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

5-Amino-1MQvsLivagen

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

AAnimal-StrongAUTO-DRAFTED8/38 cited
BAnimal-StrongHUMAN-REVIEWED20/32 cited
5-Amino-1MQ
NNMT inhibitor · Methylation / SAM modulation
100–200 mgDaily dose (oral)Neelakantan 2018
AnimalEvidence levelNeelakantan 2018
HoursHalf-life (est)
Oral · Once daily fasted
Livagen
Khavinson Bioregulator · Hepatoprotective Tetrapeptide
50%Dipeptidase inhibitionTimofeeva 2005
Oral / SQRoutes tested
LiverTarget tissueKhavinson 2001
Oral or SQ · Tissue-specific to liver

01Mechanism of Action

Parameter
5-Amino-1MQ
Livagen
Primary target
Nicotinamide N-methyltransferase (NNMT)Neelakantan 2018
Hepatocyte protein synthesis machineryBrodskiĭ 2001
Pathway
NNMT inhibition → preserved cellular SAM + NAD⁺ → restored methylation balance + ↑ thermogenic gene expressionNeelakantan 2018
Tissue-specific bioregulator → Hepatocyte stimulation → Protein synthesis normalizationBrodskiĭ 2001Khavinson 2001
Downstream effect
Reversal of HFD-induced obesity in murine models; improved metabolic profileNeelakantan 2018
Age-dependent enzyme normalization, hepatoprotection in fibrosis/hepatitis models, elevated protein synthesis in senescent hepatocytes
Feedback intact?
Origin
Selective small-molecule inhibitor designed in academic medicinal chemistry programsNeelakantan 2018
Directed chemical synthesis from amino acid analysis of liver polypeptide preparations (Ventvil)
Antibody development

02Dosage Protocols

Parameter
5-Amino-1MQ
Livagen
Standard dose
100–200 mg / day oralNeelakantan 2018
Anecdotal community range; murine doses scaled.
Frequency
Once daily, fasted
Lower / starter dose
50 mg / day
Evidence basis
Animal-strong; no human RCT dataNeelakantan 2018
Animal models (rats, 1–24 months age); in vitro hepatocyte cultureTimofeeva 2005Brodskiĭ 2001Khavinson 2002
Duration
8–12 weeks per cycle
Form
Oral capsule
Timing
Morning fasted preferred
Half-life
Hours (estimated; no human PK published)
Animal dose (oral)
Not specified in abstracts; 2-week administration protocolTimofeeva 2005
Per os administration in rats.
Duration (experimental)
2 weeks (enzyme study); up to 24 months (cell culture)Timofeeva 2005Brodskiĭ 2001
Route
Oral or subcutaneous
Resists peptidase hydrolysis, enabling oral bioavailability.Timofeeva 2005
Human data
None in provided literature

04Side Effects & Safety

Parameter
5-Amino-1MQ
Livagen
GI symptoms
Mild nausea (anecdotal)
Methylation disruption
Theoretical risk if NNMT is over-inhibited (B vitamin metabolism)
Long-term safety
Unknown — no human trials
Cancer risk
Unclear — NNMT also studied in oncology contexts
Pregnancy / OB
Avoid
Drug interactions
Theoretical with niacin / B-vitamin supplements
Reported adverse effects
None documented in animal studies
Human safety data
No human trials in provided literature
Peptide hydrolysis
Weakly hydrolyzed; minimal breakdown by intestinal enzymesTimofeeva 2005
Absolute Contraindications
5-Amino-1MQ
  • ·Pregnancy / breastfeeding
  • ·Active malignancy
Livagen
Relative Contraindications
5-Amino-1MQ
  • ·Methylation-sensitive conditions (MTHFR mutation)
  • ·Concurrent niacin / NAD+ precursor supplementation (theoretical interference)
Livagen

05Administration Protocol

Parameter
5-Amino-1MQ
Livagen
1. Form
Oral capsule. No injection.
Oral administration supported by peptidase resistance. Subcutaneous route used in organotypic culture experiments.Timofeeva 2005Khavinson 2001
2. Administration
Take with water, fasted preferred.
No specific timing documented. Two-week protocols used in animal models with daily administration.Timofeeva 2005
3. Timing
Morning fasted.
Elderly individuals may exhibit different enzyme normalization patterns than younger cohorts, based on rat age-stratified findings.Timofeeva 2005
4. Storage
Room temp ≤25 °C, dry place.
5. Caveat
Monitor B-vitamin status with chronic use.