Viscidulin III tetraacetate

96%

Reagent Code: #245410
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CAS Number 96684-81-0

science Other reagents with same CAS 96684-81-0

blur_circular Chemical Specifications

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Weight 514.45 g/mol
Formula C₂₅H₂₂O₁₂
inventory_2 Storage & Handling
Storage 2-8℃, dry, closed

description Product Description

Used in research for its potential anti-inflammatory and antioxidant properties. Shows activity in inhibiting certain enzymes involved in inflammatory pathways, making it of interest in developing treatments for chronic inflammatory conditions. Also studied for its ability to scavenge free radicals, which may contribute to cellular protection and reduced oxidative stress. Investigated for possible anticancer applications due to its effects on cell proliferation and apoptosis in preliminary in vitro studies. Primarily utilized as a biochemical tool in laboratory settings to understand flavonoid metabolism and structure-activity relationships.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿28,290.00

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Viscidulin III tetraacetate
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Used in research for its potential anti-inflammatory and antioxidant properties. Shows activity in inhibiting certain enzymes involved in inflammatory pathways, making it of interest in developing treatments for chronic inflammatory conditions. Also studied for its ability to scavenge free radicals, which may contribute to cellular protection and reduced oxidative stress. Investigated for possible anticancer applications due to its effects on cell proliferation and apoptosis in preliminary in vitro studi

Used in research for its potential anti-inflammatory and antioxidant properties. Shows activity in inhibiting certain enzymes involved in inflammatory pathways, making it of interest in developing treatments for chronic inflammatory conditions. Also studied for its ability to scavenge free radicals, which may contribute to cellular protection and reduced oxidative stress. Investigated for possible anticancer applications due to its effects on cell proliferation and apoptosis in preliminary in vitro studies. Primarily utilized as a biochemical tool in laboratory settings to understand flavonoid metabolism and structure-activity relationships.

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