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Calenduloside E

🥰Excellent
Catalog No. TJS0928Cas No. 26020-14-4
Alias Silphioside F

Calenduloside E (Silphioside F) is a pentacyclic triterpene saponin extracted from Panax japonicus. It targets heat shock protein 90 (Hsp90) and has anti-apoptotic effect.

Calenduloside E

Calenduloside E

🥰Excellent
Purity: 98.99%
Catalog No. TJS0928Alias Silphioside FCas No. 26020-14-4
Calenduloside E (Silphioside F) is a pentacyclic triterpene saponin extracted from Panax japonicus. It targets heat shock protein 90 (Hsp90) and has anti-apoptotic effect.
Pack SizePriceUSA WarehouseGlobal WarehouseQuantity
1 mg$117In StockIn Stock
5 mg$289In StockIn Stock
10 mg$413In StockIn Stock
25 mg$688In StockIn Stock
50 mg$979In StockIn Stock
100 mg$1,320-In Stock
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In Stock Estimated shipping dateUSA Warehouse[1-2 days] Global Warehouse[5-7 days]
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Batch Information

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Purity:98.99%
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COA LCMS HNMR

Product Introduction

Bioactivity
Description
Calenduloside E (Silphioside F) is a pentacyclic triterpene saponin extracted from Panax japonicus. It targets heat shock protein 90 (Hsp90) and has anti-apoptotic effect.
SynonymsSilphioside F
Chemical Properties
Molecular Weight632.82
FormulaC36H56O9
Cas No.26020-14-4
Smiles[H][C@@]1(O[C@H]2CC[C@@]3(C)[C@@]([H])(CC[C@]4(C)[C@]3([H])CC=C3[C@]5([H])CC(C)(C)CC[C@@]5(CC[C@@]43C)C(O)=O)C2(C)C)O[C@@H]([C@@H](O)[C@H](O)[C@H]1O)C(O)=O
Relative Density.1.27 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Solubility Information
DMSO: 75 mg/mL (118.52 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM1.5802 mL7.9011 mL15.8023 mL79.0114 mL
5 mM0.3160 mL1.5802 mL3.1605 mL15.8023 mL
10 mM0.1580 mL0.7901 mL1.5802 mL7.9011 mL
20 mM0.0790 mL0.3951 mL0.7901 mL3.9506 mL
50 mM0.0316 mL0.1580 mL0.3160 mL1.5802 mL
100 mM0.0158 mL0.0790 mL0.1580 mL0.7901 mL

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Please enter your animal experiment information in the following box and click Calculate to obtain the mother liquor preparation method and in vivo formula preparation method:
TargetMol | Animal experimentsFor example, your dosage is 10 mg/kg Each animal weighs 20 g, and the dosage volume is 100 μL . TargetMol | Animal experiments A total of 10 animals were administered, and the formula you used is 5% TargetMol | reagent DMSO+30% PEG300+5% Tween 80+60% Saline/PBS/ddH2O. So your working solution concentration is 2 mg/mL。
Mother liquor preparation method: 2 mg of drug dissolved in 50 μL DMSOTargetMol | reagent (mother liquor concentration of 40 mg/mL), if you need to configure a concentration that exceeds the solubility of the product, please contact us first.
Preparation method for in vivo formula: Take 50 μL DMSOTargetMol | reagent main solution, add 300 μLPEG300TargetMol | reagent mix well and clarify, then add 50 more μL Tween 80, mix well and clarify, then add 600 more μLSaline/PBS/ddH2OTargetMol | reagent mix well and clarify
For Reference Only. Please develop an appropriate dissolution method based on your laboratory animals and route of administration.
All types of co-solvents required for the protocol, such asDMSO, PEG300/ PEG400, Tween 80, SBE-β-CD, corn oil are available for purchase on the TargetMol website with a simple click.
1 Enter information below:
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2 Enter the in vivo formulation:
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Keywords

InhibitorinhibitHSPHeat shock proteinsEndogenous MetaboliteCalenduloside E
Related Tags: buy Calenduloside E | purchase Calenduloside E | Calenduloside E cost | order Calenduloside E | Calenduloside E chemical structure | Calenduloside E formula | Calenduloside E molecular weight
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