Epischisandrone

Epischisandrone
Product Name Epischisandrone
CAS No.: 98619-26-2
Catalog No.: CFN95212
Molecular Formula: C21H24O5
Molecular Weight: 356.4 g/mol
Purity: >=98%
Type of Compound: Lignans
Physical Desc.: Powder
Source: The fruits of Schisandra sphenanthera
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price: $413/5mg
Reference standards.
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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.
  • Vietnam Journal of Food Control2022, 5(3):pp.390-401.
  • Cell Chem Biol.2019, 26(1):27-34
  • Plant Sci.2021, 313:111069.
  • Phytochem Anal.2013, 24(5):493-503
  • Chemistry of Natural Compounds2018, 204-206
  • Front Pharmacol.2018, 9:236
  • J. of Med. Plant Research.2013, 90-151
  • Environ Toxicol.2020, doi: 10.1002
  • Evid Based Complement Alternat Med.2020, 2020:1970349.
  • Pharmacol Rep.2020, 72(2):472-480.
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    The diethyl ether extract of the stems of Schisandra pubescens Hemsl. et Wils. (Schisandraceae) was found to exhibit cytotoxic activity in vitro. However, investigations of the bioactive constituents of this plant have been very limited. Elucidation of the cytotoxic constituents of S. pubescens was performed.
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    The structures of the new compounds were elucidated based on the spectral analysis, including 1D and 2D NMR experiments.
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