Sendanolactone

Sendanolactone
Product Name Sendanolactone
CAS No.: 64929-59-5
Catalog No.: CFN97113
Molecular Formula: C30H42O4
Molecular Weight: 466.7 g/mol
Purity: >=98%
Type of Compound: Triterpenoids
Physical Desc.: Powder
Source: The barks of Melia azedarach
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Sendanolactone possesses moderate cytotoxic activity against KB cell lines.
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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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    METHODS AND RESULTS:
    Two new terpenoids, bakayanolide (1) and 2α-hydroxy-3β-methoxy-6-oxo-13α,14β,17α-lanosta-7,24-dien-21,16β-olide (2), together with the known compounds 6β-hydroxy-3-oxo-13α,14β,17α-lanosta-7,24-dien-21,16β-olide (3), Sendanolactone (4), kulactone (5), and β-sitosterol have been isolated from the ethanolic root extracts of Melia azedarach. Triterpenoids (4), (5), and β-sitosterol have been identified previously from M. azedarach, while it is the first instance of the isolation of (3) from this source. The identity of these compounds was established through extensive spectroscopic methods (infrared and mass spectroscopy, 1H and 13C nuclear magnetic resonance) as well as appropriate two-dimensional nuclear magnetic resonance experiments.
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