Jatamanvaltrate B

Jatamanvaltrate B
Product Name Jatamanvaltrate B
CAS No.: 1134138-66-1
Catalog No.: CFN96826
Molecular Formula: C32H50O13
Molecular Weight: 642.73 g/mol
Purity: >=98%
Type of Compound: Iridoids
Physical Desc.: Oil
Source: The whole plants of Valeriana jatamansi.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Jatamanvaltrate B shows cytotoxicity against lung adenocarcinoma (A549), metastatic prostate cancer (PC-3M), colon cancer (HCT-8),and hepatoma (Bel7402) 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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    J Nat Prod. 2009 Apr;72(4):650-5.
    Acylated iridoids with cytotoxicity from Valeriana jatamansi.[Pubmed: 19245261 ]
    Thirteen new acylated iridoids, jatamanvaltrate A, Jatamanvaltrate B, jatamanvaltrate C, jatamanvaltrate D, jatamanvaltrate E, jatamanvaltrate F, jatamanvaltrate G, jatamanvaltrate H, jatamanvaltrate I, jatamanvaltrate J, jatamanvaltrate K, jatamanvaltrate L, jatamanvaltrate M (1-13), together with nine known valepotriates (14-22), were isolated from the whole plants of Valeriana jatamansi (syn. Valeriana wallichii).
    METHODS AND RESULTS:
    The structures of these new compounds were assigned by detailed interpretation of spectroscopic data. Jatamanvaltrates D (4) and H (9) are the first examples of naturally occurring valepotriates containing an o-hydroxybenzoyloxy moiety at C-10. All isolated compounds were tested for their cytotoxicity against lung adenocarcinoma (A549), metastatic prostate cancer (PC-3M), colon cancer (HCT-8), and hepatoma (Bel7402) cell lines.
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