Pachysamine M

Pachysamine M
Product Name Pachysamine M
CAS No.: 1253202-75-3
Catalog No.: CFN89007
Molecular Formula: C28H44N2O2
Molecular Weight: 440.67 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: The roots of Sarcococca ruscifolia.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Pachysamine M shows inhibitory activities against multiple types of cancer 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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    Pregnane alkaloids from Sarcococca ruscifolia and their cytotoxic activity. [Reference: WebLink]

    METHODS AND RESULTS:
    Six pregnane alkaloids were isolated from the root of Sarcococca ruscifolia. The structures of three new alkaloids, namely, sarcorucinine E-G (1-3), were elucidated using spectroscopic methods, while three known alkaloids, namely, epipachysamine D, Pachysamine M, and sarcovagine D, were identified by comparing their spectral data with those of the compounds reported earlier.
    CONCLUSIONS:
    All compounds were evaluated for their inhibitory activities against multiple types of cancer cells.
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