MK-677 Capsules (25mg) 60 Count

  • Oral GH Secretagogue: Non-peptide ghrelin mimetic (C₂₇H₃₆N₄O₅S), >60% bioavailability
  • GHS-R1a Agonist: High affinity (pKi = 8.14, EC50 = 1.3 nM), sustained GH-IGF-1 elevation
  • Clinical Evidence: 30-year history, >1,000 subjects, Phase 3 development for pediatric GHD
Manufacturer: RiboCore
Availability: In stock
SKU: RC-MK-677-CAPSULES-25MG
$99.00
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Technical Specifications

CharacteristicValue
CAS Number159634-47-6
Molecular Weight528.66 Da
Molecular FormulaC₂₇H₃₆N₄O₅S
ClassNon-peptide growth hormone secretagogue
Purity≥98% (HPLC)
FormCapsules (25mg)

MK-677 (ibutamoren, MK-0677, L-163,191, LUM-201) is a potent, orally active, non-peptide growth hormone secretagogue that selectively agonizes the GHS-R1a (ghrelin receptor). First developed by Merck & Co. in the mid-1990s, MK-677 has been extensively studied in over 1,000 subjects across randomized controlled trials spanning nearly three decades. Unlike peptide-based GH secretagogues requiring injection, MK-677 demonstrates oral bioavailability exceeding 60% and a prolonged half-life enabling once-daily dosing.

MK-677 features a unique spirocyclic architecture linking an indoline ring system to a piperidine moiety. Cryo-EM structural analysis at 2.7 Å resolution revealed that ibutamoren binding induces conformational changes through an E124-R283 salt bridge mechanism and W276 toggle switch, enabling G protein coupling and downstream GH release.

Key Research Highlights

Research AreaKey Finding
Elderly GH Restoration25 mg daily increased GH by 97% and restored IGF-1 from 141 to 265 μg/L in adults ages 64-81 (Chapman et al., 1996)
Body Composition2-year trial: fat-free mass +1.1 kg vs. -0.5 kg placebo (P < 0.001); LDL -5.4 mg/dL; sustained without tachyphylaxis (Nass et al., 2008)
Nitrogen BalanceReversed diet-induced catabolism: +0.31 g/day vs. -1.48 g/day placebo (P < 0.01) in calorie-restricted subjects (Murphy et al., 1998)
Sleep Quality~50% increase in stage IV sleep and >20% increase in REM sleep; deviations from normal sleep decreased from 42% to 8% (Copinschi et al., 1997)
Pediatric GHDPhase 2 (LUM-201): 8.0 cm/year height velocity; 62% GH increase, 80% IGF-1 increase at 6 months; Phase 3 planned
NeuroprotectionReduced amyloid beta to 30% of controls, decreased neuroinflammation in 5XFAD mice (Jeong et al., 2018)

Research Applications

  • Growth hormone-IGF-1 axis research and somatopause
  • Pediatric growth hormone deficiency (Phase 3 development)
  • Body composition and lean mass preservation in elderly
  • Bone metabolism and osteoporosis research
  • Sleep physiology and architecture modulation
  • Catabolic disease states and nitrogen balance
  • Neuroprotection and Alzheimer's disease models
  • Ghrelin receptor pharmacology and structural biology
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