Momor-cerebroside I

Momor-cerebroside I
Product Name Momor-cerebroside I
CAS No.: 606125-07-9
Catalog No.: CFN97031
Molecular Formula: C48H93NO10
Molecular Weight: 844.3 g/mol
Purity: >=98%
Type of Compound: Cerebrosides
Physical Desc.: Powder
Source: The herbs of Sesamum indicum L
Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
Price:
Momor-cerebroside I is a natural product from Sesamum indicum L.
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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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    Arch Pharm Res. 2003 Feb;26(2):138-42.
    Cerebrosides from Longan Arillus.[Pubmed: 12643590]
    From the pulp of Euphoria longana (Longan Arillus), three cerebroside molecular species have been isolated.
    METHODS AND RESULTS:
    Six known cerebrosides, soyacerebrosides I and II, 1-O-beta-D-glucopyranosyl-(2S,3R,4E,8E)-2-(2'-lignoceroylamino)-4,8-octadecadiene-1,3-diol (longan cerebroside I) and its 8Z isomer (longan cerebroside II), Momor-cerebroside I, and phytolacca cerebroside, were identified as major components of these cerebroside molecular species. All the cerebrosides were shown to be a mixture of geometrical isomers (8E and 8Z) of sphingosine-type or phytosphingosine-type glucocerebrosides possessing 2-hydroxy fatty acids.
    CONCLUSIONS:
    The structures of these cerebrosides have been determined on the basis of chemical and spectroscopic evidence.
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