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Comparison

EGCG vs Low-Dose Naltrexone

Side-by-side of EGCG and Low-Dose Naltrexone. Every row below is pulled from the compound schema and will update as our data grows. For deeper reads, follow through to each compound page.

Effects at a glance

EGCG

  • Modest fat loss (~1.3 kg over 12 weeks) when combined with caffeine and caloric deficit
  • Small reductions in LDL cholesterol (3-6 mg/dL) and systolic blood pressure (2-3 mmHg)
  • EFSA flags hepatotoxicity risk above 800 mg/day, particularly when taken fasted
  • Bioavailability is 0.1-1.0%; gut microbiome variation drives population-variable response
  • Green tea extract typically combines EGCG with caffeine and L-theanine for additive effects
  • Reduces non-heme iron absorption when co-administered with meals

Low-Dose Naltrexone

  • Off-label use at 1.5 to 4.5 mg, roughly one-tenth the FDA-approved 50 mg addiction-treatment dose
  • Proposed mechanisms include brief opioid receptor blockade triggering rebound endogenous opioid release, plus TLR4 antagonism
  • Compounded prescription only; insurance rarely covers; cash prices 20 to 80 USD per month
  • Younger 2013 reported ~30% pain reduction in fibromyalgia at 4.5 mg in a small crossover trial
  • Smith 2011 reported endoscopic improvement in active Crohn's disease (n=40 placebo-controlled)
  • Vivid dreams affect 20 to 40% in first 2 weeks; manageable by switching to morning dosing

Side-by-side

Attribute EGCG Low-Dose Naltrexone
Category natural pharmaceutical
Also known as epigallocatechin gallate, green tea extract LDN, naltrexone (low dose)
Half-life (hr) 3 4
Typical dose (mg) 400 4.5
Dosing frequency 1 to 2 times daily with food once daily, typically at bedtime
Routes oral oral
Onset (hr) 1.5 1
Peak (hr) 2 1.5
Molecular weight 458.37 341.4
Molecular formula C22H18O11 C20H23NO4
Mechanism Inhibits catechol-O-methyltransferase (COMT) to prolong norepinephrine signaling; activates AMPK; scavenges reactive oxygen species via gallate ester; modulates gut microbiome and pancreatic lipase activity. Brief mu-opioid receptor antagonism proposed to trigger compensatory upregulation of endogenous opioids; secondary TLR4 antagonism on microglia and immune cells contributes to anti-inflammatory effect.
Legal status Dietary supplement; warning labels required above 800 mg/day in some EU jurisdictions Off-label compounded prescription (naltrexone is FDA approved for opioid and alcohol use disorder at 50 mg)
WADA status allowed allowed
DEA / Rx Not scheduled Rx only (not a controlled substance)
Pregnancy Avoid high-dose extracts; moderate green tea consumption appears acceptable Insufficient data; not routinely recommended
CAS 989-51-5 16590-41-3
PubChem CID 65064 5360515
Wikidata Q307091 Q426444

Safety profile

EGCG

Common side effects

  • nausea
  • abdominal discomfort
  • diarrhea
  • jitteriness (with caffeine)
  • sleep disruption (with caffeine)

Contraindications

  • pregnancy at high-dose extracts
  • active liver disease
  • iron deficiency anemia (separate dosing)

Interactions

  • iron supplements: reduces non-heme iron absorption; separate by 2 to 3 hours(moderate)
  • anticoagulants: additive effects at high catechin doses(minor)
  • beta-blockers (nadolol): reduced absorption when taken simultaneously(moderate)
  • hepatotoxic supplements (high-dose niacin, kava): theoretical additive hepatotoxicity at high EGCG doses(moderate)
  • stimulants and caffeine: additive thermogenic and cardiovascular effects(minor)

Low-Dose Naltrexone

Common side effects

  • vivid dreams
  • sleep disruption
  • headache
  • mild GI upset
  • fatigue (early)

Contraindications

  • concurrent opioid use
  • acute hepatitis or liver failure
  • opioid dependence
  • pregnancy (insufficient data)

Interactions

  • opioid analgesics (oxycodone, morphine, codeine): blocks analgesic effect; precipitates withdrawal in dependent users(major)
  • tramadol: blocks opioid component of analgesia(major)
  • thyroid hormone replacement: may alter dose requirements after immune modulation; monitor TSH(minor)

Which Should You Take?

EGCG comes out ahead for most readers on the criteria we weight: 3 catalogued goals, OTC dietary supplement, oral dosing, with a Tier-B outcome catalogued. Low-Dose Naltrexone is the right call when one of the conditionals below applies.

  • If your priority is metabolic health and glucose control, pick EGCG.
  • If your priority is healthspan extension, pick EGCG.
  • If your priority is immune support, pick Low-Dose Naltrexone.
  • If your priority is pain modulation, pick Low-Dose Naltrexone.

Edge case: If you want to avoid prescription-only, EGCG is the more accessible choice.

Default choice: EGCG. Lower friction to source, and broader goal coverage. Reach for Low-Dose Naltrexone only if your priority sits squarely in the goals it owns above.

This verdict is generated from each compound's schema (goals, legal status, evidence outcomes, dosing route). It updates automatically as our compound data evolves; the deeper read sits on each individual compound page.

Common questions

What is the difference between EGCG and Low-Dose Naltrexone?

EGCG and Low-Dose Naltrexone differ in category (natural vs pharmaceutical), mechanism, and typical dosing. See the side-by-side table for full details.

Which has a longer half-life, EGCG or Low-Dose Naltrexone?

EGCG half-life is 3 hours; Low-Dose Naltrexone half-life is 4 hours.

Can you stack EGCG with Low-Dose Naltrexone?

Stack compatibility depends on mechanism overlap, legal status, and individual response. Check each compound page for specific interactions and contraindications before combining.

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