Trillenoside A

Trillenoside A
Product Name Trillenoside A
CAS No.: 58809-09-9
Catalog No.: CFN93326
Molecular Formula: C47H70O24
Molecular Weight: 1019.05 g/mol
Purity: >=98%
Type of Compound: Steroids
Physical Desc.: Powder
Targets: COX
Source: The herbs of Trillium tschonoskii Maxim.
Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
Price:
Trillenoside A displayed marked inhibitory action towards COX-2 production in macrophagocytes of the mouse abdominal cavity stimulated by LPS at 10 microg/ml.
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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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    Chem Pharm Bull (Tokyo). 2007 Apr;55(4):679-81.
    An 18-norspirostanol saponin with inhibitory action against COX-2 production from the underground part of Trillium tschonoskii.[Pubmed: 17409572 ]

    METHODS AND RESULTS:
    A novel 18-norspirostanol saponin (1), along with Trillenoside A (2), was obtained from the underground parts of Trillium tschonoskii MAXIM., collected in Shennongjia Forest District, China.
    CONCLUSIONS:
    Based on the chemical and spectroscopic evidences, their structures were determined as shown in Fig. 1. 1 and 2 displayed marked inhibitory action towards COX-2 production in macrophagocytes of the mouse abdominal cavity stimulated by LPS at 10 microg/ml.
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