VIP
Vasoactive Intestinal Peptide
VIP is a 28-amino-acid neuropeptide isolated by Said and Mutt in 1970. It acts at VPAC1/VPAC2 and is a potent vasodilator with a minutes-class IV half-life. Intranasal research use shows up in Shoemaker CIRS open-label work (n=20, 2013), which is not a Phase 3 trial. Aviptadil (synthetic VIP) had separate pulmonary development. This page is identity and honesty, not a mold-illness cure.
Use-case scores
0–10 against the evidence we have, not a gym ranking. Hidden domains do not apply here.
- Immune4/10
VPAC immunoregulation is real physiology. The CIRS open-label n=20 sits at small-human / community after honesty haircuts. Not a 6.5 without a controlled trial.
Compound card
- Sequence
- 28-aa VIP (HSDAVFTDNYTRLRKQMAVKKYLNSILN-NH2)
- Class
- Endogenous VPAC1/VPAC2 neuropeptide
- Formula
- C147H237N43O43S
- Status
- Not FDA-approved · research use
How it works
VIP is a 28-residue neuropeptide isolated by Said and Mutt from porcine intestine (Science 1970, PMID 5450698). It is a potent vasodilator and a VPAC1/VPAC2 agonist with a minutes-class IV half-life. That physiology is not in dispute.
What this catalog page is usually asked to do is CIRS / mold / “Shoemaker protocol” nasal VIP. The 2013 open-label series (Health, DOI 10.4236/health.2013.53053, n=20) is that literature. It is not a Phase 3 RCT, not PubMed 28694751 (that PMID was a bad citation on this leaf), and not a reason to skip the rest of a clinician-run workup. Aviptadil is synthetic VIP in pulmonary development; it is not a research-chem nasal spray.
This site will not treat CIRS, MCAS, PAH, or Long COVID from a peptide page.
Source: PMID: 15271596
Not a reconstitution peptide on this site
VIP is typically a compounded nasal spray in the use-case people search. This database has no vial size. Do not force spray math into the SubQ calculator.
Goal context
CIRS as a clinic protocol, not a SKU
Shoemaker’s sequence puts VIP last, after exposure control and other steps, with lipase monitoring in that playbook. A peptide page cannot run that protocol.
Vasodilation is the side effect and the mechanism
Flushing and blood-pressure drop are expected pharmacology. First-dose hypotension is why clinic protocols watch the first spray.
Background & History
VIP is a 28-aa neuropeptide isolated by Said and Mutt in 1970. Minutes-class IV half-life, potent vasodilator, VPAC1/VPAC2. Nasal CIRS use is an open-label 2013 series (n=20), not a Phase 3. PMID 28694751 does not identify that paper. Aviptadil is a different development path. Not a reconstitution peptide in this database.
Research Use Cases
- ✓VIP identity and VPAC physiology
- ✓Understanding why CIRS clinics use a spray (not a SubQ calculator)
- ✓Not a mold-illness, MCAS, PAH, or Long-COVID cure page
Dosing
| Phase | Dose | Frequency | Notes |
|---|---|---|---|
| Shoemaker-style nasal (clinic playbook, unlabeled as a drug) | 50 mcg | Up to 4× daily intranasal in that protocol | Copied from the 2013 open-label paper’s starting cadence. Not an FDA label. First dose in-office in that playbook. |
Administration
Timeline
Who it is for
Need VIP identity
ModerateThis is the 28-mer. Physiology is real.
Need a mold-illness cure
LowWrong page.
Safety & Considerations
Potent vasodilator. Hypotension, flushing, diarrhea are class effects. Active diarrhea is a reason to stop in clinic playbooks that also watch lipase. Research/compounded nasal VIP is not aviptadil. Not for unsupervised first-dose heroics.
Regulatory & Legal Status
Not currently on the WADA 2026 Prohibited List. Policies may change - verify before competition.
Research Chemical
US Compounding: Not eligible / not available
⚠️ This information is for educational purposes only and may not reflect the most current regulatory updates. Always verify with official FDA, WADA, and jurisdiction-specific sources before use.
Limits of current evidence
- Shoemaker 2013 is open-label n=20 in a non-NEJM journal. Durable-efficacy language in that paper is the authors’. It is not a regulator’s.
- PMID 28694751 does not identify that paper. Cite the 2013 Health DOI instead of a hallucinated PMID.
- Aviptadil / PAH / COVID development is a different product path.
- IV half-life of minutes is why nasal or infusion exists. It is not a SubQ recovery depot.
- This leaf has no vial fill in the calculator database. Do not invent one.
Verdict
VIP is a real neuropeptide with a 1970 isolation paper. Nasal CIRS use is an open-label clinic protocol, not a Phase 3. Do not put a spray into the reconstitution calculator, and do not treat mold illness from this leaf.
Interactions & Contraindications
Vasodilation / hypotension, especially with antihypertensives. Diarrhea and lipase watching appear in CIRS playbooks. First-dose blood pressure is the practical hazard.
Synergies & Common Stacks
Both show up in inflammatory folklore. Different receptors. Not a combination trial.
Frequently Asked Questions
Is VIP a recovery peptide?▼
Does nasal VIP cure CIRS?▼
What PMID is the Shoemaker VIP paper?▼
Can I reconstitute a VIP vial in the calculator?▼
Is this aviptadil?▼
Why is the half-life 2 minutes?▼
First-dose caution?▼
FDA-approved?▼
References
- Said SI, Mutt V “Polypeptide with broad biological activity: isolation from small intestine.” Science (1970). PMID: 5450698
- Shoemaker RC, House D, Ryan JC “Vasoactive intestinal polypeptide (VIP) corrects chronic inflammatory response syndrome (CIRS) acquired following exposure to water-damaged buildings.” Health (2013). DOI: 10.4236/health.2013.53053
- Petkov V, et al. “Vasoactive intestinal peptide as a new drug for treatment of primary pulmonary hypertension.” J Clin Invest (2003). PMID: 12618522
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Affiliate link · Full review