GHRP-2 + LUV TES + MGF + Ipamorelin
A four-component research blend of three short synthetic peptides and a 24-residue E-peptide fragment corresponding to a splice variant of the IGF-1 gene, characterized by sequence, molecular formula, and structural class.
Molecular Profile
- Type
- Peptide blend
Components
GHRP-2
- Molecular formula
- C45H55N9O6
- Molecular weight
- 817.97 g/mol
- CAS number
- 158861-67-7
- Sequence
- D-Ala-D-2-Nal-Ala-Trp-D-Phe-Lys-NH2
LUV TES
- Molecular formula
- C221H366N72O67S
- Molecular weight
- 5135.89 g/mol
- CAS number
- 218949-48-5
MGF
- Molecular formula
- C121H200N42O39
- Molecular weight
- 2888.16 g/mol
- Sequence
- YQPPSTNKNTKSQRRKGSTFEEHK
Ipamorelin
- Molecular formula
- C38H49N9O5
- Molecular weight
- 711.87 g/mol
- CAS number
- 170851-70-4
- Sequence
- Aib-His-D-2-Nal-D-Phe-Lys-NH2
Mechanism & Target Class
GHRP-2 and Ipamorelin are short synthetic peptides built largely from non-standard and D-configured residues. GHRP-2 is a hexapeptide (D-Ala-D-2-Nal-Ala-Trp-D-Phe-Lys-NH2) and Ipamorelin is a C-terminally amidated pentapeptide (Aib-His-D-2-Nal-D-Phe-Lys-NH2); both carry a class of small peptides that engage a G-protein-coupled receptor, and their D-amino-acid content and C-terminal amidation confer protease resistance. LUV TES is a large synthetic peptide whose sequence is based on a 44-residue hypothalamic peptide; a hexenoyl modification at the N-terminus distinguishes it structurally from the native sequence and stabilizes the molecule. MGF is a 24-residue C-terminal E-peptide fragment whose sequence (YQPPSTNKNTKSQRRKGSTFEEHK) corresponds to a mechanical-stress-induced splice variant of the IGF-1 gene (IGF-1Ec); its primary structure is distinct from that of full-length IGF-1.
Storage & Handling
- Lyophilized
- GHRP-2, MGF, Ipamorelin: -20°C to -80°C. LUV TES: 2–8°C.
- Handling
- Avoid repeated freeze-thaw cycles for GHRP-2, MGF, and Ipamorelin. Protect LUV TES from light.
References (18)
Reviews
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Primary research
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- 10
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Zhang B, Liu Z, Li X, et al. (2023). International Journal of Molecular Medicine
- 12
Venkova K, Mann W, Nelson R, et al. (2009). Journal of Pharmacology and Experimental Therapeutics
- 13
Dluzniewska J, Sarnowska A, Lee J, et al. (2005). FASEB Journal
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Laferrère B, Bressler P, David D, et al. (2002). Journal of Clinical Endocrinology & Metabolism
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Stanley TL, Fourman LT, Feldpausch MN, et al. (2019). Lancet HIV
DOI: 10.1016/S2352-3018(19)30338-8PubMed 31611038NCT02196831
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