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Tesamorelin 5MG

EGRIFTATH9507
A 44-amino acid GHRH analog that stimulates pituitary gh secretion, studied for visceral adipose tissue reduction in clinical research.

$50.00

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๐Ÿ”ฌ
50+
Published Studies
GHRH analog research papers
๐Ÿงฌ
44
Amino Acids
Full-length GHRH(1-44) analog
โš—๏ธ
2010
FDA Approval (Egrifta)
HIV-associated lipodystrophy
โœ…
99%+
Purity Verified
HPLC tested, COA included

How It Works

GHRH receptor signaling studied across metabolic, body composition, and cognitive research models

GHRH-R Agonism

Growth Hormone Secretagogue

Tesamorelin is a synthetic trans-3-hexenoic acid-modified analog of human GHRH(1-44). It binds and activates pituitary GHRH receptors, stimulating endogenous growth hormone (GH) secretion while preserving normal pulsatile GH release patterns โ€” unlike exogenous GH administration.

  • Selective GHRH receptor agonism
  • Preserves pulsatile GH secretion physiology
  • Stimulates downstream IGF-1 production
Lipolysis

Visceral Adipose Reduction

Clinical evidence demonstrates tesamorelin reduces visceral adipose tissue (VAT) through GH-mediated lipolytic pathways. GH activates hormone-sensitive lipase in adipocytes, promoting free fatty acid release from visceral fat depots. This mechanism underlies its FDA-approved indication for HIV-related lipodystrophy.

  • Stimulates GH-dependent hormone-sensitive lipase activity
  • Selectively targets visceral (not subcutaneous) fat
  • Preserves lean body mass in research models
Neuroprotection

Cognitive & Brain Research

Emerging research explores tesamorelin's effects on brain structure and function via IGF-1 signaling. Studies in older adults with mild cognitive impairment report changes in regional gray matter volume and functional connectivity. GH/IGF-1 axis modulation is hypothesized to support neuroplasticity mechanisms.

  • Increases circulating IGF-1, which crosses the blood-brain barrier
  • Associated with changes in cortical gray matter volume
  • Under investigation for cognitive aging research models
๐Ÿ“Š

What Research Has Shown

Key findings from Phase III trials and preclinical publications

Visceral Adipose Tissue Reduction (Phase III) ~15%
IGF-1 Level Increase ~100%
Trunk Fat Area Reduction ~18%
Lean Body Mass Preservation Maintained
๐ŸŽฏ

Research Applications

Primary areas of investigation

METABOLIC

Visceral Fat & Body Composition

Phase III trials confirmed significant reductions in visceral adipose tissue in HIV+ adults with abdominal fat accumulation. Mechanism involves GH-driven lipolysis in the visceral depots without disproportionate effects on subcutaneous fat.

Falutz et al. 2010 โ†—
COGNITIVE RESEARCH

Brain Structure & Function

Randomized controlled trials in older adults with mild cognitive impairment report tesamorelin's effects on regional brain volume and cognitive performance, mediated through elevated IGF-1 signaling.

Baker et al. 2019 โ†—
ENDOCRINOLOGY

GH/IGF-1 Axis

Research model for studying GHRH receptor pharmacology, GH secretagogue effects, and downstream IGF-1 modulation in the context of GH deficiency states and aging-related GH decline.

Stanley et al. 2011 โ†—
CARDIOMETABOLIC

Lipid & Cardiovascular Markers

Studies report tesamorelin's effects on triglycerides, non-HDL cholesterol, and carotid intima-media thickness in HIV-positive adults, supporting research into GH-axis modulation of cardiovascular risk markers.

Falutz et al. 2016 โ†—
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Compound Information

Technical specifications

Chemical Name Trans-3-hexenoic acidโ€“GRF(1-44)-amide
Sequence Modified GHRH(1-44) analog (44 amino acids)
Molecular Weight 5135.8 Da
Molecular Formula Cโ‚‚โ‚‚โ‚Hโ‚ƒโ‚†โ‚†Nโ‚‡โ‚‚Oโ‚†โ‚‡S

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