Taxachitriene A

Taxachitriene A
Product Name Taxachitriene A
CAS No.: 167906-74-3
Catalog No.: CFN96644
Molecular Formula: C32H44O13
Molecular Weight: 636.69 g/mol
Purity: >=98%
Type of Compound: Diterpenoids
Physical Desc.: Powder
Source: The seeds of the Chinese yew Taxus chinensis.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Taxachitriene A is a natural product from the Chinese yew Taxus chinensis.
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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. 1999 Jan;62(1):149-51.
    New taxoids from the seeds of taxus chinensis.[Pubmed: 9917305 ]

    METHODS AND RESULTS:
    Two new taxoids, 2alpha-acetoxy-2',7-dideacetoxyaustrospicatine (1) and decinnamoyltaxinine E (2), have been isolated from the extracts of the seeds of the Chinese yew Taxus chinensis (Pilg.) Rehd. in addition to taxuspine Z (3), taxin B (4), taxezopidine G (5), 7, 2'-bisdeacetoxyaustropicatine (6), 5alpha-cinnamoyl-9alpha,10beta, 13alpha-triacetoxytaxa-4(20),11-diene (7), Taxachitriene A, 20-deacetylTaxachitriene A, 13-O-acetylbrevifoliol, taxinines A and J, and taxacin.
    CONCLUSIONS:
    The structures of these compounds were elucidated on the basis of spectral analysis and chemical derivatizations.
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