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5-O-Caffeoylshikimic acid

Catalog No. TN1295Cas No. 73263-62-4

5-O-Caffeoylshikimic acid shows anti-oxidative activity; it also shows anti-inflammatory activity, the underlying mechanism was associated with downregulation of nuclear factor-κB.

5-O-Caffeoylshikimic acid

5-O-Caffeoylshikimic acid

Purity: 99.82%
Catalog No. TN1295Cas No. 73263-62-4
5-O-Caffeoylshikimic acid shows anti-oxidative activity; it also shows anti-inflammatory activity, the underlying mechanism was associated with downregulation of nuclear factor-κB.
Pack SizePriceAvailabilityQuantity
1 mg$116In Stock
5 mg$282In Stock
10 mg$418In Stock
25 mg$695In Stock
50 mg$988In Stock
1 mL x 10 mM (in DMSO)$370In Stock
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Purity:99.82%
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Product Introduction

Bioactivity
Description
5-O-Caffeoylshikimic acid shows anti-oxidative activity; it also shows anti-inflammatory activity, the underlying mechanism was associated with downregulation of nuclear factor-κB.
In vitro
Cytotoxic activity of saponins and phenolic compounds have been described in the literature, but no reports were found on their multidrug resistance (MDR)-modulating effects on human mdr1 gene-transfected mouse lymphoma cell line.Methylprototribestin, structurally related compounds and a mixture of 3 acetylated isomers of methylprotodioscin were investigated for antiproliferative effect and modulation of drug accumulation. RESULTS: The growth inhibitory dose (ID50) of the compounds ranged from 12.64 to 20.62 mug/ml. Methylprototribestin was the most effective resistance modifier. However, methylprotodioscin, pseudoprotodioscin, prosapogenin A of dioscin, tribestin and 5-O-Caffeoylshikimic acid showed moderate MDR reversal activity. In a checkerboard method, methyloprototribestin and the mixture of the 3 acetylated isomers enhanced the antiproliferative effects on MDR cells in combination with doxorubicin. CONCLUSION: Based on these results, methylprototribestin and the mixture of the 3 acetylated isomers can be recommended for further in vivo experiments in combination with anthracyclines in human MDR-cancer xenograft transplanted mice[1]
Chemical Properties
Molecular Weight336.29
FormulaC16H16O8
Cas No.73263-62-4
Storage & Solubility Information
Storagekeep away from direct sunlight,store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 50 mg/mL (148.68 mM)
H2O: 20 mg/mL (59.47 mM), sonification is recommended.
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM2.9736 mL14.8681 mL29.7362 mL148.6812 mL
5 mM0.5947 mL2.9736 mL5.9472 mL29.7362 mL
10 mM0.2974 mL1.4868 mL2.9736 mL14.8681 mL
20 mM0.1487 mL0.7434 mL1.4868 mL7.4341 mL
50 mM0.0595 mL0.2974 mL0.5947 mL2.9736 mL
DMSO
1mg5mg10mg50mg
100 mM0.0297 mL0.1487 mL0.2974 mL1.4868 mL

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