(4Z,6E)-5-Hydroxy-1,7-diphenylhepta-4,6-dien-3-one/(4Z,6E)-5-Hydroxy-1,7-diphenyl-4,6-heptadien-3-one
98%
- Product Code: 246754
CAS:
478313-96-1
| Molecular Weight: | 278.35 g./mol | Molecular Formula: | C₁₉H₁₈O₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 479.9±45.0 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, sealed, dry, light-proof |
Product Description:
Used primarily in research for its potential anti-inflammatory and antioxidant properties. Shows activity in cellular models related to oxidative stress and inflammation pathways. Investigated for possible applications in developing therapeutics for neurodegenerative diseases and cancer due to its ability to modulate signaling pathways such as NF-κB and MAPK. Also utilized as a reference compound in structure-activity relationship (SAR) studies of curcumin analogs, helping to design more stable and bioavailable derivatives. Its conjugated system and keto-enol tautomerism make it useful in photophysical studies and as a model compound in synthetic chemistry for exploring reaction mechanisms involving enones and dienones.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.005 | 10-20 days | $2,749.76 |
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(4Z,6E)-5-Hydroxy-1,7-diphenylhepta-4,6-dien-3-one/(4Z,6E)-5-Hydroxy-1,7-diphenyl-4,6-heptadien-3-one
Used primarily in research for its potential anti-inflammatory and antioxidant properties. Shows activity in cellular models related to oxidative stress and inflammation pathways. Investigated for possible applications in developing therapeutics for neurodegenerative diseases and cancer due to its ability to modulate signaling pathways such as NF-κB and MAPK. Also utilized as a reference compound in structure-activity relationship (SAR) studies of curcumin analogs, helping to design more stable and bioavailable derivatives. Its conjugated system and keto-enol tautomerism make it useful in photophysical studies and as a model compound in synthetic chemistry for exploring reaction mechanisms involving enones and dienones.
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