NAD+ / MOTS-c / 5-Amino-1MQBlend
NAD+ + MOTS-c + 5-Amino-1MQ metabolic & longevity blend.
- Status
- Research / not approved
- Developer
- Compounded research blend; vendor-specific
- Receptors / target
- Not a single target — combines NAD+ (redox coenzyme), MOTS-c (mitochondrial-derived peptide) and 5-Amino-1MQ (NNMT inhibitor); all converge on cellular and mitochondrial energy metabolism
- FDA-approved?
- NO
- Prescription available?
- NO
- Studied for
- cellular & mitochondrial metabolismNAD+ / energy metabolismmetabolic regulation / insulin sensitivityaging / longevity research
Overview
NAD+ / MOTS-c / 5-Amino-1MQ is a compounded metabolic / longevity research blend combining three agents that converge on cellular and mitochondrial energy metabolism: the redox coenzyme NAD+, the mitochondrial-derived peptide MOTS-c, and the NNMT inhibitor 5-Amino-1MQ (which is a small molecule, not a peptide). It is sold research-use-only, is not an approved drug, and has no clinical trials as a combination.
Mechanism
The three converge on energy metabolism by different routes. NAD+ is an essential redox coenzyme and substrate for sirtuins/PARPs/CD38. MOTS-c is a mitochondrial-derived peptide that activates AMPK and promotes metabolic homeostasis. 5-Amino-1MQ inhibits nicotinamide N-methyltransferase (NNMT), which is proposed to raise cellular NAD+ and SAM. The blend's rationale is converging support of the NAD+/mitochondrial axis, but the combined pharmacology has not been characterized, and the MOTS-c and 5-Amino-1MQ mechanisms are established only in cell and animal models.
Clinical evidence
There are no trials of this blend. Per component, the evidence is uneven: human RCTs exist for NAD+ precursors (nicotinamide riboside/NMN raise NAD+ but with limited proven clinical benefit, and IV NAD+ itself has only pilot data), while MOTS-c and 5-Amino-1MQ are preclinical-only with no human interventional trials. No controlled human evidence supports the combination for anti-aging, energy or metabolic outcomes; such claims should be treated as unproven.
Safety profile
The combined safety has not been studied. The most concrete acute issue is rapid IV NAD+, which commonly causes flushing, nausea and chest/abdominal tightness (mitigated by slowing the infusion); injection-site reactions apply to the subcutaneous components. Human safety of MOTS-c and 5-Amino-1MQ is essentially unstudied, and research-grade purity is unverified. None are FDA-approved, and the blend is not WADA-listed (though a high-volume IV NAD+ infusion is itself a banned method). Research-use only; nothing here is therapeutic or dosing guidance.
- During IV / per dose
IV NAD+ is infused slowly over hours (rapid infusion causes flushing). MOTS-c and 5-Amino-1MQ have no human time-course.
- Weeks
No trials of the blend exist; NAD+ precursors raise NAD+ over weeks without proven benefit, and the peptide/small-molecule components are preclinical. Any timeline is unverified.
Reported in published literature and user reports. Not a complete list, and not medical advice.
- Flushing, nausea, chest/abdominal tightness with rapid IV NAD+
- Injection-site reactions
- Human safety of MOTS-c and 5-Amino-1MQ is essentially unstudied
- Unstudied combined safety
If severe or unexpected symptoms occur, contact a qualified medical professional. PEPTIDES·INDEX does not provide medical advice.
- No human safety data exist for the combination; it is unstudied and research-use only.
- Rapid IV NAD+ commonly causes flushing, nausea and chest/abdominal tightness — infusions should be given slowly; this is the most concrete acute risk.
- Human safety of MOTS-c and 5-Amino-1MQ is essentially unstudied, and research-grade purity is unverified.
- No documented human drug interactionsNo interaction studies of the combination; uncharacterized in humans (research use only)
Compare
- vs NAD+
The single NAD+ component, the most-studied of the three.
- vs MOTS-c
The single mitochondrial-derived-peptide component (preclinical-only).
- vs 5-Amino-1MQ
The single NNMT-inhibitor component (a small molecule, preclinical-only).
FAQ
Is the NAD+/MOTS-c/5-Amino-1MQ blend studied in clinical trials?
No. There are no trials of this blend. Per component, human RCTs exist for NAD+ precursors (with limited proven clinical benefit), while MOTS-c and 5-Amino-1MQ are preclinical-only with no human interventional trials. Combined benefit is unproven.
What is in this blend?
Three agents that converge on cellular and mitochondrial energy metabolism — the redox coenzyme NAD+, the mitochondrial-derived peptide MOTS-c, and the NNMT inhibitor 5-Amino-1MQ (a small molecule, not a peptide).
Is it banned in sport?
The blend is not on the WADA Prohibited List, though a high-volume IV NAD+ infusion can itself fall under the prohibited-method rules on IV infusions.
Why combine NAD+, MOTS-c and 5-Amino-1MQ?
All three are proposed to support the NAD+/mitochondrial energy axis by different routes — NAD+ as a direct redox coenzyme, MOTS-c by activating AMPK, and 5-Amino-1MQ by inhibiting NNMT (which is proposed to raise cellular NAD+). The rationale is converging metabolic support, but the combined pharmacology has not been characterized and the MOTS-c and 5-Amino-1MQ mechanisms are established only in cell and animal models.
Why is rapid IV NAD+ a safety concern?
Infused too quickly, IV NAD+ commonly causes flushing, nausea and chest or abdominal tightness; this is the most concrete acute risk of the blend and is mitigated by slowing the infusion (NAD+ is typically given over hours). The subcutaneous components carry injection-site reactions, and the combined safety is otherwise unstudied. Research use only.
Is 5-Amino-1MQ a peptide?
No. 5-Amino-1MQ is a small-molecule NNMT inhibitor, not a peptide — so this is a mixed peptide/small-molecule blend rather than a pure peptide stack. Its activity is established only in animal models, with no human interventional trials, and research-grade purity is unverified.
Similar compounds
Starting references for the library summary. These are not dosing instructions or medical advice.
For research-use educational context only. Not medical advice and not a recommendation to use any compound. Consult a qualified healthcare professional before any health decision.