Semaglutide (5 mg Vial) Dosage Protocol

Educational guide for reconstitution and weekly dosing of Semaglutide, a GLP-1 receptor agonist studied for metabolic health and body composition.

Quickstart Highlights

5-Amino-1MQ dosage protocols center on this selective, cell-permeable NNMT (Nicotinamide N-methyltransferase) inhibitor studied for its potential to support fat metabolism, preserve lean muscle mass, and elevate intracellular NAD+ levels. By blocking NNMT, 5-Amino-1MQ may help restore cellular energy balance and activate SIRT1 pathways associated with metabolic efficiency.

  • Reconstitute: Add 2.0 mL bacteriostatic water → 2.5 mg/mL concentration
  • Typical weekly range: 0.25–2.4 mg once weekly (subcutaneous)
  • Easy measuring: At 2.5 mg/mL, 1 unit = 0.01 mL = 25 mcg on a U-100 insulin syringe
  • Storage: Lyophilized: freeze at −20 °C (−4 °F); after reconstitution, refrigerate at 2–8 °C (35.6–46.4 °F) and use within 2–4 weeks

Dosing & Reconstitution Guide

Educational guide for reconstitution and daily dosing

Subcutaneous Protocol (2 mL = 2.5 mg/mL)

Phase Daily Dose (mg) Units (per injection) (mL)
Days 1–2 (Tolerance) 2.5 mg once daily 50 units (0.50 mL)
Days 3–4 (Standard) 5 mg once daily 100 units (1.0 mL)
Alternative BID 2.5 mg twice daily 50 units (0.50 mL) × 2

Frequency: Inject once or twice daily subcutaneously. Due to the compound's plasma half-life of approximately 3.8–6.9 hours, twice-daily (BID) dosing may provide more sustained NNMT inhibition. Note: A single 5 mg vial provides approximately 2–3 weekly doses depending on maintenance dose.

Reconstitution Steps

  1. Remove the vial from freezer storage (−20 °C / −4 °F) and allow to equilibrate at room temperature for 15–20 minutes.
  2. Draw 2.0 mL bacteriostatic water with a sterile syringe.
  3. Inject slowly down the vial wall; avoid foaming.
  4. Gently swirl/roll until dissolved—solution should be clear (do not shake).
  5. Label and refrigerate at 2–8 °C (35.6–46.4 °F), protected from light; use within 2–4 weeks.

Biological Action

Semaglutide represents a synthetic GLP-1 receptor agonist that mimics the effects of glucagon-like peptide-1, a naturally occurring incretin hormone.

As a long-acting GLP-1 analog, Semaglutide binds to GLP-1 receptors to enhance insulin secretion, suppress glucagon release, and promote satiety through delayed gastric emptying.

Semaglutide has been extensively studied for its effects on glycemic control, weight management, and metabolic health in clinical settings.

Potential Benefits & Side Effects

Findings from endocrinology and metabolic research.

Injection Technique

General subcutaneous guidance from clinical best-practice resources.

  1. Clean the vial stopper and skin with alcohol; allow to dry.
  2. Pinch a skinfold; insert the needle at 45–90° into subcutaneous tissue.
  3. Do not aspirate for subcutaneous injections; inject slowly and steadily.
  4. Rotate sites systematically (abdomen, thighs, upper arms) to avoid lipohypertrophy.
  5. Slow injection may minimize any stinging sensation associated with the compound.

Important Notes

Practical considerations for consistency and safety.

Important Disclaimer: This content is intended for educational purposes only and does not constitute medical advice, diagnosis, or treatment. This is not medical advice and is for informational purposes only. Always consult with a qualified healthcare professional before starting any new research protocol.

References

Nature Medicine (2014)
Nicotinamide N-methyltransferase knockdown protects against diet-induced obesity View Source
PMC (2024)
Nicotinamide N-methyltransferase inhibition mitigates obesity-related metabolic dysfunctions View Source
Frontiers in Pharmacology (2024)
NNMT: a novel therapeutic target for metabolic syndrome View Source