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BiologicalX

Comparison

EGCG vs Ipamorelin

Side-by-side of EGCG and Ipamorelin. 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

Ipamorelin

  • Pentapeptide GHS-R1a agonist with the cleanest selectivity profile in the GHRP class
  • Minimal cortisol and prolactin elevation at standard doses (substantially less than GHRP-2 or hexarelin)
  • ~2 hour plasma half-life, longest of the synthetic GHRPs
  • Largest human safety database (~600 participants in Helsinn's postoperative ileus phase 2)
  • Standard pairing for CJC-1295 no-DAC at 200 to 300 mcg subcutaneously 2 to 3 times daily
  • Banned by WADA under S2; never reached registration despite phase 2b development

Side-by-side

Attribute EGCG Ipamorelin
Category natural peptide
Also known as epigallocatechin gallate, green tea extract NNC 26-0161, Aib-His-D-2-Nal-D-Phe-Lys-NH2
Half-life (hr) 3 2
Typical dose (mg) 400 0.2
Dosing frequency 1 to 2 times daily with food 2-3x daily
Routes oral subcutaneous, intravenous
Onset (hr) 1.5 0.25
Peak (hr) 2 1
Molecular weight 458.37 711.86
Molecular formula C22H18O11 C38H49N9O5
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. Selective GHS-R1a agonist that stimulates pulsatile GH release with minimal cortisol or prolactin co-activation. Suppresses hypothalamic somatostatin and stimulates pituitary somatotrophs.
Legal status Dietary supplement; warning labels required above 800 mg/day in some EU jurisdictions Not FDA approved; advanced through phase 2b in postoperative ileus before discontinuation; research-use-only grey market; banned by WADA
WADA status allowed banned
DEA / Rx Not scheduled Not scheduled (research chemical)
Pregnancy Avoid high-dose extracts; moderate green tea consumption appears acceptable Insufficient data; not recommended
CAS 989-51-5 170851-70-4
PubChem CID 65064 11338566
Wikidata Q307091 Q1666741

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)

Ipamorelin

Common side effects

  • injection-site irritation
  • vivid dreams
  • transient mild head pressure
  • occasional headache

Contraindications

  • pregnancy
  • active malignancy
  • history of pituitary tumor
  • uncontrolled diabetes

Interactions

  • CJC-1295: synergistic GH release via parallel GHRH and ghrelin pathways; standard pairing(minor)
  • sermorelin: additive GH release; functionally similar pairing to CJC-1295 with shorter GHRH half-life(minor)
  • insulin: sustained GH can blunt insulin sensitivity over weeks(moderate)
  • corticosteroids: blunt GH response; reduce expected efficacy(moderate)

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. Ipamorelin 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 growth-hormone axis, pick Ipamorelin.
  • If your priority is post-training recovery, pick Ipamorelin.

Edge case: If you want to avoid research-only / gray-market sourcing, EGCG is the more accessible choice.

Default choice: EGCG. Lower friction to source, and broader goal coverage. Reach for Ipamorelin 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 Ipamorelin?

EGCG and Ipamorelin differ in category (natural vs peptide), mechanism, and typical dosing. See the side-by-side table for full details.

Which has a longer half-life, EGCG or Ipamorelin?

EGCG half-life is 3 hours; Ipamorelin half-life is 2 hours.

Can you stack EGCG with Ipamorelin?

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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