
VIP 5mg
VIP — Overview
Vasoactive Intestinal Peptide (VIP) is a 28‑amino‑acid neuropeptide belonging to the secretin/glucagon superfamily. It is widely distributed throughout the central and peripheral nervous systems, gastrointestinal tract, and immune tissues, and is known for its potent vasodilatory, anti‑inflammatory, immunomodulatory, and neuroprotective properties.
Biological Role & Mechanism
VIP functions as both a neurotransmitter and neuromodulator, acting on three primary receptors:
- VPAC1
- VPAC2
- PAC1
These receptors activate cAMP‑mediated signaling pathways, influencing smooth muscle relaxation, epithelial secretion, immune cell behavior, and blood flow regulation.
VIP is released from nerve terminals and acts locally as a neurohormone and paracrine mediator, coordinating responses across multiple organ systems.
Key Research Characteristics
| Attribute | Details |
| Peptide Type | Endogenous neuropeptide |
| Length | 28 amino acids |
| Receptors | VPAC1, VPAC2, PAC1 |
| Primary Actions | Vasodilation, anti‑inflammatory signaling, immunomodulation, smooth muscle relaxation |
| Half‑Life | ~1–2 minutes in plasma; ~20 minutes in tissue |
| Molecular Weight | ~3326.8 g/mol |
Research Applications
VIP is commonly studied in models involving:
- Inflammation and immune modulation
- Respiratory pathways (e.g., asthma, COPD)
- Neuroprotection and neurodegenerative research
- Gastrointestinal motility and secretion
- Circadian rhythm regulation
Its extremely short plasma half‑life makes it a valuable model for studying rapid‑acting neuropeptides and peptide stability.
Form & Handling (Research Context)
- Form: Lyophilized powder
- Storage: 2–8°C refrigerated; protect from light
- Stability: Very short once reconstituted (minutes)
For laboratory research only. Not for human consumption.
Certificate of Analysis (COA) images are provided for this product.




