Citrostadienol

Citrostadienol
Product Name Citrostadienol
CAS No.: 474-40-8
Catalog No.: CFN89063
Molecular Formula: C30H50O
Molecular Weight: 426.72 g/mol
Purity: >=98%
Type of Compound: Steroids
Physical Desc.: Powder
Source: The herbs of Prunus armeniaca L.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Citrostadienol shows cytotoxic activity against B16F10 melanoma cells.
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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.
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  • Chem Biol Interact.2016, 258:59-68
  • J Ethnopharmacol.2023, 309:116302.
  • Phytomedicine.2022, 110:154597.
  • Institute of Food Science & Technology2021, 45(9).
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  • Phytother Res.2019, 33(7):1784-1793
  • Food Chem.2016, 191:81-90
  • Int J Mol Sci.2018, 19(9):E2601
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    J Ethnopharmacol. 2013 Oct 28;150(1):263-9.
    Antitumoural effect of Synadenium grantii Hook f. (Euphorbiaceae) latex.[Pubmed: 24008110]

    METHODS AND RESULTS:
    The Synadenium grantii latex exhibited decreased cell viability of the melanoma line in a concentration and time-dependent manner, and also cell cycle arrest in the S-G2/M phase. The latex caused a 40% reduction in the volume of tumours of the mice with melanomas. Histological examination of the organs of these animals showed no differences between groups. The phytochemical investigation resulted in the isolation and identification of triterpene euphol and the steroid Citrostadienol, which were tested against the strain of melanoma. Euphol showed no antitumoural activity, while the steroid Citrostadienol showed reduced cytotoxic activity.
    CONCLUSIONS:
    The Synadenium grantii latex presented in vitro and in vivo cytotoxic effects with antitumoural activity against B16F10 melanoma cells.
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