Handbook/Weight Loss & Metabolic/HGH Fragment 176-191

HGH Fragment 176-191

Also known as: Frag 176-191, AOD-9401, GH Fragment

The fat-burning fragment of human growth hormone without anabolic effects.

Overview

HGH Fragment 176-191 represents the tail portion of the HGH molecule responsible for its lipolytic effects. Unlike full HGH, this fragment does not compete for GH receptors or affect IGF-1 levels, providing targeted fat loss benefits.

Mechanism of Action

Mimics the lipolytic region of growth hormone, directly stimulating fat cell breakdown through beta-adrenergic mechanisms. Does not affect glucose metabolism or cellular proliferation.

Pharmacokinetics

Very short half-life (15-30 minutes) requiring multiple daily doses for optimal effect.

Dosing Protocols

Note: These are research protocols from literature. This is not medical advice.

1

Standard

Dose

250-500 mcg

Frequency

Twice daily

Duration

8-12 weeks

Morning and pre-exercise, fasted

Stacking Recommendations

Peptides that may be combined based on complementary mechanisms in research settings.

Rationale: Enhanced metabolic effect

Synergy: Full GH benefits plus targeted fat loss

Rationale: Body composition

Synergy: GH pulse plus fragment lipolysis

Research Areas

Fat LossBody CompositionMetabolic Research

Key Research Findings

  • 1Demonstrated lipolytic activity without hyperglycemia
  • 2No effect on longitudinal growth or IGF-1
  • 3Preferential reduction in abdominal fat in animal studies

Side Effects & Contraindications

Reported Side Effects

  • Injection site reactions
  • Hypoglycemia (rare)

Contraindications

  • Pregnancy
  • Active malignancy

Safety Considerations

Limited human data. Theoretically safer than full HGH due to lack of growth-promoting effects.

Storage Requirements

Store lyophilized at -20C. Reconstituted stable at 2-8C for 14 days.

Scientific References

Quick Reference

Sequence
Leu-Arg-Ile-Val-Gln-Cys-Arg-Ser-Val-Glu-Gly-Ser-Cys-Gly-Phe
Molecular Weight
1817.12 g/mol
Half-Life
15-30 minutes
Bioavailability
High (SC)
Research Stage
clinical phase 2
Administration
Subcutaneous injection