structure of StilbosteMin N

StilbosteMin N

CAS No.: 1000676-45-8
M. Wt: 258.31
M. Fa: C16H18O3
InChI Key: -

Names and Identifiers of StilbosteMin N

CAS Number

1000676-45-8

IUPAC Name

3-methoxy-5-[2-(2-methoxyphenyl)ethyl]phenol

Canonical SMILES

COC1=CC=CC=C1CCC2=CC(=CC(=C2)OC)O

Physical and chemical properties of StilbosteMin N

Boiling Point

742.2±60.0 °C at 760 mmHg

Density

1.5±0.1 g/cm3

Exact Mass

680.074158

Flash Point

402.7±32.9 °C

Index of Refraction

1.634

LogP

12.81

Molecular Formula

C16H18O3

Molecular Weight

258.31

PSA

100.48000

Vapour Pressure

0.0±2.5 mmHg at 25°C

Applications of StilbosteMin N

Stilbostemin N has several potential applications:

  • Pharmaceutical Development: Its antimicrobial and anti-inflammatory properties make it a candidate for drug development targeting infections and inflammatory conditions.
  • Agricultural Uses: Given its natural origin and bioactivity, stilbostemin N may be explored as a natural pesticide or fungicide.
  • Food Industry: The antioxidant properties could be utilized in food preservation or enhancement of nutritional profiles.

These applications underscore the versatility of stilbostemin N in various industries.

Interaction Studies of StilbosteMin N

Research on the interactions of stilbostemin N with biological molecules is ongoing. Key areas of study include:

  • Protein Binding Studies: Understanding how stilbostemin N interacts with proteins can reveal mechanisms of action for its biological effects.
  • DNA Interaction: Investigating how stilbostemin N binds to DNA could elucidate its potential anticancer properties.
  • Metabolic Pathways: Studies on how this compound is metabolized in vivo can provide insights into its efficacy and safety profiles.

These interaction studies are vital for advancing the understanding of stilbostemin N's biological significance.

Biological Activity of StilbosteMin N

Stilbostemin N exhibits a range of biological activities, primarily attributed to its structural features. Some key activities include:

  • Antimicrobial Properties: Like other stilbenoids, stilbostemin N has shown efficacy against various bacterial strains, making it a candidate for developing antimicrobial agents.
  • Antioxidant Effects: The compound may act as an antioxidant, scavenging free radicals and reducing oxidative stress in biological systems.
  • Anti-inflammatory Activity: Stilbostemin N could modulate inflammatory pathways, contributing to its potential therapeutic applications in inflammatory diseases.

These biological properties highlight the significance of stilbostemin N in medicinal chemistry and pharmacology.