Home/Growth Hormone/CJC-1295 with DAC vs Tesamorelin

CJC-1295 with DAC vs Tesamorelin

GHRH analog · Drug Affinity Complex against stabilised GHRH(1-44) analog. Every row below is read from the two product records and the papers verified for each; nothing here is an opinion about which is better.

At a glance

CJC-1295 with DACTesamorelin
What it isGHRH analog · Drug Affinity ComplexStabilised GHRH(1-44) analog
GroupGrowth HormoneGrowth Hormone
Molecular formulaC165H269N47O46C221H366N72O67S
Molecular weight3647.15 g/mol5135.86 g/mol
CAS863288-34-0218949-48-5
Cited literature2 human studies cited3 human studies cited
Studies cited2 human · 0 animal · 0 cell · 0 review3 human · 0 animal · 0 cell · 0 review
CertificateThird-party report for lot CS-cwd5-0327, 98.882% purity, verification key MDNS5VV6SH3WThird-party report for lot CS-te10-0408, 99.676% purity, verification key MPW66QXY18MA
Sizes and price10mg $10010mg $80 · 20mg $100 (out of stock)
AvailabilityIn stockIn stock
StorageLyophilised, −20°C, darkLyophilised, −20°C, dark

CJC-1295 with DAC

A tetrasubstituted GHRH(1-29) analog bearing a Drug Affinity Complex, which binds serum albumin and dramatically extends circulating half-life versus the no-DAC form.

CJC-1295 with DAC is a synthetic peptide with the molecular formula C165H269N47O46 and a molecular weight of 3647.15 g/mol, CAS registry number 863288-34-0. The vial is sealed and lot-numbered, holds lyophilised powder, and is kept at −20°C protected from light until it ships.

CJC-1295 is an analog of the first 29 residues of growth-hormone-releasing hormone. DAC stands for Drug Affinity Complex, a chemical modification that lets the molecule bind serum albumin and circulate far longer than the unmodified peptide. The DAC and non-DAC forms are distinct compounds.

The 2 papers cited below are 2 studies in humans.

Cited on the CJC-1295 with DAC page

  1. Teichman SL et al. (2006). Prolonged stimulation of growth hormone (GH) and insulin-like growth factor I secretion by CJC-1295, a long-acting analog of GH-releasing hormone, in healthy adults. J Clin Endocrinol Metab. PubMed 16352683 · SummaryHealthy adults: a single dose raised growth hormone for at least six days and IGF-1 for nine to eleven days; estimated half-life 5.8–8.1 days.
  2. Ionescu M & Frohman LA (2006). Pulsatile secretion of growth hormone (GH) persists during continuous stimulation by CJC-1295, a long-acting GH-releasing hormone analog. J Clin Endocrinol Metab. PubMed 17018654 · SummaryGrowth hormone remained pulsatile under CJC-1295: trough and mean levels rose while pulse frequency was unchanged.

Tesamorelin

A 44-amino-acid GHRH analog stabilised against enzymatic degradation. The most clinically characterised growth hormone releasing hormone in research use.

Tesamorelin is a synthetic peptide with the molecular formula C221H366N72O67S and a molecular weight of 5135.86 g/mol, CAS registry number 218949-48-5. The vial is sealed and lot-numbered, holds lyophilised powder, and is kept at −20°C protected from light until it ships.

Tesamorelin is a growth-hormone-releasing-hormone analog. A pharmaceutical form is FDA-approved under the name Egrifta for one specific indication. The research vial sold here is not that product and is not manufactured to its standard.

The 3 papers cited below are 3 studies in humans.

Cited on the Tesamorelin page

  1. Falutz J et al. (2007). Metabolic effects of a growth hormone-releasing factor in patients with HIV. N Engl J Med. PubMed 18057338 · SummaryHIV patients with abdominal fat accumulation, 26 weeks: visceral adipose tissue fell about 15% against a rise on placebo.
  2. Falutz J et al. (2010). Effects of tesamorelin (TH9507), a growth hormone-releasing factor analog, in human immunodeficiency virus-infected patients with excess abdominal fat: a pooled analysis of two multicenter, double-blind placebo-controlled phase 3 trials with safety extension data. J Clin Endocrinol Metab. PubMed 20554713 · SummaryPooled analysis of two phase 3 trials: the visceral fat reduction held through 52 weeks of continued treatment and reversed on withdrawal.
  3. Stanley TL et al. (2019). Effects of tesamorelin on non-alcoholic fatty liver disease in HIV: a randomised, double-blind, multicentre trial. Lancet HIV. PubMed 31611038 · SummaryTwelve-month trial in HIV-associated liver fat: hepatic fat fraction fell and fewer participants progressed in fibrosis.

Handling the two side by side

CJC-1295 with DAC

  • Lyophilised powder is stable for years at −20°C in the dark and tolerates days at ambient temperature in transit.

Tesamorelin

  • Lyophilised powder is stable for years at −20°C in the dark and tolerates days at ambient temperature in transit.

Where to go next

Research use only This page compares two laboratory materials by their published record and their chemistry. It is not a recommendation of either, nothing here is dosing guidance, and nothing sold by Zyrna Research is for human or veterinary use.