VIP (Vasoactive Intestinal Peptide) Research Standard
Vasoactive Intestinal Peptide (VIP) is a 28-amino-acid neuropeptide that plays a pivotal role in signaling across various biological systems. As a member of the secretin/glucagon superfamily, synthetic porcine VIP is extensively utilized in laboratory research to investigate G-protein-coupled receptor (GPCR) systems, specifically the VPAC1 and VPAC2 receptors. By acting as a high-affinity ligand for these receptors, VIP serves as a critical probe for examining intracellular signaling cascades, particularly the stimulation of cyclic AMP (cAMP) pathways, in controlled in vitro and cellular models.
Technical Specifications
| Property | Specification |
| Product Name | VIP (Vasoactive Intestinal Peptide) |
| UNII / Synonym | 6J2WVD66KR |
| CAS Number | 37221-79-7 |
| Chemical Formula | C147H237N43O43S |
| Molecular Weight | 3326.8 g/mol |
| Peptide Length | 28 amino acids |
| Chemical Class | Neuropeptide |
| Physical Appearance | White to off-white lyophilized powder |
| Assay Purity | >= 98% (HPLC verified) |
Mechanism of Action & Research Context
VIP is investigated for its specific engagement with G-protein-coupled receptors, functioning as a primary tool for exploring receptor-mediated signaling kinetics.
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Receptor Interaction: The peptide is studied for its high-affinity binding to VPAC1 and VPAC2 receptors, which are crucial for cellular homeostasis and neural signaling.
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cAMP Pathway Signaling: VIP is used to characterize the activation of adenylyl cyclase, which leads to the production of cyclic AMP (cAMP). This makes it an essential tool for quantifying GPCR-mediated downstream effects in isolated tissue or cell-line models.
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Structural Specificity: Research centers on the 28-amino-acid sequence, ensuring that structural modifications in experimental analogs can be benchmarked against the full-length peptide to determine selectivity and binding efficacy.
Research Applications
VIP is a specialized reagent essential for modern endocrinology and neuro-pharmacological research.
Primary fields of in vitro laboratory investigation include:
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Receptor Binding Assays: Quantifying the affinity and selectivity of ligand interactions with VPAC1 and VPAC2 receptors.
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Binding Kinetics: Determining the association ($k_{on}$) and dissociation ($k_{off}$) rates in receptor-ligand complex formation.
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Antagonist & Analog Studies: Benchmarking modified peptide analogs or receptor antagonists against native VIP to identify pharmacophore requirements.
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Cell Culture Models: Evaluating receptor expression levels and signaling responsiveness in varied cell lines under standardized conditions.
Storage & Handling Guidelines
To maintain the chemical stability and experimental reliability of the peptide:
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Lyophilized Storage: Store in a cool, dry place. The lyophilized powder can be maintained at room temperature for short-term handling, provided it is protected from direct light.
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Long-term Storage: Keep sealed containers at -20°C for extended stability.
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Reconstituted Stability: If reconstituted in a buffer, store the resulting solution refrigerated (2°C – 8°C). Avoid repeated freeze-thaw cycles to prevent degradation of the peptide sequence.
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Aseptic Technique: Always use sterile, dry equipment to draw samples. Ensure the container remains tightly sealed between uses to prevent moisture ingress and cross-contamination.
Research Use Disclaimer
Research Use Only Disclaimer: This product is developed and distributed strictly as a Research Use Only (RUO) laboratory reference chemical intended exclusively for non-clinical analytical and scientific investigation. It is not an FDA-approved drug, medical treatment, dietary supplement, or food ingredient, and is strictly prohibited for human or animal consumption. Kimera Chems supplies this high-purity research material solely to qualified institutions and professional investigators for authorized laboratory research.
| CAS Number | 37221-79-7 |
| Other Names | VASOACTIVE INTESTINAL PEPTIDE, UNII-6J2WVD66KR, 6J2WVD66KR, CCRIS 7231, Vasoactive intestinal peptide, synthetic porcine |
| IUPAC Name | (2S)-4-amino-2-[[(2S)-2-[[(2S,3S)-2-[[(2S)-2-[[(2S)-4-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-6-amino-2-[[(2S)-6-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-5-amino-2-[[(2S)-6-amino-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S,3R)-2-[[(2S)-2-[[(2S)-4-amino-2-[[(2S)-2-[[(2S,3R)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-amino-3-(1H-imidazol-4-yl)propanoyl]amino]-3-hydroxypropanoyl]amino]-3-carboxypropanoyl]amino]propanoyl]amino]-3-methylbutanoyl]amino]-3-phenylpropanoyl]amino]-3-hydroxybutanoyl]amino]-3-carboxypropanoyl]amino]-4-oxobutanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]-3-hydroxybutanoyl]amino]-5-carbamimidamidopentanoyl]amino]-4-methylpentanoyl]amino]-5-carbamimidamidopentanoyl]amino]hexanoyl]amino]-5-oxopentanoyl]amino]-4-methylsulfanylbutanoyl]amino]propanoyl]amino]-3-methylbutanoyl]amino]hexanoyl]amino]hexanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]amino]-4-methylpentanoyl]amino]-4-oxobutanoyl]amino]-3-hydroxypropanoyl]amino]-3-methylpentanoyl]amino]-4-methylpentanoyl]amino]-4-oxobutanoic acid |
| Molecular Formula | C₁₄₇H₂₃₇N₄₃O₄₃S |
| Molecular Weight | 3325.80 |



