Cepharadione B

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Reagent Code: #163846
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CAS Number 55610-02-1

science Other reagents with same CAS 55610-02-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 321.33 g/mol
Formula C₁₉H₁₅NO₄
thermostat Physical Properties
Melting Point 266-270 °C
Boiling Point 573.9±60.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Cepharadione B is primarily studied for its potential biological activities, particularly in the field of anti-inflammatory and anticancer research. It has shown inhibitory effects on certain pro-inflammatory mediators, making it a candidate for development in treating inflammatory diseases. Additionally, it exhibits cytotoxic activity against various cancer cell lines, suggesting its role as a lead compound in anticancer drug discovery. Its natural origin and unique diterpenoid structure contribute to its pharmacological interest, especially in exploring new therapeutic agents from plant sources.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿60,560.00

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Cepharadione B
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Cepharadione B is primarily studied for its potential biological activities, particularly in the field of anti-inflammatory and anticancer research. It has shown inhibitory effects on certain pro-inflammatory mediators, making it a candidate for development in treating inflammatory diseases. Additionally, it exhibits cytotoxic activity against various cancer cell lines, suggesting its role as a lead compound in anticancer drug discovery. Its natural origin and unique diterpenoid structure contribute to i

Cepharadione B is primarily studied for its potential biological activities, particularly in the field of anti-inflammatory and anticancer research. It has shown inhibitory effects on certain pro-inflammatory mediators, making it a candidate for development in treating inflammatory diseases. Additionally, it exhibits cytotoxic activity against various cancer cell lines, suggesting its role as a lead compound in anticancer drug discovery. Its natural origin and unique diterpenoid structure contribute to its pharmacological interest, especially in exploring new therapeutic agents from plant sources.

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