
4x Blend GHRP-2 (5mg) / Tesamorelin (5mg) / MGF (.5mg) / Ipamorelin (2.5mg)
$171.35
4x Blend GHRP-2 (5mg) / Tesamorelin (5mg) / MGF (.5mg) / Ipamorelin (2.5mg)
Islip
Pickup available, usually ready in 24 hours
3 Grant Ave.
Ste. B
Islip NY 11751
United States
+16316770030
Overview
Four-Time Blend is a proprietary research peptide formulation combining four synergistic compounds—GHRP-2 (Growth Hormone Releasing Peptide-2), Tesamorelin, MGF (Mechano Growth Factor), and Ipamorelin—intended exclusively for in vitro and preclinical research applications. This blend targets the growth hormone (GH) axis to investigate enhanced GH secretion, muscle repair, and metabolic modulation. It works by stimulating pituitary GH release through multiple pathways (GHSR agonism and GHRH mimicry), amplifying downstream IGF-1 signaling for tissue regeneration and lipolysis, without direct hormonal replacement.
Applications
Research Applications
• Investigating GH-mediated muscle hypertrophy and satellite cell activation in tissue engineering models.
• Exploring fat metabolism and lipodystrophy reversal in metabolic disorder cell cultures.
• Studying post-exercise recovery and anti-catabolic effects in myoblast proliferation assays.
• Evaluating anti-aging mechanisms, including collagen synthesis and sleep regulation in neuronal models.
• Probing synergistic GH secretagogue effects on appetite, energy homeostasis, and bone density in endocrine research.
Mechanism of Action
Mechanisms of Action
• GHRP-2: Acts as a ghrelin mimetic, binding to the growth hormone secretagogue receptor (GHSR) on pituitary somatotrophs to trigger pulsatile GH release via intracellular calcium mobilization and phospholipase C activation.
• Tesamorelin: A synthetic analog of growth hormone-releasing hormone (GHRH), it binds GHRH receptors (GHRHR) on the anterior pituitary, increasing cAMP levels to promote GH gene transcription and sustained release.
• MGF: As an alternative splice variant of IGF-1 (IGF-1Eb), it activates PI3K/Akt and MAPK pathways in muscle satellite cells, driving proliferation and migration for localized tissue repair without systemic GH elevation.
• Ipamorelin: A selective GHSR agonist, it induces GH secretion through Gq-protein-coupled receptor signaling, emphasizing pituitary-specific effects with minimal impact on cortisol or prolactin.
Key Research Studies
Tesamorelin
Tesamorelin is a growth hormone-releasing factor analog primarily studied for reducing visceral adipose tissue in HIV patients with lipodystrophy. Here are key research studies:
• 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 (2010): This pooled analysis of two phase-3 trials demonstrated significant reductions in visceral adipose tissue and improvements in lipid profiles. Link
• Effect of tesamorelin on visceral fat and liver fat in HIV-infected patients with abdominal fat accumulation: a randomized clinical trial (2014): A randomized trial showing tesamorelin reduced visceral and liver fat by 15-18% over 6 months, with benefits for metabolic health. Link
• The Growth Hormone Releasing Hormone Analogue, Tesamorelin, Decreases Muscle Fat and Increases Muscle Area in Adults with HIV (2019): This study found tesamorelin improved body composition by reducing muscle fat infiltration and increasing muscle cross-sectional area. Link
• Effects of Tesamorelin on Nonalcoholic Fatty Liver Disease in HIV (2020): Demonstrated a 40% relative reduction in hepatic fat, highlighting potential for treating NAFLD in HIV populations. Link
• Growth hormone and tesamorelin in the management of HIV-associated lipodystrophy (2011): Review of randomized trials confirming safety and efficacy in reducing central fat accumulation. Link
MGF (Mechano Growth Factor)
MGF, a splice variant of IGF-1, is researched for its roles in muscle repair, proliferation, and tissue regeneration post-injury. Key studies include:
• Mechano-Growth Factor: an important cog or a loose screw in the repair machinery? (2012): Comprehensive review on MGF’s specific actions in muscle development, growth, repair, and maintenance. Link
• The role of mechano growth factor in chondrocytes and cartilage defects (2023): Summarizes MGF’s involvement in cartilage repair at macroscopic and cellular levels, including proliferation and anti-apoptosis effects. Link
• Mechano growth factor, a splice variant of IGF-1, promotes neurogenesis by inducing astrocyte proliferation and apoptosis (2017): In vivo study in mice showing MGF enhances hippocampal neurogenesis via astrocyte modulation. Link
• Overexpression of Mechano-Growth Factor Modulates Inflammatory Reaction to Muscle Injury (2018): Examined MGF’s upregulation post-injury and its role in reducing inflammation and promoting regeneration. Link
• Mechano-growth factor peptide, the COOH terminus of unprocessed insulin-like growth factor 1, has independent functions in stimulating myogenesis and proliferation (2014): Highlighted IGF-1-independent effects of MGF on myoblast proliferation and differentiation. Link
GHRP-2 (Growth Hormone Releasing Peptide-2)
GHRP-2 is a synthetic ghrelin mimetic studied for stimulating GH release, appetite, and potential therapeutic uses in GH deficiency. Selected key studies:
• Growth hormone releasing peptide-2 (GHRP-2), like ghrelin, increases food intake in healthy men (2005): Human study confirming GHRP-2’s orexigenic effects similar to ghrelin, with implications for appetite regulation. Link
• Pharmacokinetics and pharmacodynamics of growth hormone-releasing peptide-2 (GHRP-2) in growth-hormone-deficient children (1998): Early pharmacokinetic study supporting its use in pediatric GH therapy via subcutaneous administration. Link
• Growth hormone response to growth hormone-releasing peptide-2 (GHRP-2) in pituitary somatotroph adenoma cells (2012): Investigated direct GH-releasing effects in pituitary cells, independent of GHRH. Link
• Synthetic Growth Hormone-Releasing Peptides (GHRPs): A Historical Appraisal of the Evidences Supporting Their Cytoprotective Effects (2017): Broad review of GHRPs including GHRP-2’s anti-inflammatory and cardioprotective roles in preclinical models. Link
• Robust growth hormone responses to GH-releasing peptide 2 in children with idiopathic short stature (2024): Recent study validating GHRP-2 as a reliable GH provocation test in pediatric populations. Link
Biological Effects and Benefits
Biological Effects and Benefits
In research settings, Four-Time Blend elicits amplified GH/IGF-1 axis activation, leading to enhanced protein synthesis, reduced visceral adiposity, and accelerated myogenic differentiation.
Key effects include increased lean mass accrual (up to 5-10% in rodent models), improved lipid profiles via triglyceride hydrolysis.
Faster wound healing through satellite cell fusion.
Benefits for study include selective appetite modulation (via GHRP-2), targeted abdominal fat reduction (Tesamorelin-driven)
Inflammation-lowering properties (MGF-mediated), with Ipamorelin contributing to cleaner GH pulses for reduced side effect profiles in long-term assays.
Overall, it supports models of anabolic resilience, metabolic optimization, and regenerative medicine, with observed improvements in energy homeostasis and sleep architecture.
Molecular Structure
Four-Time Blend is a lyophilized powder comprising four distinct peptide sequences in equimolar ratios (typically 5 mg GHRP-2, 5 mg Tesamorelin, 500 mcg MGF, 5 mg Ipamorelin per vial for research dosing).
• GHRP-2: A hexapeptide (molecular weight ~818 Da) with sequence His-D-Trp-Ala-Trp-D-Phe-Lys-NH₂, featuring D-amino acids for stability and a C-terminal amide.
• Tesamorelin: A 44-residue linear polypeptide (MW ~5,135 Da), sequence identical to human GHRH(1-44)-NH₂ but with a trans-3-hexenoyl moiety at the N-terminus (Tyr¹) for enhanced half-life and receptor affinity.
• MGF: A 24-amino acid C-terminal fragment (MW ~2,640 Da) from IGF-1Eb, sequence Tyr-Gln-Pro-Ser-Pro-Ser-Thr-Asn-Val-Asp-Lys-Gln-Leu-Arg-Arg-Lys-Val-Arg-Arg (with potential E-peptide extensions), rich in basic residues for myoblast targeting.
• Ipamorelin: A pentapeptide (MW ~711 Da), sequence Aib-His-D-2-Nal-D-Phe-Lys-NH₂, incorporating α-aminoisobutyric acid (Aib) and D-2-naphthylalanine (D-2-Nal) for proteolytic resistance and selectivity.
The blend’s formulation ensures orthogonal stability, with reconstitution in bacteriostatic water yielding a clear solution for experimental use.