Lucyoside B

Lucyoside B
Product Name Lucyoside B
CAS No.: 91174-19-5
Catalog No.: CFN90905
Molecular Formula: C42H68O15
Molecular Weight: 812.99 g/mol
Purity: >=98%
Type of Compound: Triterpenoids
Physical Desc.: Powder
Source: The herbs of Luffa cylindrica ROEM.
Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
Price: $388/5mg
Lucyoside B is a natural product from Luffa cylindrica ROEM.
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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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    Yakugaku Zasshi Journal of the Pharmaceutical Society of Japan, 1984, 104(3):246.
    Studies on the Constituents of Cucurbitaceae Plants. VI. On the Saponin Constituents of Luffa cylindrica ROEM.(1) [Reference: WebLink]

    METHODS AND RESULTS:
    New saponins, named lucyoside A (1),Lucyoside B (2), lucyoside C (3), lucyoside D (4), lucyoside E (5), lucyoside F (6),lucyoside G (7),lucyoside H (8), besides known ginsenosides-Re (9) and -Rg_1 (10), were isolated from herb of Luffa cylindrica ROEM.. On methanolysis 1,2,3,5,7 and 8 yielded methyl 21β-hydroxyhederagenin (11), arjunolic acid (12), methyl machaerinate (13), hederagenin (14), maslinic acid (15) and oleanolic acid (17), respectively.
    CONCLUSIONS:
    The structures of 1-8 were elucidated mainly mass, ^<13>C-nuclear magnetic resonance and ^1H-nuclear magnetic resonance spectroscopy.
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