5-amino-1MQ dosage: reported doses and schedule
An experimental NNMT blocker with animal findings, no human dosing trials and uncertain risks.
Also called: 5-Amino-1MQ, 5-amino-1-methylquinolinium, 5A1MQ, 5-AMQ, 5A-1MQ, 5-amino-1-methylquinolinium iodide, 5-amino-1-methylquinolinium chloride.
NNMT inhibitors · Small-molecule nicotinamide N-methyltransferase inhibitor · Evidence: Animal studies only.
Typical reported dose: 25 mg twice a day by mouth (50 mg a day)
- Oral 50 mg, split twice: 25 mg morning and 25 mg early afternoon twice daily; 50 mg total per day, by mouth. Reported by users, common report. Studied in: Adults in online community reports; product contents and outcomes unverified. (source)
- Oral guide: 50 then 75 mg: 50 mg daily for 1–2 weeks, then 75 mg daily if increased once daily, by mouth. Reported by users, occasional report. Studied in: Adults in online community reports; product contents and outcomes unverified. (source)
- Small injections: 500–1000 mcg: 500–1000 mcg under the skin daily once daily, under the skin. Reported by users, occasional report. Studied in: Adults in online community reports; product contents and outcomes unverified. (source)
- Daily 5 mg report: 5 mg under the skin each morning once daily in the morning, under the skin. Reported by users, occasional report. Studied in: Adults in online community reports; product contents and outcomes unverified. (source)
- Injection guide: 10–30 mg: 10–30 mg under the skin daily once daily, under the skin. Reported by users, occasional report. Studied in: Adults in online community reports; product contents and outcomes unverified. (source)
- High injection report: 100 mg: 100 mg under the skin daily once daily, under the skin. Reported by users, rare report. Studied in: Adults in online community reports; product contents and outcomes unverified. (source)
These are doses reported in labels, trials or user reports, not a personal plan. Check the source behind each one.
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Sources
- 21 CFR 216.23 — Bulk drug substances that can be used to compound drug products in accordance with section 503A of the Federal Food, Drug, and Cosmetic Act., Office of the Federal Register · eCFR · 2026
- Bulk Drug Substances Nominated for Use in Compounding Under Section 503A of the Federal Food, Drug, and Cosmetic Act, FDA · FDA · 2026
- GenoGenix LLC - 718739 - 01/20/2026, FDA · FDA · 2026
- July 23-24, 2026: Meeting of the Pharmacy Compounding Advisory Committee - 07/23/2026, FDA · FDA · 2026
- Medicines, European Medicines Agency · European Medicines Agency · 2026
- MHRA Products | Home, MHRA · MHRA · 2026
- Pyrogen and Endotoxins Testing: Questions and Answers, FDA · 2026
- The 2026 Prohibited List, World Anti-Doping Agency · WADA · 2026
- Therapeutic Goods (Poisons Standard—October 2026) Instrument 2026, Australian Government · Australian Government · 2026
- Q6A Specifications: Test Procedures and Acceptance Criteria for New Drug Substances and New Drug Products: Chemical Substances, FDA · FDA · 2000
- Australian Register of Therapeutic Goods (ARTG), Therapeutic Goods Administration · TGA
- Drug Product Database: Access the database, Health Canada · Health Canada
- Poisoning, MedlinePlus / US National Library of Medicine
- Rhabdomyolysis, MedlinePlus / US National Library of Medicine
- Clinical Pharmacology & Toxicology Pearl of the Week ~ Unauthorized Injectable Peptides ~, University of Calgary Clinical Pharmacology & Toxicology · 2026
Sources checked: 2026-10-18.
Information only, not medical advice. Peptifacts does not sell anything and does not link to sellers.