Stilbene-3,4'-diol
CAS No.:
63877-76-9
M. Wt:
212.24
M. Fa:
C14H12O2
InChI Key:
UFGKEFGYNRJIGO-SNAWJCMRSA-N
Names and Identifiers of Stilbene-3,4'-diol
CAS Number |
63877-76-9 |
|---|---|
EC Number |
850-856-1 |
IUPAC Name |
3-[(E)-2-(4-hydroxyphenyl)ethenyl]phenol |
InChI |
InChI=1S/C14H12O2/c15-13-8-6-11(7-9-13)4-5-12-2-1-3-14(16)10-12/h1-10,15-16H/b5-4+ |
InChIKey |
UFGKEFGYNRJIGO-SNAWJCMRSA-N |
Canonical SMILES |
C1=CC(=CC(=C1)O)C=CC2=CC=C(C=C2)O |
Isomeric SMILES |
C1=CC(=CC(=C1)O)/C=C/C2=CC=C(C=C2)O |
UNII |
4DC9L42B37 |
Physical and chemical properties of Stilbene-3,4'-diol
Molecular Formula |
C14H12O2 |
|---|---|
Molecular Weight |
212.24 |
Safety Information of Stilbene-3,4'-diol
Applications of Stilbene-3,4'-diol
Stilbene-3,4'-diol finds applications across several domains:
- Pharmaceuticals: Due to its biological activity, it is explored as a potential therapeutic agent against cancer and oxidative stress-related diseases.
- Materials Science: Its photochemical properties make it useful in developing light-emitting materials and sensors.
- Agriculture: Compounds similar to stilbene-3,4'-diol are investigated for their potential as natural pesticides or growth regulators.
Interaction Studies of Stilbene-3,4'-diol
Studies have focused on the interactions of stilbene-3,4'-diol with various biological targets:
- Enzyme Inhibition: Research indicates that it may inhibit specific enzymes involved in cancer progression and inflammation pathways.
- Receptor Binding: Interaction studies suggest that stilbene derivatives can bind to estrogen receptors, potentially influencing hormonal pathways.
These interactions underline its potential therapeutic applications.
Biological Activity of Stilbene-3,4'-diol
Stilbene-3,4'-diol exhibits various biological activities:
- Antioxidant Properties: It has been shown to scavenge free radicals, contributing to its potential use in preventing oxidative stress-related diseases.
- Anticancer Activity: Research indicates that stilbene derivatives can inhibit cancer cell proliferation and induce apoptosis in certain cancer types.
- Anti-inflammatory Effects: The compound has demonstrated the ability to reduce inflammation markers in vitro and in vivo models.
These properties make it a subject of interest for drug development.
