pharmacokinetic/pharmacodynamic mechanism that accelerates ethanol clearance and reduces toxic acetaldehyde accumulation. UPOR Biotech provides DHM standardized to ≥98% by HPLC from Ampelopsis grossedentata leaf extract, with full COA, MSDS, and HPLC chromatogram documentation.

DHM delivers five clinically and mechanistically validated benefits: (1) Hepatoprotective — DHM significantly reduces serum ALT and AST levels, inhibits ethanol-induced CYP2E1 expression, and protects against both alcohol-induced and chemical liver injury through antioxidant and anti-apoptotic mechanisms in hepatocytes. (2) AMPK activation + mTOR inhibition — DHM activates AMP-activated protein kinase (AMPK) and inhibits mechanistic target of rapamycin (mTOR), engaging the same longevity and metabolic health pathways as berberine and resveratrol but binding at distinct allosteric sites, promoting cellular autophagy, mitochondrial biogenesis, and healthy aging. (3) Anti-obesity and metabolic regulation — DHM inhibits adipogenesis via PPARγ downregulation and suppresses lipid accumulation in adipocytes, supporting healthy body weight and metabolic parameters. (4) Potent antioxidant activity — with 8 phenolic hydroxyl (-OH) groups in its flavanonol structure, DHM demonstrates exceptional free radical scavenging capacity with a DPPH IC50 of approximately 6 μg/mL, comparable to quercetin and superior to most common flavonoids. (5) Anti-inflammatory — DHM inhibits both the NF-κB signaling pathway and NLRP3 inflammasome activation, providing dual-pathway anti-inflammatory protection relevant to chronic inflammatory conditions. These five mechanisms make DHM a uniquely versatile nutraceutical active for products targeting alcohol support, liver health, anti-aging, metabolic wellness, and systemic inflammation.

Recommended DHM dosage: 300–600 mg for alcohol support — taken 30–60 minutes before or during alcohol consumption to enhance alcohol metabolism and reduce intoxication severity and hangover symptoms. For general health, antioxidant, and metabolic wellness applications: 100–300 mg daily. UPOR Biotech's DHM is extracted from Ampelopsis grossedentata (vine tea / 藤茶) leaves and standardized to ≥98% Dihydromyricetin by HPLC (Cosmetic/Nutraceutical Grade), with a ≥95% Standard Grade also available for cost-sensitive applications. Each batch is fully characterized by HPLC/UV with λmax at approximately 292 nm, confirming identity and purity against DHM reference standards. The extract is a pale yellow to off-white powder with a defined flavonoid profile dominated by DHM (≥98%), with minor accompanying Ampelopsis flavonoids including myricetin and dihydroquercetin (taxifolin). Full Certificate of Analysis (COA) with signed HPLC chromatogram is provided with every shipment. MOQ: 1 kg. Free sample available for qualified B2B buyers.

DHM, quercetin, resveratrol, and berberine target different and complementary therapeutic axes — they are not interchangeable. Quercetin is a broad-spectrum flavonoid antioxidant with strong radical scavenging (DPPH IC50 ~7 μg/mL) and anti-inflammatory activity via NF-κB inhibition, but lacks GABA-A receptor modulation entirely and has limited oral bioavailability without formulation enhancement — it cannot address alcohol-related applications. Resveratrol is a stilbenoid that activates SIRT1 and AMPK — the canonical longevity pathway — yet provides no alcohol interaction benefit and requires high oral doses (250–500 mg) for clinical effects due to rapid phase II glucuronidation and sulfation. Berberine is an isoquinoline alkaloid (not a flavonoid) with potent AMPK activation and mTOR inhibition for glucose and lipid regulation, but has very poor oral bioavailability (<5%) requiring specialized delivery systems. Dihydromyricetin (DHM) is uniquely positioned as the only flavonoid that combines GABA-A receptor positive allosteric modulation at the benzodiazepine site (directly reversing alcohol intoxication and hangover symptoms via α4β3δ subunit-preferring receptors), AMPK activation + mTOR inhibition (longevity and metabolic pathways via a distinct binding site), and potent antioxidant capacity from 8 phenolic -OH groups (DPPH IC50 ~6 μg/mL) — all in a single natural molecule from vine tea with centuries of safe traditional consumption history. DHM is not a replacement for quercetin, resveratrol, or berberine — it is a complementary multi-target flavonoid that addresses therapeutic gaps the others cannot fill, particularly alcohol-related, GABA-A-mediated, and hangover-reversal applications.

Every shipment of DHM includes comprehensive documentation: COA (HPLC purity ≥98.0%, full impurity profile, heavy metals ≤10 ppm with Pb ≤2 ppm / As ≤1 ppm / Hg ≤1 ppm / Cd ≤1 ppm, residual solvents per ICH Q3C, microbial panel — TAMC ≤1,000 CFU/g, TYMC ≤100 CFU/g, pathogens absent per USP standards), MSDS, HPLC Chromatogram (signed and dated with λmax ~292 nm confirmation), ISO 9001:2015 Certificate, ISO 22000 Certificate, HACCP Certificate, FDA Facility Registration, HALAL Certificate, KOSHER Certificate, Non-GMO Statement, Allergen Statement, BSE/TSE-Free Statement, Stability Data (25°C/60%RH real-time and 40°C/75%RH accelerated), and Complete Lot Traceability from Ampelopsis grossedentata raw leaf material to finished DHM powder. All documentation provided in English. Free sample available for qualified B2B buyers. MOQ: 1 kg. OEM and private label formulations available with flexible specifications.