Side-by-side · Research reference
5-Amino-1MQvsCJC-1295 (no DAC)
Side-by-side comparison across mechanism, dosage, evidence, side effects, administration, and stack synergies. Citations on every claim where available.
AAnimal-StrongDraft8/38 cited
BPhase 1Reviewed15/51 cited
5-Amino-1MQ
NNMT inhibitor · Methylation / SAM modulation
Oral · Once daily fasted
CJC-1295 (no DAC)
Short-acting GHRH · No DAC variant
SQ · Pre-sleep · 1–2×/day
01Mechanism of Action
Parameter
5-Amino-1MQ
CJC-1295 (no DAC)
Primary target
Nicotinamide N-methyltransferase (NNMT)Neelakantan 2018
Pituitary GHRH receptorTeichman 2006
Pathway
NNMT inhibition → preserved cellular SAM + NAD⁺ → restored methylation balance + ↑ thermogenic gene expressionNeelakantan 2018
GHRH-R → Gαs → cAMP → PKA → GH vesicle exocytosisTeichman 2006
Downstream effect
Reversal of HFD-induced obesity in murine models; improved metabolic profileNeelakantan 2018
Pulsatile GH release matching physiological pattern; subsequent IGF-1 elevationIonescu 2006
Origin
Selective small-molecule inhibitor designed in academic medicinal chemistry programsNeelakantan 2018
Modified human GRF 1-29 with four substitutions (D-Ala²/Gln⁸/Ala¹⁵/Leu²⁷) for protease resistanceTeichman 2006
Antibody development
—
Not reported in short-term studies
02Dosage Protocols
Parameter
5-Amino-1MQ
CJC-1295 (no DAC)
Standard dose
100–200 mg / day oralNeelakantan 2018
Anecdotal community range; murine doses scaled.
100 mcg per injectionTeichman 2006
Often paired with ipamorelin in same syringe.
Frequency
Once daily, fasted
1–2× daily (pre-sleep ± morning)
Lower / starter dose
50 mg / day
50 mcg per dose
Evidence basis
Animal-strong; no human RCT dataNeelakantan 2018
Phase 1 (CJC-1295 with DAC); analog dataTeichman 2006Ionescu 2006
No-DAC variant is less studied directly; PK extrapolated from native GHRH.
Duration
8–12 weeks per cycle
8–12 weeks on / 4 off (anecdotal)
Form
Oral capsule
—
Timing
Morning fasted preferred
Pre-sleep + fasted preferred
Half-life
Hours (estimated; no human PK published)
~30 minIonescu 2006
Short pulse vs CJC-1295-DAC (~8 days). Choose no-DAC for pulsatile, DAC for sustained.
Reconstitution
—
Bacteriostatic water
04Side Effects & Safety
Parameter
5-Amino-1MQ
CJC-1295 (no DAC)
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
Contraindicated in active malignancy (GH/IGF-1 axis)
Pregnancy / OB
Avoid
Avoid
Drug interactions
Theoretical with niacin / B-vitamin supplements
—
Injection site reaction
—
Erythema, mild pruritus
Flushing / headache
—
Common transient effect
Cortisol elevation
—
Minimal at standard doses
Prolactin elevation
—
Minimal
Glucose intolerance
—
Possible at high cumulative doses
IGF-1 elevation
—
Dose-dependent; monitor with chronic use
Absolute Contraindications
5-Amino-1MQ
- ·Pregnancy / breastfeeding
- ·Active malignancy
CJC-1295 (no DAC)
- ·Active malignancy or cancer history
- ·Pregnancy / breastfeeding
- ·Disrupted hypothalamic-pituitary axis
Relative Contraindications
5-Amino-1MQ
- ·Methylation-sensitive conditions (MTHFR mutation)
- ·Concurrent niacin / NAD+ precursor supplementation (theoretical interference)
CJC-1295 (no DAC)
- ·Untreated diabetes
- ·Severe insulin resistance
05Administration Protocol
Parameter
5-Amino-1MQ
CJC-1295 (no DAC)
1. Form
Oral capsule. No injection.
Add 2 mL bacteriostatic water to 2 mg vial → 1 mg/mL = 100 mcg per 0.1 mL. Roll gently.
2. Administration
Take with water, fasted preferred.
Subcutaneous, abdomen or thigh. Rotate sites.
3. Timing
Morning fasted.
Pre-sleep preferred. Often combined with ipamorelin in the same syringe.
4. Storage
Room temp ≤25 °C, dry place.
Lyophilised: room temp, protected from light. Reconstituted: refrigerate 2–8 °C, use within 30 days.
5. Caveat
Monitor B-vitamin status with chronic use.
29–31G, 4–8 mm insulin syringe.
06Stack Synergy
5-Amino-1MQ
— no documented stacks
CJC-1295 (no DAC)
+ Ipamorelin
StrongCJC-1295 (no DAC) and ipamorelin are the canonical "GHRH + GHRP" dual-axis stack at physiological timing. Both peak within 30 min and clear within 2 hours, producing a sharp, high-amplitude GH pulse closely resembling natural physiology. Preferred over the CJC-1295-DAC + ipamorelin stack when pulsatility (vs sustained elevation) is the goal.
- CJC-1295 (no DAC)
- 100 mcg SQ · pre-sleep
- Ipamorelin
- 200–300 mcg SQ · same injection
- Primary benefit
- Pulsatile GH stimulation, recovery, body composition