Product Data Sheet

Forsydoitriside A

Catalog No. A95740

main product photo
Forsydoitriside A is an iridoid glycoside trimer extracted from the fruits of Forsythia suspensa. This compound is studied for its potential biological activities, although it has been shown to lack significant hepatoprotective effects against Acetaminophen-induced liver cell damage at a concentration of 10 μM. Research applications may explore its broader roles in pharmacology and its interactions in various biochemical pathways.
Chemical Information
Catalog NumA95740
M. Wt1093.04
FormulaC48H68O28
Purity>98%
Storageat -20 °C 3 years (powder form); at -20 °C 6 months (Solution base)
CAS No.2161432-06-8
Synonyms
SMILESOC(C1=CO[C@@H](O[C@@H]2O[C@@H]([C@H]([C@@H]([C@H]2O)O)O)CO)[C@]([C@]1([H])CC3)([H])[C@H]3COC(C4=CO[C@H]([C@@]5([H])[C@]4([H])CC[C@@H]5COC(C6=CO[C@@H](O[C@@H]7O[C@@H]([C@H]([C@@H]([C@H]7O)O)O)CO)[C@@]8([H])[C@]6([H])CC[C@@H]8CO)=O)O[C@@H]9O[C@@H]([C@H]([C@@H]([C@H]9O)O)O)CO)=O)=O
Biological Activity
DescriptionForsydoitriside A is an iridoid glycoside trimer extracted from the fruits of Forsythia suspensa. This compound is studied for its potential biological activities, although it has been shown to lack significant hepatoprotective effects against Acetaminophen-induced liver cell damage at a concentration of 10 μM. Research applications may explore its broader roles in pharmacology and its interactions in various biochemical pathways.
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SHIPPING AND STORAGE
Adooq products are transported at room temperature. If you receive the product at room temperature, please rest assured, the Adooq Quality Inspection Department has conducted experiments to verify that the normal temperature placement of one month will not affect the biological activity of powder products. After collecting, please store the product according to the requirements described in the datasheet. Most Adooq products are stable under the recommended conditions.