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Specimen Atlas of Research Peptides81 plates · MIT
Side-by-side · Research reference

HGH Fragment 176-191vsPinealon

Side-by-side comparison across mechanism, dosage, evidence, side effects, administration, and stack synergies. Citations on every claim where available.

AAnimal-StrongHUMAN-REVIEWED28/59 cited
BHuman-MechanisticAUTO-DRAFTED12/36 cited
HGH Fragment 176-191
GH Fragment · Pre-Clinical
50%Weight gain reductionNg 2000
~26 minHalf-life (est.)
No IGF-1 ↑GH axis impact
SQ · IP (animal) · Oral (tested)
Pinealon
Pineal-derived · Neuroprotective
5–10 mgPer cycle doseKhavinson 2014
HumanMechanisticKhavinson 2014
HoursHalf-life (est)
SQ or IM · Daily for 10 days · 1-2×/year

01Mechanism of Action

Parameter
HGH Fragment 176-191
Pinealon
Primary target
Beta-3 adrenergic receptors on adipocytesHeffernan 2001
Antioxidant defense + neuronal gene expression (proposed)Khavinson 2014
Pathway
Fragment → β3-AR upregulation → Enhanced lipolytic sensitivityHeffernan 2001
Modulation of antioxidant enzymes (SOD, catalase) + neurotrophic factor expressionKhavinson 2014
Downstream effect
Increased lipolysis and beta-3 AR mRNA expression without IGF-1 axis activation
Reduced oxidative stress in neurons; improved cognitive function in age-related declineKhavinson 2014
Feedback intact?
N/A — does not interact with GH/IGF-1 axis
Origin
Synthetic peptide derived from hGH residues 176-191; AOD9604 includes N-terminal tyrosine (177-191)Cox 2015
Synthetic 4-AA peptide derived from pineal gland extractKhavinson 2014
Antibody development
Not reported in available studies

02Dosage Protocols

Parameter
HGH Fragment 176-191
Pinealon
Animal dose (oral)
500 mcg/kg body weightNg 2000
Obese Zucker rats, 19 days.
Animal dose (IP)
Not specified (14-day chronic administration)Heffernan 2001
Obese mice, daily IP injection.
Human equivalent dose
Not established — no published human RCTs
Frequency
Once daily (animal models)
Once daily during cycle
Evidence basis
Animal studies only
Russian clinical trials + in vitroKhavinson 2014
Duration tested
Detection window
50 pg/mL LOD in urine; stable metabolite extends detectionCox 2015
WADA-banned; anti-doping testing available.
Oral bioavailability
Demonstrated efficacy in animal oral administrationNg 2000
Potential for oral therapeutic development.
Standard dose
5–10 mg / day for 10 daysKhavinson 2014
Lower / starter dose
2.5 mg / day
Duration
10-day cycles, 1–2× per year
Reconstitution
Bacteriostatic water
Timing
No specific time
Half-life
Hours

03Metabolic / Fat Loss Evidence

Parameter
HGH Fragment 176-191
Pinealon
Primary fat target
Adipose tissue (general) — beta-3 AR mediated lipolysisHeffernan 2001
Weight gain reduction
50% reduction vs control (15.8 ± 0.6 g vs 35.6 ± 0.8 g)Ng 2000
Obese Zucker rats, 19 days oral administration.
Body fat reduction
Significant decrease in body weight and body fat in obese mice (14 days)Heffernan 2001
Lipolytic activity
Increased adipose tissue lipolytic activityNg 2000
Direct measurement in treated animals.
Beta-3 AR expression
Upregulated β3-AR mRNA in obese mice to lean-comparable levelsHeffernan 2001
Insulin sensitivity
No adverse effect — euglycemic clamp confirmedNg 2000
Contrasts with intact hGH diabetogenic effects.
IGF-1 impact
No elevation — fragment does not activate GH/IGF-1 axis
Beta-3 AR dependency
Effect abolished in β3-AR knockout miceHeffernan 2001
Confirms β3-AR as primary mechanism.
Route of administration
Efficacy demonstrated via oral and IP routesNg 2000Heffernan 2001
Human evidence
None published — pre-clinical only

04Side Effects & Safety

Parameter
HGH Fragment 176-191
Pinealon
Insulin sensitivity
No adverse effects observed in euglycemic clamp (animal)Ng 2000
GH/IGF-1 axis
No activation — avoids diabetogenic effects of full GHNg 2000
Human safety data
Not available — no published human trials
WADA status
Banned as performance-enhancing drugCox 2015
Metabolic profile
Six metabolites identified; CRSVEGSCG most stableCox 2015
Detection window implications for doping control.
Injection site reaction
Mild irritation
Long-term safety
Limited Western data
Pregnancy / OB
Avoid
Absolute Contraindications
HGH Fragment 176-191
  • ·Competitive athletes (WADA-banned)Cox 2015
Pinealon
  • ·Pregnancy / breastfeeding
Relative Contraindications
HGH Fragment 176-191
  • ·Absence of human safety data — experimental use only
Pinealon
  • ·Active malignancy (theoretical via gene expression modulation)

05Administration Protocol

Parameter
HGH Fragment 176-191
Pinealon
1. Route
Subcutaneous injection primary route in research context. Oral administration demonstrated efficacy in animal models at 500 mcg/kg.
Add 1–2 mL bacteriostatic water to 10 mg vial.
2. Frequency
Once daily dosing used in animal studies. Timing not specified; GH-independent mechanism suggests flexibility.
SQ — abdomen preferred.
3. Duration
Animal protocols: 14–19 days. Human duration not established — no published trials.
Daily during cycle, any time.
4. Storage
Lyophilized peptide storage per standard peptide protocols. Metabolite stability suggests refrigerated reconstituted solution viable.
Lyophilised: room temp. Reconstituted: refrigerate ≤30 days.
5. Detection
Detectable in urine via SPE-LC-MS at 50 pg/mL LOD. Extended detection window via stable metabolite CRSVEGSCG.Cox 2015
29–31G, 4–8 mm insulin syringe.

06Stack Synergy

HGH Fragment 176-191
— no documented stacks
Pinealon
+ Epitalon
Moderate
View Epitalon

Pinealon (neuroprotection) + Epitalon (telomerase activation) form the canonical Khavinson "longevity stack" — both pineal-derived bioregulators with complementary axes. Pinealon supports neuronal antioxidant defense; Epitalon supports telomere maintenance. Anecdotally cycled together 1–2× per year.

Pinealon
5–10 mg SQ · daily × 10 days
Epitalon
5–10 mg SQ · daily × 10 days (overlap or alternate)
Primary benefit
Neuroprotection + telomere preservation