(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%

Reagent Code: #246754
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CAS Number 478313-96-1

science Other reagents with same CAS 478313-96-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 278.35 g/mol
Formula C₁₉H₁₈O₂
thermostat Physical Properties
Boiling Point 479.9±45.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description 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.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿64,600.00

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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
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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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