5-Amino-1MQ
NNMT inhibitor · Small molecule
A peptide-adjacent small molecule studied in metabolic and adipocyte models rather than a peptide.
Mechanism
Experimental nicotinamide N-methyltransferase inhibition
Protocol studied in research
Study design shown in plain language. This is not a personal dosing recommendation.
Human evidence is absent, limited or not confirmatory
Anecdotal schedules are excluded because frequency of online repetition does not establish identity, safety, or a clinically meaningful dose.
Community-Reported Research Schedules
Descriptive community patterns are separated from clearly labeled trial-derived reference rows. Neither is personal dosing guidance.
| Research context or phase | Amount per administration | Schedule total | Frequency | Timing | Administration | Evidence level |
|---|---|---|---|---|---|---|
| Common oral research schedule | 50–150 mg | 50–150 mg/day | Once daily or divided | Morning through midday | Oral | Community-reported |
| Community subcutaneous range | 2.5–5 mg | 2.5–5 mg/day | Usually once daily; sometimes divided | Morning or morning-to-midday | Subcutaneous | Community-reported |
Important: Repetition in online communities does not establish product identity, safety, effectiveness, or an appropriate exposure. Route-specific schedules, half-life estimates and reported cycle lengths are shown for comparison only.
Example Reconstitution Protocol
A hypothetical concentration calculation for literacy and review—not preparation, administration, or dosing instructions.
At this concentration, the upper 5 mg community amount equals 0.50 mL or 50 U-100 units.
Values are rounded: 2.5 mg equals 0.15 mL (15 units); 5 mg equals 0.30 mL (30 units).
Important: Vial strength, diluent identity, compatibility, sterility, stability and beyond-use time are product-specific. Never infer them from this arithmetic example. Use manufacturer, pharmacy, study, or licensed-clinician instructions for an actual preparation.
Cycle & Supplies Planning
Phase-by-phase cycle math showing how long a vial lasts and the estimated supplies required.
Cycle Structure
| Phase | Amount | Frequency | Weekly total |
|---|---|---|---|
| Selected planning schedule | 2.5–5 mg | Usually once daily; sometimes divided | 17.5–35 mg/week |
Peptide Vials
| Cycle | Total compound | Vials needed | How long one vial lasts |
|---|---|---|---|
| 4 weeks | 70–140 mg | 7–14 × 10 mg | 2–4 administrations |
| 8 weeks | 140–280 mg | 14–28 × 10 mg | 2–4 administrations |
| 12 weeks | 210–420 mg | 21–42 × 10 mg | 2–4 administrations |
Bacteriostatic Water
| Cycle | Total water used | 10 mL bottles needed |
|---|---|---|
| 4 weeks | 7–14 mL | 1–2 × 10 mL |
| 8 weeks | 14–28 mL | 2–3 × 10 mL |
| 12 weeks | 21–42 mL | 3–5 × 10 mL |
Insulin Syringes (U-100)
| Cycle | Administrations | Syringes needed |
|---|---|---|
| 4 weeks | 28 | 28 |
| 8 weeks | 56 | 56 |
| 12 weeks | 84 | 84 |
Ranges reflect the low and high ends of the displayed community schedule. Vials and 10 mL water bottles are rounded up; one new U-100 syringe is counted per subcutaneous administration.
Planning boundary: These are arithmetic examples based on the displayed research schedule—not personal dosing or purchasing instructions. Confirm product format, compatibility, route, sterility, storage, and discard timing independently. U-100 units measure liquid volume, not potency.
Safety signal
No validated therapeutic exposure or long-term human safety profile has been established.
Reported doses describe either a specific study or an unverified community pattern. Neither is personal medical guidance.