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Peptide

Reference library

Educational peptide reference — research use only.

Research & educational use only

For laboratory and educational research only. Not for human or veterinary consumption. This is not medical advice. Always follow applicable laws and consult qualified professionals.

The calculator performs unit math for research reference. It must not be used to plan or guide dosing in humans or animals. Verify all figures independently in your lab protocol.

Tesamorelin

A GHRH analog studied in lipodystrophy and GH-axis research.

Half-life (approx.)
~26 min (approx., IV); subQ longer
Diluent
Bacteriostatic water (0.9% benzyl alcohol)
Common vials
2 mg

Half-life figures are literature approximations for educational reference — not pharmacokinetic advice.

Overview

Tesamorelin (TH9507) is an FDA-approved GHRH analog studied for HIV-associated lipodystrophy and visceral-fat reduction. It stimulates pulsatile GH release with a well-characterized pharmacokinetic profile in clinical literature. FDA-approved stabilized GHRH for HIV-associated visceral lipodystrophy research context.

Structure & identity

Stabilized GHRH analog — trans-3-hexenoic acid modified

Chemical name
(3E)-hex-3-enoylsomatoliberin
Sequence / structure
44-amino-acid synthetic GHRH analogue with N-terminal trans-3-hexenoic acid modification
Formula
C221H366N72O67S
Molecular weight
5136 g/mol
CAS
218949-48-5

Status: FDA-approved (Egrifta).

Mechanism

Tesamorelin binds GHRH receptors on anterior pituitary somatotrophs, activating G-protein-coupled signaling that increases endogenous growth hormone synthesis and pulsatile release. Downstream GH stimulates hepatic IGF-1 and IGFBP-3 production. Lipolytic GH effects preferentially reduce visceral adipose in lipodystrophy models while generally sparing subcutaneous fat.

Stabilized GHRH analog stimulates pulsatile GH to reduce visceral adipose in lipodystrophy research. Trans-3-hexenoic acid modification improves GHRH stability versus native fragment.

Studies & clinical programs

  • HIV-associated lipodystrophy Phase 3(Phase 3)

    HIV-infected adults on antiretroviral therapy with excess visceral adipose tissue

    • Significant reduction in visceral adipose tissue on MRI versus placebo over treatment periods.
    • Average ~15% reduction in excess visceral fat reported in pivotal analyses.
    • Improved triglyceride and metabolic parameters in extension studies.

    Source: Egrifta (tesamorelin) development program

  • Hepatic fat and body-composition substudies

    HIV-positive cohorts with metabolic comorbidity

    • Decreased liver fat fraction on imaging in 12-month substudies.
    • CT-based muscle density and area changes documented in paraspinal and psoas muscle groups.

    Source: Published lipodystrophy extension literature

Research models in literature

  • HIV lipodystrophy trials
  • Visceral adipose MRI endpoints

Literature highlights

  • Stabilized GHRH analog reduces visceral adipose in HIV lipodystrophy trials (Egrifta).
  • MRI visceral-fat and IGF-1 endpoints characterize metabolic effects.
  • FDA-approved GHRH — compared with CJC and sermorelin in GH-axis research.

Combination research notes

GH-axis blends combine tesamorelin with ipamorelin (Tesa+IPA mix in this library).

Key targets & pathways

GHRH receptorVisceral adipose tissueLipodystrophy MRI endpoints

Research areas

GHRH analogLipodystrophyVisceral fatGH pulsatility

Routes in research literature

Subcutaneous

Also known as

EgriftaTH9507

Stability & storage phases

PhaseConditionGuidance
LyophilizedSealed vial, refrigerated (2–8 °C)Intact lyophilized cake or powder is typically stable for months to years per published stability data; protect from moisture, light, and repeated freeze-thaw of the dry vial.
ReconstitutedBacteriostatic water (0.9% benzyl alcohol), refrigeratedMost aqueous peptide solutions remain usable for approximately 2–4 weeks refrigerated; verify published stability data and label with reconstitution date.
Working aliquotsPre-drawn syringes or microtubes, frozen (−20 °C)Aliquot promptly after mixing to limit freeze-thaw cycles on the main vial; thaw once and use to reduce protease-mediated degradation.

Stability windows are formulation-dependent — verify published data and your lab SOP.

Reconstitution reference table

Vial (mg)Diluent (mL)mcg/mLUnits @ 100 mcgUnits @ 250 mcgUnits @ 500 mcg
221000.0102550

U-100 insulin syringe scale (100 units = 1 mL). Illustrative only — not dosing guidance.

Reconstitution steps

  1. Allow vial to reach room temperature (15–30 min)
  2. Swab rubber stopper with alcohol prep pad
  3. Draw calculated bacteriostatic water into syringe
  4. Inject diluent slowly down vial wall — do not spray directly onto cake
  5. Gently swirl until fully dissolved — do not shake vigorously
  6. Label with date, concentration, and diluent volume
  7. Refrigerate and use within your lab stability window

Typically reconstituted with 1–2 mL bacteriostatic water.

Laboratory record checklist

  • Compound identity recorded in lab notebook (name, lot, preparation date)
  • Analytical identity cross-checked against published sequence or structure
  • Potency or concentration documented from analytical certificate when available
  • Purity or HPLC data filed when provided with research material
  • Appearance noted: intact lyophilized cake or uniform powder
  • Sterility / endotoxin report archived when available
  • Storage temperature applied immediately per published stability guidance