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Art. -Nr.: HY-N17467

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Forsydoitriside A

Forsydoitriside A is an iridoid glycoside trimer found in the fruits of Forsythia suspensa. Forsydoitriside A shows no significant hepatoprotective activity against Acetaminophen (HY-66005)-induced damage in liver cells at 10 μM.

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CAS. Nr.: 2161432-06-8
Formel: C₄₈H₆₈O₂₈
Molecular Weight:1093.04

Speicherung:

Please store the product under the recommended conditions in the Certificate of Analysis.

Data Sheet (272 KB)

Forsydoitriside A Chemical Structure

CAS. Nr.: 2161432-06-8

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Biologische Aktivität
- Beschreibung
- In Vitro
Chemical Information
Reinheit & Dokumentation
Verweise
Calculators
Help & FAQs
Classifications
Bioz

Biologische Aktivität

Beschreibung

In Vitro

Forsydoitriside A (10 μM; 48 h) does not exhibit significant hepatoprotective activity against Acetaminophen-induced HepG2 cell damage, as indicated by its 50.86% cell survival rate^[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Cell Viability Assay^[1]

Cell Line:

HepG2
Concentration:

10 μM
Incubation Time:

48 h
Result:

Resulted in a cell survival rate of 50.86% in Acetaminophen-damaged HepG2 cells.

Chemical Information

CAS. Nr. 2161432-06-8
Molecular Weight 1093.04
Formel C₄₈H₆₈O₂₈
SMILES

OC(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
Structure Classification
- Saccharides
- Polysaccharides
Initial Source
Versand

Room temperature in continental US; may vary elsewhere.
Speicherung

Please store the product under the recommended conditions in the Certificate of Analysis.

Reinheit & Dokumentation

Select Batch:

Reinheit: 99.98%

Assay: 99.98%

ee.: 99.98%

Data Sheet (272 KB)
COA (2659 KB)
Elemental Analysis Report (2659 KB)
HNMR (2659 KB)
CNMR (2659 KB)
RP-HPLC (2659 KB)
NP-HPLC (2659 KB)
MS (2659 KB)
LCMS (2659 KB)
IR (2659 KB)
GC (2659 KB)
OR (2659 KB)
SDS-PAGE (2659 KB)
SEC-HPLC (2659 KB)
Other Report (2659 KB)
Handling Instructions (2659 KB)

Verweise

[1]. Shao SY, et al. New iridoid glycosides from the fruits of Forsythia suspensa and their hepatoprotective activities. Bioorg Chem. 2017;75:303-309. [Content Brief]

Calculators

Molaritätsrechner

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Mass Mass

Konzentration Konzentration

Volumen Volumen

Molecular Weight Molecular Weight

Verdünnungsrechner

Konzentration _{(Stammlösung)} × Volumen _{(Stammlösung)} = Konzentration _{(Ziellösung)} × Volumen _{(Ziellösung)}

Konzentration _{(Stammlösung)} Konzentration _{(Stammlösung)}

Volumen _{(Stammlösung)} Volumen _{(Stammlösung)}

Konzentration _{(Ziellösung)} Konzentration _{(Ziellösung)}

Volumen _{(Ziellösung)} Volumen _{(Ziellösung)}

Help & FAQs

How should lyophilized recombinant proteins be reconstituted and stored?

1. Before opening the cap, centrifuge the vial at 13000 rpm for 20-30 seconds. This step will ensure that any lyophilized powder that may have adhered to the cap or walls is collected at the bottom of the vial, minimizing the risk of product loss.

Keywords

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100 mg

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