Mannioside A

Mannioside A
Product Name Mannioside A
CAS No.: 1038922-95-0
Catalog No.: CFN99055
Molecular Formula: C39H62O13
Molecular Weight: 738.9 g/mol
Purity: >=98%
Type of Compound: Steroids
Physical Desc.: Powder
Targets: Immunology & Inflammation related
Source: The herbs of Dracaena mannii
Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
Price:
Mannioside A has anti-inflammatory activity, inhibits carrageenan-induced paw edema in the rat.
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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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    CAS No: 1038922-95-0
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    Arch Pharm Res. 2008 May;31(5):653-8.
    In vivo anti-inflammatory effect of a new steroidal saponin, mannioside A, and its derivatives isolated from Dracaena mannii.[Pubmed: 18481024]

    METHODS AND RESULTS:
    A new steroidal saponin, Mannioside A (1), was isolated from the stem bark of Dracaena mannii, together with the known pennogenin (2), pennogenin-3-O-beta-D-glucopyranoside (3) and pennogenin-3-O-alpha-L-rhamnopyranosyl-(1-->2)-[alpha-L-rhamnopyranosyl-(1-->3)]-beta-D-glucopyranoside (4). Their structures were determined using 1D-and 2D-NMR spectroscopy and mass spectrometry.
    CONCLUSIONS:
    Compounds 1 and 3 significantly inhibited carrageenan-induced paw edema in the rat; compound 4 was moderately active whereas 2 showed very weak activity.
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