1,7-Bis(4-hydroxyphenyl)-3-hydroxy-1,3-heptadien-5-one

1,7-Bis(4-hydroxyphenyl)-3-hydroxy-1,3-heptadien-5-one
Product Name 1,7-Bis(4-hydroxyphenyl)-3-hydroxy-1,3-heptadien-5-one
CAS No.: 207792-17-4
Catalog No.: CFN96210
Molecular Formula: C19H18O4
Molecular Weight: 310.4 g/mol
Purity: >=98%
Type of Compound: Phenols
Physical Desc.: Yellow powder
Targets: PAFR
Source: The roots of Curcuma longa L.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
1,7-Bis(4-hydroxyphenyl)-3-hydroxy-1,3-heptadien-5-one shows strong inhibition of collagen-induced, arachidonic acid-induced, and adenosine diphosphate-induced platelet aggregation of human whole blood.
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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. 1998 Jan;61(1):142-4.
    A new antiplatelet diarylheptanoid from Alpinia blepharocalyx.[Pubmed: 9461664 ]

    METHODS AND RESULTS:
    A new diarylheptanoid, 1,7-Bis(4-hydroxyphenyl)-3-hydroxy-1,3-heptadien-5-one (1), along with seven other known compounds, were isolated from the seeds of Alpinia blepharocalyx.
    CONCLUSIONS:
    Of these, compounds 1 and 3 showed strong inhibition of collagen-induced, arachidonic acid-induced, and adenosine diphosphate-induced platelet aggregation of human whole blood. Compound 3 also strongly inhibited ristocetin-induced platelet aggregation. Structures of these compounds were elucidated by spectroscopic and chemical means.
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