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

5-Amino-1MQvsProstamax

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-MechanisticHUMAN-REVIEWED11/38 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
Prostamax
Khavinson Bioregulator · Tissue-Specific Peptide
0.05 ng/mLActive concentrationZakutskiĭ 2006
2.5×SCE frequency increaseDzhokhadze 2012
4 AAPeptide length
SQ · Protocol per Khavinson tradition

01Mechanism of Action

Parameter
5-Amino-1MQ
Prostamax
Primary target
Nicotinamide N-methyltransferase (NNMT)Neelakantan 2018
Chromatin in prostatic cells — pericentromeric heterochromatin regions
Pathway
NNMT inhibition → preserved cellular SAM + NAD⁺ → restored methylation balance + ↑ thermogenic gene expressionNeelakantan 2018
Epigenetic modulation → heterochromatin decondensation → transcriptional derepressionDzhokhadze 2012
Downstream effect
Reversal of HFD-induced obesity in murine models; improved metabolic profileNeelakantan 2018
Increased sister chromatid exchange, Ag-NOR activation, reduced C-heterochromatin condensation; tissue-specific regenerative stimulation in prostate organotypic culturesDzhokhadze 2012Zakutskiĭ 2006
Feedback intact?
Origin
Selective small-molecule inhibitor designed in academic medicinal chemistry programsNeelakantan 2018
Synthetic tetrapeptide modeled on naturally occurring protein-derived bioregulators isolated between lysine-arginine motifs in long-lived speciesKhavinson 2017
Antibody development

02Dosage Protocols

Parameter
5-Amino-1MQ
Prostamax
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 / organotypic cultureZakutskiĭ 2006Dzhokhadze 2012
No randomized controlled trials in humans.
Duration
8–12 weeks per cycle
Not specified
Khavinson protocols typically 10–20 days per cycle; no long-term safety data.
Form
Oral capsule
Timing
Morning fasted preferred
Half-life
Hours (estimated; no human PK published)
Effective concentration (in vitro)
0.05 ng/mLZakutskiĭ 2006
Organotypic culture model; demonstrated tissue-specific stimulation.
Human clinical dose
Not established
No published human trials; dosing extrapolated from Russian clinical tradition (not peer-reviewed).
Age groups studied
Young (3-week) and aged (18-month) rats; elderly humans (75–86 years) in vitroZakutskiĭ 2006Dzhokhadze 2012

04Side Effects & Safety

Parameter
5-Amino-1MQ
Prostamax
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
Published adverse events
None reported in available literature
Genotoxicity signals
Increased sister chromatid exchange (SCE) — marker of DNA recombination/repair; unclear long-term implications
Metal ion interactions
Modulates Cu(II) and Cd(II) chromatin effects; unknown clinical relevance
Human safety data
Absent — no published Phase 1/2/3 trials
Absolute Contraindications
5-Amino-1MQ
  • ·Pregnancy / breastfeeding
  • ·Active malignancy
Prostamax
  • ·Active prostate malignancy — epigenetic modulation effects unknown in cancer
Relative Contraindications
5-Amino-1MQ
  • ·Methylation-sensitive conditions (MTHFR mutation)
  • ·Concurrent niacin / NAD+ precursor supplementation (theoretical interference)
Prostamax
  • ·History of prostate cancer — theoretical concern re: transcriptional activation
  • ·Undiagnosed prostatic nodules or elevated PSA

05Administration Protocol

Parameter
5-Amino-1MQ
Prostamax
1. Form
Oral capsule. No injection.
Subcutaneous or intramuscular — per Khavinson bioregulator tradition. No published human pharmacokinetic data.
2. Administration
Take with water, fasted preferred.
If lyophilised: reconstitute with sterile water per manufacturer protocol (not standardized in literature).
3. Timing
Morning fasted.
Typically daily or every-other-day in Russian clinical tradition; duration 10–20 days per cycle.
4. Storage
Room temp ≤25 °C, dry place.
No established biomarkers. Theoretical: PSA, prostate imaging, symptom scores (IPSS for BPH).
5. Caveat
Monitor B-vitamin status with chronic use.
All protocols derived from non-peer-reviewed Russian clinical practice; Western regulatory approval absent.