No. 043 · Longevity & Immune · Cellular Health
NAD+
Also known as: Nicotinamide adenine dinucleotideNADNadideCoenzyme I
- Not FDA approved
- WADA — not listed
- Not a peptide
2D structure from PubChem CID 5892 (Nadide), matched by molecular formula. Hydrogens on carbon are implied.
NAD+ is not a peptide, so it has no amino-acid sequence. This ring motif is decorative.
Quick answers
- What is NAD+?
- Nicotinamide adenine dinucleotide, a coenzyme central to cellular energy production and sirtuin-mediated DNA repair. NAD+ is a dinucleotide coenzyme (nicotinamide + adenine nucleotides), not a peptide. It is listed here because it is sold and used alongside peptides.
- How strong is the evidence for NAD+?
- Tier A (controlled human trials) on the peptidemeta evidence scale. A randomized placebo-controlled trial of intravenous NAD+ in 180 patients with ischemic heart failure (2025), plus small pilot and pharmacokinetic studies. Most other trials test precursors (NR, NMN), which are different compounds.
- Is NAD+ FDA-approved?
- No. NAD+ is not approved by the FDA for any use. Outside the US: China — NAD+ for injection (“Coenzyme I for injection”), NMPA-registered.
- Is NAD+ banned in sport?
- No. NAD+ is not on the World Anti-Doping Agency Prohibited List.
- How does NAD+ work?
- NAD+ is an essential coenzyme that accepts electrons in glycolysis, the TCA cycle, and beta-oxidation, feeding them into the mitochondrial electron transport chain for ATP production. It also serves as a substrate for sirtuins (SIRT1-7), which deacetylate histones and proteins to regulate DNA repair, mitochondrial biogenesis, and inflammatory responses.
- What is known about the safety of NAD+?
- Endogenous coenzyme with well-characterized biology. IV NAD+ infusions can cause chest tightness, nausea, and cramping during rapid administration (rate-dependent).
Last reviewed · editorial policy · markdown
Evidence
- D In vitro
- C Animal
- B Human pilot
- A RCT
- S Approved
TIER A — At least one published randomized controlled trial in humans.
A randomized placebo-controlled trial of intravenous NAD+ in 180 patients with ischemic heart failure (2025), plus small pilot and pharmacokinetic studies. Most other trials test precursors (NR, NMN), which are different compounds.
Tiers rate the strength of published evidence — not effectiveness, safety, or a recommendation.
At a glance
- Molecular weight
- 663.4 Da
- Formula
- C21H27N7O14P2
- Routes studied
- Intravenous, Oral, Subcutaneous Routes used in published research
- FDA
- Not approved
- Other approvals
-
- China — NAD+ for injection (“Coenzyme I for injection”), NMPA-registered
- WADA
- Not on the Prohibited List
Overview
Nicotinamide adenine dinucleotide, a coenzyme central to cellular energy production and sirtuin-mediated DNA repair. Declining NAD+ levels are a hallmark of biological aging.
Research status Extensive human and animal research on NAD+ biology; a randomized placebo-controlled trial of IV NAD+ in ischemic heart failure (2025); NR/NMN precursors tested in multiple clinical trials
Mechanism
NAD+ is an essential coenzyme that accepts electrons in glycolysis, the TCA cycle, and beta-oxidation, feeding them into the mitochondrial electron transport chain for ATP production. It also serves as a substrate for sirtuins (SIRT1-7), which deacetylate histones and proteins to regulate DNA repair, mitochondrial biogenesis, and inflammatory responses. NAD+ decline with age impairs these pathways.
Effects reported in research
Reported outcomes, not promises. Some come from controlled human trials; others may be from smaller or preclinical studies — check the studies below.
- Restored cellular energy metabolism
- Activated sirtuin-mediated DNA repair
- Improved mitochondrial function
- Enhanced mental clarity and reduced fatigue
Safety & unknowns
Endogenous coenzyme with well-characterized biology. IV NAD+ infusions can cause chest tightness, nausea, and cramping during rapid administration (rate-dependent). NR and NMN oral precursors are generally well-tolerated in clinical trials. Flushing possible with high-dose niacin (a different NAD+ precursor). Widely available as supplements.
Unknowns. Trial safety data apply to the populations, formulations and conditions studied.
Informational only — not medical advice. peptidemeta publishes no dosing, protocols, or sourcing. Talk to a qualified clinician about any treatment decision.
Studies [3]
- Clinical trial 2026
Effect of Nicotinamide Adenine Dinucleotide on Heart Failure Caused by Ischemic Cardiomyopathy: A Randomized, Placebo-Controlled Trial
Single-center RCT in 180 patients with ischemic heart failure: 7 days of IV NAD+ added to standard therapy produced a greater improvement in ejection fraction at 1 month than placebo; differences in clinical events were not statistically significant.
- Review 2021
NAD+ metabolism and its roles in cellular processes during ageing
Review of NAD+ metabolism in ageing, covering its synthesis, consumption by enzymes such as sirtuins and PARPs, and strategies to restore NAD+ levels.
- Clinical trial 2018
Chronic nicotinamide riboside supplementation is well-tolerated and elevates NAD+ in healthy middle-aged and older adults
Randomized, double-blind, placebo-controlled crossover trial (2 × 6 weeks) in which the NAD+ precursor nicotinamide riboside was well tolerated and raised NAD+ metabolism; it tested the precursor, not NAD+ itself.
Status sources
Sources behind the tier, regulatory status, sequence and dates on this page.
- Yu et al., Am J Cardiovasc Drugs 2026 — intravenous NAD+ in ischemic cardiomyopathy heart failure, RCT pubmed.ncbi.nlm.nih.gov
- Grant et al. 2019 — pilot pharmacokinetic study of a 6-hour IV NAD+ infusion pubmed.ncbi.nlm.nih.gov
- PubChem CID 5892 (NAD) pubchem.ncbi.nlm.nih.gov
- NMPA approval-document notice listing Coenzyme I for injection (2026) nmpa.gov.cn
- WADA 2026 Prohibited List (not named; IV infusions over 100 mL per 12 h are banned under M2.2) wada-ama.org
Cite this entry
peptidemeta. (2026). NAD+. In peptidemeta: The peptide library, ranked by evidence. Retrieved November 8, 2026, from https://peptidemeta.com/p/nad-plus/
@misc{peptidemeta-nad-plus,
title = {NAD+},
author = {{peptidemeta}},
year = {2026},
howpublished = {\url{https://peptidemeta.com/p/nad-plus/}},
note = {Accessed 2026-11-08}
} Accessed date reflects when you opened this page. Cite primary studies for scientific claims.