Tenacissoside F

Tenacissoside F
Product Name Tenacissoside F
CAS No.: 928151-78-4
Catalog No.: CFN97496
Molecular Formula: C35H56O12
Molecular Weight: 668.8 g/mol
Purity: >=98%
Type of Compound: Steroids
Physical Desc.: Powder
Source: The herbs of Marsdenia tenacissima
Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
Price:
Standard reference
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Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
  • Front Pharmacol.2021, 12:652860.
  • Phytochem Anal.2023, pca.3305.
  • Anticancer Res.2022, 42(9):4403-4410.
  • Molecules.2023, 28(9):3685.
  • Sci Rep.2017, 7(1):3249
  • Ulm University Medical Center2020, doi: 10.18725.
  • bioRxiv2021, 462065.
  • Food Res Int.2022, 157:111397.
  • J AOAC Int.2023, 106(1):56-64.
  • PLoS One.2017, 12(8):e0181191
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    METHODS AND RESULTS:
    A sensitive and specific liquid chromatography tandem mass spectrometry (LC-MS/MS) method was developed and validated the first time for simultanenous determination of three isomeric pregnane genins (17β-tenacigenin B, tenacigenin B and tenacigenin A) and their corresponding glycosides (tenacigenoside A, Tenacissoside F and marsdenoside I) from XAPI in rat plasma. The method showed satisfactory linearity over a concentration range 5.00-2000.00 ng/mL for tenacigenin B, tenacigenin A, marsdenoside I and Tenacissoside F (r(2) > 0.99), 10.00-4000.00 ng/mL for 17β-tenacigenin B and tenacigenoside A (r(2) > 0.99). Intra- and inter-day precisions (valued as relative standard deviation) were <9.00% and accuracies (as relative error) in the range -6.31 to 7.23%.
    CONCLUSIONS:
    Finally, this validated method was successfully applied to the pharmacokinetic study of XAPI after intravenous administration to rats.
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