PIPERINE

Piperine is a bioactive alkaloid that enhances nutrient absorption by modulating drugmetabolizing enzymes and transporters. It also exhibits antioxidant and antiinflammatory activity. Benefits include improved bioavailability of certain compounds. Side effects are generally mild but may involve gastrointestinal irritation, burning sensation, or interactions that raise blood levels of coadministered medications. Only GMP materials will be supplied, logistics all according to GDP.

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Product Description


Scientific Overview

PIPERINE is a researchgrade biochemical compound used for advanced analytical, mechanistic and structural studies. It is often applied in laboratory environments requiring precise molecular behaviour, controlled pathway modulation and highfidelity reproducibility. The compound interacts with multiple biochemical systems depending on formulation, cell type and experimental conditions.

Mechanism of Action

Although the exact mechanism may vary by experimental model, PIPERINE typically exhibits activity involving:

  • Enzymatic pathway modulation through reversible or irreversible interaction with catalytic sites
  • Potential receptorlevel signaling effects influencing intracellular second messengers
  • Alterations in redox balance and oxidativestress handling systems
  • Mitochondrial functional modulation, including effects on ATP turnover and respiratorychain efficiency
  • Influence on transcriptional behaviour, geneexpression clusters and regulatory protein networks
  • Possible interaction with cytoskeletal structures affecting cellular stability and mechanical signaling

These combined effects make the compound suitable for multiaxis biochemical research.

Benefits and Applications

PIPERINE is commonly used for:

  • Pathway validation and mechanistic investigation
  • Bindingaffinity studies and structural modelling
  • Metabolicflux analysis and mitochondrialfunction profiling
  • Redox and oxidativestress research environments
  • Cytoskeletal and membranedynamic studies
  • Signaltransduction mapping across diverse biological systems

Risks and Safety Considerations

Potential risks associated with laboratory exposure include:

  • Oxidative imbalance or ROS accumulation
  • Mitochondrial stress or functional suppression at high concentrations
  • Unintended receptor or enzyme crossinteraction
  • Cytoskeletal destabilization or membrane disturbance
  • Dosedependent cytotoxicity under prolonged exposure

Handle only with appropriate laboratory biosafety protocols.

Only GMP materials will be supplied, logistics all according to GDP.

Datasheet


Molecular Formula

C17H19NO3

Molecular Weight

285.34 g/mol

CAS Number

94-62-2

Storage Condition

Store in a cool, dry place. Keep container tightly closed. Protect from moisture and light.

Solubility

0.04 mg/mL at 18 °C

Purity

Purity information is available upon request (COA).

Synonym

piperine; 94-62-2; 1-Piperoylpiperidine; Piperin; Bioperine

IUPAC/Chemical Name

(2E,4E)-5-(1,3-benzodioxol-5-yl)-1-piperidin-1-ylpenta-2,4-dien-1-one

InChl Key

MXXWOMGUGJBKIW-YPCIICBESA-N

InChl Code

InChI=1S/C17H19NO3/c19-17(18-10-4-1-5-11-18)7-3-2-6-14-8-9-15-16(12-14)21-13-20-15/h2-3,6-9,12H,1,4-5,10-11,13H2/b6-2+,7-3+

References

https://pubchem.ncbi.nlm.nih.gov/compound/638024;

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