Smooth Muscle Models
Relaxation endpoints are characterised in vascular and gastrointestinal tissue preparations.

Vasoactive Intestinal Peptide Studies
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Researchers also added
Research use only.
The Eon standard
Your results are only as good as your compound.
Every lot of VIP is tested by an independent ISO/IEC 17025-accredited lab in the USA. 99%+ purity isn't a target here. It's the requirement.
Don't take our word for it: test any vial at an accredited lab of your choice. If HPLC purity comes back under 99%, we refund your order and pay for the test.
VIP is a 28-amino acid neuropeptide of the secretin family, studied at the VPAC1 and VPAC2 receptors. Published research covers smooth-muscle relaxation, immunomodulation and neuroprotection endpoints, with cyclic AMP signalling as the principal characterised second messenger. For laboratory research use only.
28-residue neuropeptide studied at VPAC1 and VPAC2 receptors
The numbers that define VIP and how it is being studied. For laboratory research use only.
Secretin peptide family
Lyophilized powder
Class B GPCRs
The pathways VIP acts on - and what each one does. The animation traces its signal outward from the compound to every target it engages.
VIP binds the class B G-protein-coupled receptors VPAC1 and VPAC2. Adenylate cyclase activation and cyclic AMP accumulation are the principal characterised readouts.
Smooth-muscle relaxation endpoints are long characterised for VIP across vascular and gastrointestinal tissue preparations.
VIP is studied as an endogenous anti-inflammatory mediator, with cytokine-profile shifts measured in immune cell culture.
The main areas VIP is being studied for - and the study-reported figures behind them.
Relaxation endpoints are characterised in vascular and gastrointestinal tissue preparations.
Cytokine-profile endpoints are measured in immune cell culture.
VIP appears in neuroprotection literature alongside its receptor-signalling characterisation.
Used as a characterised VPAC-receptor agonist reference in assay development.
An interactive 3D model rendered from the compound record - rotate and explore its structure.
Molecular model
| Chemical Name | VIP (vasoactive intestinal peptide) |
| Length | 28 amino acids |
| Family | Secretin peptide family |
| Content | 10 mg per vial |
| Receptor Targets | VPAC1, VPAC2 (class B GPCRs) |
| Second Messenger | Cyclic AMP |
| Form | Lyophilized powder |
| Purity | ≥99% by HPLC |
| Solubility | Water-soluble |
| Storage | -20°C, protected from light |
| Classification | Research use only |
VPAC1 and VPAC2, both class B G-protein-coupled receptors. Adenylate cyclase activation and cyclic AMP accumulation are the principal characterised readouts.
The molecular weight will be published here from the lot's Certificate of Analysis rather than quoted from a secondary source.
Yes. Both belong to the secretin peptide family and share the VPAC receptors, which is why they are frequently studied together.
Each lot is analysed by reverse-phase HPLC and released at ≥99%, with a Certificate of Analysis.
Store lyophilized at -20°C for long-term stability, protected from light and moisture, and avoid repeated freeze-thaw cycles.
Not for human or veterinary use. For in-vitro laboratory research only. These statements have not been evaluated by the FDA; this product is not intended to diagnose, treat, cure, or prevent any disease. Sold exclusively to qualified researchers and institutions.