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| Attribute | ||
|---|---|---|
Research Summary | Tesamorelin is the only growth hormone booster specifically proven to target and melt away hard, stubborn belly fat (visceral fat). It was literally FDA-approved just for this purpose. | This is literally just the fat-burning piece of human growth hormone cut off from the rest. Because it is only the fat-burning piece, it burns fat rapidly without causing muscles to grow or affecting your blood sugar. |
Studied For | HIV-associated lipodystrophy (FDA approved)Hepatic fat / NAFLD researchCognition research in aging/HIVGH deficiencyBody composition improvementVisceral adipose reductionLiver fat reductionGH axis stimulationIGF-1 elevationCardiovascular lipid profile improvementCognitive decline in aging HIV+ populationAnti-aging via GH axisNon-alcoholic fatty liver diseaseLean mass supportvisceral fat reductionbelly fatHIV lipodystrophymuscle growthbody compositionlipid profile improvementcognitive function | Lipolysis / fat lossAdipose reductionVisceral fat reductionBody composition improvementSubcutaneous fat burningFat oxidationAnti-obesity researchWeight managementMetabolic rate enhancementFat-loss peptide researchAbdominal fat researchBeta-3 adrenergic lipolysisLean mass preservation during fat lossGH-fragment weight research |
Research Areas | Performance & MuscleMetabolicWeight Management & Fat LossJoint & Bone SupportCognitive | MetabolicWeight Management & Fat Loss |
Best Stacked With | ipamorelincjc-1295-no-dacl-carnitinebac-water | aod9604l-carnitinelipo-cbac-water |
Overview | ||
Category | Muscle Growth & Performance | Muscle Growth & Performance |
Compound Class | Synthetic GHRH analog with trans-3-hexenoic acid modification at N-terminus; FDA-approved for HIV lipodystrophy | Synthetic fragment of HGH C-terminus (residues 176-191) |
Molecular Target | GHRH receptor (GHRHR) on pituitary somatotrophs; GH/IGF-1 axis stimulation; preferential visceral fat metabolism | Beta-3 adrenergic receptors; stimulates lipolysis without GH receptor binding; no IGF-1 elevation |
Aliases / AKA | EgriftaEgrifta SVTH9507Tesamorelin acetateTrans-3-hexenoic acid GHRHModified GHRH analog Egrifta | HGH FragAOD FragmentFrag 176-191HGH FragmentFragment 176-191HGH 176-191 |
Parent Compound | Growth hormone releasing hormone | Human growth hormone |
Molecular Weight | 5135.9 Da | 1817.1 Da |
Amino Acid Sequence | hGHRH(1-44) with trans-3-hexenoyl | 16-aa C-terminal lipolytic fragment of human growth hormone (residues 176-191) |
CAS Number | 218949-48-5 | 66004-57-7 |
Year Discovered | Not Listed | Not Listed |
Pro-Angiogenic | No | No |
GLP-1 Class | No | No |
Purity | Not Listed | Not Listed |
Identity | ||
Evidence Tier | ||
Risk Level | ||
PubMed Citations | 125 Moderate | 23 Sparse |
Clinical Trials | 1010 Active | Not Listed |
Regulatory Status | FDA-approved (Egrifta) for HIV lipodystrophy; WADA S2. | Not FDA-approved; research chemical; WADA-banned. |
Evidence & Regulatory | ||
Half-Life | ~26-38 minutes | ~3 minutes |
Typical Frequency | Not Listed | Not Listed |
Administration Route | Injection Only | Injection Only |
Mechanism / PK | Not Listed | Not Listed |
Reported Findings | Strong human randomized trials show roughly 15 to 18 percent visceral-fat reduction over 26 weeks with reduced triglycerides and reduced liver fat. It is FDA-approved for HIV-associated lipodystrophy. | Obese-mouse studies show reduced weight and increased fat oxidation. Human evidence for the fragment is minimal; most human data come from the related AOD9604, which was ultimately not significant. |
Side Effects Noted | Joint pain, injection-site reactions, peripheral edema, paresthesia, reduced glucose tolerance and elevated IGF-1. | Limited formal human safety data; mainly injection-site reactions in unregulated use; long-term safety uncharacterized. |
Warnings | Contraindicated in active malignancy, pituitary disorders, and pregnancy; monitor IGF-1 and glucose. Benefit reverses on discontinuation. WADA-prohibited (needs a therapeutic-use exemption). | Not approved; human efficacy unproven; grey-market identity and purity are a major limitation. WADA-banned. Research use only. |
Pharmacology | ||
Form | lyophilized | lyophilized |
Diluent | sterile water | bacteriostatic water; slow, no foaming |
Storage Temp | per formulation (room temp or refrigerated); follow label | -20C, dark |
Light Sensitive | Yes | Yes |
Freeze / Thaw | avoid | avoid |
Handling Notes | Daily subcutaneous; improper reconstitution causes aggregation. | Disulfide loop is oxidation-sensitive. |
Reconstituted Shelf Life | 1 Days Refrigerated | 28 Days Refrigerated |
Handling & Storage | ||
Pep Nation Lab's comparison tool puts research-grade peptides and compounds head to head - mechanism of action, molecular target, evidence tier, molecular weight, sequence, half-life, and documented research focus - so qualified researchers can evaluate the differences that matter. Every data point is drawn from a referenced monograph. For in vitro laboratory research use only.
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Browse the full research catalog or the A To Z index to compare any compound.
Any research-grade compound in the library can be placed side by side - up to four at a time. The tool compares mechanism of action, molecular target, evidence tier, molecular weight, amino acid sequence, reported half-life, and what each compound has been studied for, all drawn from referenced monographs.
The evidence tier reflects how extensively a compound has been studied in the referenced literature, from early preclinical signals through to compounds with human clinical data. It is a research-quality signal only, never a safety or efficacy endorsement.
Each comparison page is generated from the same referenced compound database - a genuine side-by-side of mechanism, identity, pharmacokinetics, and evidence, plus data-derived key differences. They are curated, not auto-generated thin pages.
No. Every comparison is for in vitro laboratory research use only. Nothing here is medical advice, a treatment recommendation, or dosing guidance, and no product is for human or animal consumption.