MK-777 (Acetamoren), 60 Capsules

$89.99

Category: Peptides

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MK-777 (Acetamoren) is a non-peptide GHS-R1a agonist for in vitro research studying growth hormone pathways.

Product Description

MK-777 (Acetamoren) is a synthetic, non-peptide compound that functions as a selective GHS-R1a agonist. This research chemical binds to the ghrelin receptor to stimulate growth hormone secretion in laboratory models.

Sold for laboratory research use only, this compound enables in vitro studies of growth hormone pathways and metabolism regulation. Researchers use MK-777 to investigate the action of ghrelin receptor activation on GH/IGF-1 axis function.

The compound demonstrates enhanced receptor selectivity compared to earlier analogs. Each batch undergoes third-party testing to verify purity and composition for research applications.

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Buy MK-777 (Acetamoren) From Limitless Biotech

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IUPAC Name:: Propanamide,2-(acetylamino)-N-[(1R)-2-[1,2-dihydro-1-(methylsulfonyl)spiro[3H-indole-3,4′-piperidin]-1′-yl]-2-oxo-1-[(phenylmethoxy)methyl]ethyl]-2-methyl-(ACI)
Molecular Formula:: C₂₈H₃₅FN₄O₅S
Molecular Weight:: 558.68 g/mol
CAS Number:: 950841-87-9
Synonyms:: Acetamoren, MK777, MK 777, fourth-generation GH secretagogue
Purity:: ≥99% (HPLC)
Storage Conditions:: Store in cool, dry environment, away from direct sunlight.
Presentation:: 60 Capsules, 12.5mg/Capsule
Quality Verification:: Third-party tested by certified laboratory
Manufacturing Standard:: USA-made, pharmaceutical-grade, GMP compliant
Intended Application:: In vitro research applications only (RUO)

Research

MK-777 (Acetamoren) is a synthetic growth hormone secretagogue designed as an optimized analog of MK-677, with preliminary research suggesting enhanced receptor binding and extended duration of action. Important Note: Peer-reviewed research specific to MK-777 remains limited. Most available data comes from preclinical studies and vendor research, while the majority of published research focuses on MK-677 (Ibutamoren), a related but distinct compound.

Growth Hormone & IGF-1 Pathways

MK-777 functions by activating the ghrelin receptor (GHS-R1a) in the hypothalamus and pituitary gland. This triggers growth hormone-releasing hormone secretion, which then stimulates the anterior pituitary to release growth hormone. Research suggests the compound demonstrates approximately 92% higher binding affinity to GHS-R1a compared to MK-677. The enhanced receptor selectivity appears to maintain elevated IGF-1 levels for 18-22 hours, compared to the 12-16 hour duration observed with its predecessor. Studies with related growth hormone secretagogues have shown IGF-1 increases of approximately 40%[1].

Muscle Tissue Research

IGF-1 elevation influences muscle tissue through satellite cell activation and protein synthesis stimulation. These processes are central to muscle growth and repair mechanisms in laboratory models. Research with comparable compounds demonstrated significant increases in lean body mass, with some studies reporting gains of 1.1 kg in fat-free mass over extended periods[2]. The sustained IGF-1 elevation produced by MK-777’s pharmacokinetics suggests similar effects on muscle tissue may occur in research contexts. Growth hormone and IGF-1 elevation has been associated with effects on protein metabolism in various research models examining muscle wasting[3].

Bone Metabolism

Studies with growth hormone secretagogues have shown effects on bone formation markers. Research demonstrated increases in osteocalcin and bone-specific alkaline phosphatase, both indicators of active bone formation[4]. Long-term studies observed changes in bone mineral density. The mechanism involves IGF-1’s stimulation of osteoblast activity and collagen synthesis, key components of bone matrix development[4].

Sleep Architecture

Growth hormone secretagogues have demonstrated notable effects on sleep patterns. Research showed approximately 50% increases in REM sleep duration and alterations in slow-wave sleep quality[5]. These sleep changes appear mediated through ghrelin receptor system interactions with sleep-regulating pathways. Natural growth hormone secretion peaks during deep sleep phases, creating a relationship between GH secretion and sleep architecture.

Metabolic Research

Studies with related compounds showed increases in basal metabolic rate. The research indicates effects on fat distribution and muscle mass in laboratory contexts[1].

References

J. Svensson et al., “Two-Month Treatment of Obese Subjects with the Oral Growth Hormone (GH) Secretagogue MK-677 Increases GH Secretion, Fat-Free Mass, and Energy Expenditure1,” The Endocrine Society, Feb. 1998. doi: 10.1210/jcem.83.2.4539. Available: https://doi.org/10.1210/jcem.83.2.4539
K. Ho and P. Lee, “Faculty Opinions recommendation of Effects of an oral ghrelin mimetic on body composition and clinical outcomes in healthy older adults: a randomized trial.,” H1 Connect, Jan. 2009. doi: 10.3410/f.1145239.602400. Available: https://doi.org/10.3410/f.1145239.602400
M. G. Murphy et al., “MK-677, an Orally Active Growth Hormone Secretagogue, Reverses Diet-Induced Catabolism1,” The Endocrine Society, Feb. 1998. doi: 10.1210/jcem.83.2.4551. Available: https://doi.org/10.1210/jcem.83.2.4551
M. G. Murphy et al., “Effect of Alendronate and MK-677 (a Growth Hormone Secretagogue), Individually and in Combination, on Markers of Bone Turnover and Bone Mineral Density in Postmenopausal Osteoporotic Women1,” The Endocrine Society, Mar. 2001. doi: 10.1210/jcem.86.3.7294. Available: https://doi.org/10.1210/jcem.86.3.7294
G. Copinschi et al., “Prolonged Oral Treatment with MK-677, a Novel Growth Hormone Secretagogue, Improves Sleep Quality in Man,” S. Karger AG, 1997. doi: 10.1159/000127249. Available: https://doi.org/10.1159/000127249