Informational only. Not medical advice.INFORMATIONAL PLATFORM ONLY — NOT MEDICAL ADVICE, DIAGNOSIS, OR TREATMENT
Informational only. Not medical advice.INFORMATIONAL PLATFORM ONLY — NOT MEDICAL ADVICE, DIAGNOSIS, OR TREATMENT
Head-to-head comparison of DSIP and NAD+ — mechanism, side effects, legal status, and pricing.
DSIP (Delta Sleep-Inducing Peptide) is a nonapeptide (Trp-Ala-Gly-Gly-Asp-Ala-Ser-Gly-Glu) isolated in 1977 by Schoenenberger and Monnier from cerebral venous blood of rabbits during electrically induced sleep. It has been studied as a putative sleep and stress modulator, but the evidence base is weak, largely pre-2000, and DSIP is not FDA-approved.
NAD+ (nicotinamide adenine dinucleotide) is a coenzyme present in all living cells, not a peptide. It is classified here alongside peptides for user convenience in the anti-aging / metabolic category. NAD+ plays a central role in cellular energy metabolism and redox reactions and is studied for its involvement in mitochondrial function, DNA-damage signaling via sirtuins and PARPs, and age-associated metabolic decline. IV NAD+ is not FDA-approved for any clinical indication; it is administered off-label through compounding pharmacies and functional-medicine clinics with limited rigorous outcome data.
DSIP
NAD+
Category
Legal Status
Mechanism
Half-life
Side Effects
COA-verified vendors · trust score ≥70 required · single-vial price — bulk/bundle deals may be lower
DSIP
NAD+
COA corpus from Disclosed Labs — independently tested batches only.
DSIP
69
COAs
99.4%
Avg purity
14
Labs
NAD+
146
COAs
99.4%
Avg purity
15
Labs
DSIP is among peptides under FDA review for the Category 1 (503A) list; if added, it would require a prescription to be compounded by registered 503A/503B pharmacies — not yet authorized. NAD+ remains research-only. In April 2026 the FDA removed 12 peptides from Category 2, which does not place them on the Category 1 list or authorize compounding. The FDA's Pharmacy Compounding Advisory Committee is advisory and meets July 23–24, 2026 to review nominations and make recommendations to the FDA.
Schoenenberger & Monnier first isolated and characterized DSIP in 1977 (PNAS 74(3):1282-6, PMID 265572). Graf & Kastin's 1984 review (Neurosci Biobehav Rev, PMID 6145137) summarized the first decade of work, noting reported effects on sleep, pain, and stress but also substantial inconsistency across labs and species. Schneider-Helmert (Eur Neurol 1986, PMID 3792404) reported sleep normalization in 18 middle-aged and elderly chronic insomniacs given DSIP over one week — small, open, and never replicated at scale. Schneider-Helmert et al. (Dtsch Med Wochenschr 1987, PMID 3582201) explored phase-shifted insomnia. Kovalzon & Strekalova (J Neurochem 2006, PMID 16539679) summarized the field as a 'still unresolved riddle,' noting that no DSIP receptor or gene has been identified. No Phase 3 trials, no FDA approval, no modern controlled replication.
Key references
The strongest human evidence for raising circulating NAD+ comes from oral-precursor trials. A randomized, double-blind, placebo-controlled study of nicotinamide riboside combined with pterostilbene (NRPT) showed sustained dose-dependent increases in whole-blood NAD+ over 8 weeks in healthy adults (Dellinger et al., npj Aging and Mechanisms of Disease, 2017). A Yoshino/Baur/Imai review summarizes the biology and emerging therapeutic potential of NR and NMN, including preclinical healthspan data in aged mice (Cell Metabolism, 2018). Direct IV NAD+ has only small pilot pharmacokinetic data: Grant et al. infused 750 mg over 6 hours in 8 healthy men and documented altered plasma and urine NAD+ metabolome without clinical-outcome endpoints (Frontiers in Aging Neuroscience, 2019). No adequately powered RCTs support IV or SubQ NAD+ for anti-aging, cognition, addiction, or Parkinson's disease; clinic marketing claims outrun the published outcome evidence.
DSIP (Cognitive) and NAD+ (Metabolic) are in different categories and target different biological pathways. This is a common pattern in multi-compound research protocols. Researchers should monitor the biomarkers from both profiles and watch for interactions listed in each compound’s contraindications. Consult a licensed healthcare provider before combining any research compounds.
This platform provides informational tools only, not medical advice. This comparison is for educational purposes only. Consult a licensed provider.
Contraindications
Lab Testing
Key references
Disclosed Labs