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#030Anti-Aging
>98%

VIP

Vasoactive Intestinal Peptide

Half-life: ~2 minutes (plasma, rapid degradation)

VIP peptideVasoactive intestinal polypeptidePHM-27 related

Research Profile

Research Depth
85
Potency
60
Half-Life Score
10
Selectivity
88
Stability
45

Relative research assessments — educational reference only.

Target Receptors

VPAC1VPAC2

Critical Research Warning

Research chemical — not for human consumption. Potent vasoactive and immunomodulatory peptide; cardiovascular effects possible. Not an approved drug.

PeptidePlaza Entry #030

"A 28-amino-acid neuropeptide with potent anti-inflammatory and immunomodulatory actions. Being studied for autoimmune diseases, type 2 diabetes, and antiviral applications."

Full Description

Vasoactive intestinal peptide (VIP) is a 28-amino-acid neuropeptide widely distributed in the nervous, endocrine, and immune systems. It was originally identified for its potent vasodilatory activity but is now recognized as a master immunomodulator: it inhibits pro-inflammatory cytokine production, promotes regulatory T-cell differentiation, and exerts anti-inflammatory effects in models of autoimmune and inflammatory disease. VIP signaling via VPAC1/VPAC2 receptors is being studied in type 2 diabetes, Sjögren’s syndrome, osteoarthritis, inflammatory bowel disease, and as a potential antiviral target (including effects on SARS-CoV-2). Synthetic VIP and stable analogs are in development.

Mechanism of Action

Binds VPAC1 and VPAC2 G-protein-coupled receptors, activating adenylate cyclase and cAMP/PKA signaling, which modulates cytokine gene transcription (NF-κB inhibition), promotes regulatory T cells, and suppresses Th1/Th17 inflammatory responses.

Reported Benefits

  • Potent anti-inflammatory and immunomodulatory actions
  • Promotes regulatory T-cell responses in models
  • Studied for type 2 diabetes via VPAC2 agonism
  • Potential antiviral and tissue-protective roles

Potential Side Effects

  • Rapid degradation limits dosing practicality
  • Vasodilation / flushing at higher doses
  • GI motility effects (diarrhea)
  • Limited human safety data

Frequently Asked Questions

What is VIP known for?
VIP is a neuropeptide with strong anti-inflammatory and immunomodulatory properties. It was first discovered as a vasodilator but is now studied for autoimmune disease, diabetes, and neuroprotection.
Why is VIP hard to use as a drug?
VIP is rapidly degraded in plasma (half-life of ~2 minutes) and acts on multiple receptor subtypes, so most drug development uses stable analogs or modified formulations. This is a major translational challenge.
What conditions is VIP being studied for?
Models and trials target type 2 diabetes (VPAC2), Sjögren’s syndrome, osteoarthritis, inflammatory bowel disease, and antiviral applications including SARS-CoV-2.

For Research Reference Only

Not medical advice. Peptides may be regulated or restricted in your jurisdiction.

References

  1. 1.Therapeutic potential of vasoactive intestinal peptide and its receptor VPAC2 in type 2 diabetes.. PubMed (2022). Hou X, et al.. pubmed.ncbi.nlm.nih.gov/36204104/
  2. 2.Vasoactive intestinal peptide: a potential target for antiviral therapy.. PubMed (2022). He Y, et al.. pubmed.ncbi.nlm.nih.gov/35770640/

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