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Tenacissoside D

CAS# 107343-57-9

Tenacissoside D

2D Structure

Catalog No. BCX2204----Order now to get a substantial discount!

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Tenacissoside D: 5mg $200 In Stock
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Quality Control of Tenacissoside D

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Tenacissoside D

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Chemical Properties of Tenacissoside D

Cas No. 107343-57-9 SDF File under preparation.
PubChem ID N/A Appearance Powder
Formula C51H80O19 M.Wt 997.2
Type of Compound Steroids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Source of Tenacissoside D

The herbs of Marsdenia tenacissima

Tenacissoside D Dilution Calculator

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Tenacissoside D Molarity Calculator

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Preparing Stock Solutions of Tenacissoside D

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.0028 mL 5.014 mL 10.0281 mL 20.0562 mL 25.0702 mL
5 mM 0.2006 mL 1.0028 mL 2.0056 mL 4.0112 mL 5.014 mL
10 mM 0.1003 mL 0.5014 mL 1.0028 mL 2.0056 mL 2.507 mL
50 mM 0.0201 mL 0.1003 mL 0.2006 mL 0.4011 mL 0.5014 mL
100 mM 0.01 mL 0.0501 mL 0.1003 mL 0.2006 mL 0.2507 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on Tenacissoside D

Qualitative and quantitative analyses of chemical components in different parts of Marsdenia cavaleriei.[Pubmed:40311483]

J Chromatogr B Analyt Technol Biomed Life Sci. 2025 Jun 1;1259:124617.

Species of the genus Marsdenia have a long history of medicinal use in China, with C21 steroids serving as the principal bioactive constituents. Marsdenia cavaleriei remains an unexplored phytochemical resource, particularly regarding the material basis in different plant parts. In this study, an ultra-high-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (UHPLC-Q-TOF/MS) analytical method was developed to thoroughly characterize the chemical constituents of this plant. A total of 68 compounds were identified, 48 of which were tentatively identified as novel. Principal component analysis (PCA) and orthogonal partial least squares discriminant analysis (OPLS-DA) were employed to screen 18 potential chemical markers, elucidating compositional differences across various plant parts. Quantification of Tenacissoside H was conducted using ultra-high-performance liquid chromatography with charged aerosol detection (UHPLC-CAD), revealing its absence in the leaves. The average content of Tenacissoside H in the roots (0.281 %) exceeded that in the stems. A semi-quantitative analytical method was developed under identical gradient conditions with inverse gradient compensation. The relative standard deviation (RSD) of the average response factors for five references was 2.46 %. The semi-quantitative analysis of nine primary C21 steroids showed that Tenacigenoside K and Tenacissoside A were most abundant in the leaves, Tenacissoside A and Marsdenoside H dominated in the stems, and Marsdenoside H and Tenacissoside D were the most prevalent in the roots. This study presents a comprehensive approach for qualitative and quantitative analysis, thereby enhancing our understanding of the chemical composition of M. cavaleriei across its various parts and providing a foundation for its broader application.

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