Fragment 176-191 + CJC-1295 + Ipamorelin
The Fragment 176-191 + CJC-1295 + Ipamorelin blend is a three-peptide research formulation that combines HGH Fragment 176-191, a 16-residue C-terminal piece of human growth hormone, with CJC-1295 without DAC, a GHRH analogue, and ipamorelin, a ghrelin receptor agonist. It is supplier-defined, not an approved or standardized product, and the combination has not been studied.
Last reviewed · Identity data matched to PubChem · 11 peer-reviewed sources
Key facts
- Components: HGH Fragment 176-191, CJC-1295 without DAC (Mod GRF 1-29) and ipamorelin
- Classes: hGH C-terminal fragment plus a GHRH analogue and a GHS-R1a agonist
- Commonly listed as a 12 mg vial by total content; split not standardized
- Molecular weights: fragment 1799.1; CJC-1295 no DAC 3367.9; ipamorelin 711.9 g/mol
- The fragment is studied for metabolic effects, not for stimulating GH release
- No published study of the three-peptide combination found in the PubMed records reviewed
- None of the three components is FDA approved
Chemical Identity
| Components | HGH Fragment 176-191 + CJC-1295 without DAC (Mod GRF 1-29) + Ipamorelin |
|---|---|
| Compound type | Blend |
What Is the Fragment 176-191 + CJC-1295 + Ipamorelin Blend?
The Fragment 176-191 + CJC-1295 + Ipamorelin blend is a supplier-defined, three-peptide formulation that combines a C-terminal fragment of human growth hormone with two growth hormone secretagogues: CJC-1295 without DAC (Mod GRF 1-29) and ipamorelin. It is commonly listed as a 12 mg vial by total content, and the listings tracked here do not state a standard split among the three peptides.
HGH Fragment 176-191 reproduces residues 176-191 of human growth hormone; synthetic C-terminal hGH peptides including this sequence were tested in rats as early as 1978[1]. CJC-1295 without DAC is a GHRH analogue, and ipamorelin is a pentapeptide described as the first selective growth hormone secretagogue[2].
The blend name says only “CJC-1295”. In this catalog it refers to the form without DAC; CJC-1295 with DAC is a distinct molecule carrying an albumin-binding lysine extension[3]. The combination is not an approved or standardized product.
Components at a Glance
Two components act on pituitary receptors that control growth hormone release; the third is a growth hormone fragment studied for metabolic effects rather than GH release.
| Component | Class | Primary target or mechanism studied | Molecular weight (g/mol) |
|---|---|---|---|
| HGH Fragment 176-191 | Synthetic C-terminal fragment of human GH (16 residues) | No receptor defined in the cited sources; studied for effects on glucose, insulin and fat metabolism in rodents[1][4] | 1799.1 |
| CJC-1295 without DAC (Mod GRF 1-29) | GHRH analogue (29 residues, four substitutions) | GRF (GHRH) receptor on the anterior pituitary, shown for hGRF(1-29) derivatives[3] | 3367.9 |
| Ipamorelin | Growth hormone secretagogue | Ghrelin receptor (GHS-R1a) agonist[5] | 711.9 |
Molecular weights are PubChem values (CIDs 16131230, 56841945 and 9831659).
Why These Compounds Are Studied Together
CJC-1295 and ipamorelin act on two different receptors in the growth hormone axis, while Fragment 176-191 is studied for a separate, metabolic line of research. No study of this three-peptide combination was found, and no cited source tests the fragment alongside either secretagogue.
The secretagogue pair
Ipamorelin releases GH through a GHRP-like receptor rather than the GHRH receptor, as shown by profiling with GHRP and GHRH antagonists[2]. In rats treated with ipamorelin for 15 days, the pituitary GH response to GHRH was unchanged[6]. A 2026 review reported that CJC-1295 combined with ipamorelin improved maximum tetanic tension in a mouse model of glucocorticoid-induced muscle loss, limited to animal work; the abstract does not state which CJC-1295 form was used[7].
The fragment
The C-terminal hGH domain has been studied for direct effects on fat tissue. The closely related 177-191 analog AOD-9401 stimulated hormone-sensitive lipase and inhibited acetyl-CoA carboxylase in isolated rat adipose tissue, and reduced body weight gain in obese Zucker rats without inducing insulin resistance[4]. In normal rats, however, the 176-191 sequence itself produced a short-lived rise in blood glucose and a more sustained rise in plasma insulin[1]. These data come from rodents and concern the fragment alone.
Why they appear together
The grouping reflects how these peptides are marketed more than any tested rationale. A 2026 review lists Frag 176-191, ipamorelin and CJC-1295 among peptides promoted for muscle growth and fat metabolism, and notes that most published studies do not examine the combined protocols common in bodybuilding[8].
With three peptides and easily confused fragment names, researchers typically check HPLC and mass spectrometry certificates of analysis that confirm each sequence.
Research Status
The Fragment 176-191 + CJC-1295 + Ipamorelin blend has no regulatory approval and is supplied for laboratory research use only. None of its three components is FDA approved, and a 2026 review notes the absence of regulatory approval for physique- or performance-related uses of GH-axis peptides[9].
hGH 176-191 is among the prohibited peptides targeted by a 2026 doping-control detection workflow[10]. Forensic analyses of seized material have identified glycine-modified analogues of ipamorelin and modified GRF 1-29[11], and unregulated peptide products are often mislabeled or contaminated[8]. Naming adds confusion: the review cited above refers to the GH fragment as “AOD9604 (hGH 176-191)”, although AOD-9604 is a modified 177-191 sequence[9].
Evidence quality is low: rodent and in vitro data for the fragment, mainly animal data for ipamorelin, limited peer-reviewed data for CJC-1295 without DAC, and no published data on the combination.
Commonly Supplied Research Formats
Fragment 176-191 + CJC-1295 + Ipamorelin is listed by 2 of the 11 major U.S. research-peptide suppliers we track. The most commonly listed formats are:
- 12mg
Supplier catalog survey, October 2026. Quantities refer to net peptide per vial as labeled.
Frequently Asked Questions
What is in the Fragment 176-191 + CJC-1295 + Ipamorelin blend?
The blend contains three peptides: HGH Fragment 176-191, a 16-residue sequence from the C-terminus of human growth hormone; CJC-1295 without DAC, a substituted 29-residue GHRH analogue; and ipamorelin, a five-residue ghrelin receptor agonist. It is commonly listed as a 12 mg vial by total content, with no standardized ratio among the components.
Is Fragment 176-191 a growth hormone secretagogue?
No. Unlike CJC-1295 and ipamorelin, Fragment 176-191 is not studied as a stimulator of GH release. It is a piece of the growth hormone molecule itself, researched in rodents for effects on glucose, insulin and fat metabolism. Most lipolysis data come from the related 177-191 analog AOD-9401 rather than the 176-191 sequence.
Is Fragment 176-191 the same as AOD-9604?
No, though the names are often mixed up. Fragment 176-191 is hGH residues 176-191. AOD-9401 is the shorter 177-191 sequence, and AOD-9604 adds a tyrosine to that 177-191 sequence. Some reviews still label the GH fragment as "AOD9604 (hGH 176-191)", so the exact sequence should be checked in any source or product document.
Has the Fragment 176-191 + CJC-1295 + Ipamorelin combination been studied?
No study of this three-peptide combination was found in the PubMed records reviewed. A review reports one mouse study of CJC-1295 with ipamorelin, and separate rodent studies cover the hGH C-terminal fragment. No cited study gives the fragment together with either secretagogue, so effects of the combined formulation are unknown.
References
- Ng FM, Bornstein J. Hyperglycemic action of synthetic C-terminal fragments of human growth hormone. The American journal of physiology 1978. PMID 645904 · DOI
- Raun K, Hansen BS, Johansen NL, et al. Ipamorelin, the first selective growth hormone secretagogue. European journal of endocrinology 1998. PMID 9849822 · DOI
- Jetté L, Léger R, Thibaudeau K, et al. Human growth hormone-releasing factor (hGRF)1-29-albumin bioconjugates activate the GRF receptor on the anterior pituitary in rats: identification of CJC-1295 as a long-lasting GRF analog. Endocrinology 2005. PMID 15817669 · DOI
- Ng FM, Jiang WJ, Gianello R, et al. Molecular and cellular actions of a structural domain of human growth hormone (AOD9401) on lipid metabolism in Zucker fatty rats. Journal of molecular endocrinology 2000. PMID 11116208 · DOI
- Lu Z, Ngan MP, Liu JYH, et al. The growth hormone secretagogue receptor 1a agonists, anamorelin and ipamorelin, inhibit cisplatin-induced weight loss in ferrets: Anamorelin also exhibits anti-emetic effects via a central mechanism. Physiology & behavior 2024. PMID 39043357 · DOI
- Johansen PB, Nowak J, Skjaerbaek C, et al. Ipamorelin, a new growth-hormone-releasing peptide, induces longitudinal bone growth in rats. Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society 1999. PMID 10373343 · DOI
- Mayfield CK, Bolia IK, Feingold CL, et al. Injectable Peptide Therapy: A Primer for Orthopaedic and Sports Medicine Physicians. The American journal of sports medicine 2026. PMID 41476424 · DOI
- Coutinho LFD, DE Oliveira Neves LF, Camilo RP. A new era of doping? Use of peptide and peptide-analog drugs in recreational and professional sport and bodybuilding: a critical review. The Journal of sports medicine and physical fitness 2026. PMID 41880199 · DOI
- Dominikowski A, Rękoś Z, Olejarz M, et al. The emerging landscape of performance-enhancing peptides modulating GH-IGF1 axis: bridging the gap between clinical evidence and patient self-administration. Frontiers in endocrinology 2026. PMID 42395176 · DOI
- Mazzarino M, Colpaert T, Deventer K, et al. Rapid and harmonized analytical workflow for the determination of peptidic and non-peptidic doping agents in dried and liquid blood matrices. The Analyst 2026. PMID 42328738 · DOI
- Gajda PM, Holm NB, Hoej LJ, et al. Glycine-modified growth hormone secretagogues identified in seized doping material. Drug testing and analysis 2019. PMID 30136411 · DOI
Related Compounds
This profile summarizes chemical data and peer-reviewed literature for educational and laboratory-research reference. It is not medical advice, and nothing here describes or recommends use in humans or animals. How we source and verify data.