Ferulamide

Ferulamide
Product Name Ferulamide
CAS No.: 61012-31-5
Catalog No.: CFN97041
Molecular Formula: C10H11NO3
Molecular Weight: 193.2 g/mol
Purity: >=98%
Type of Compound: Phenylpropanoids
Physical Desc.: Powder
Targets: PAFR
Source: The fruits of Croton tiglium
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Ferulamide derivatives show potent inhibitory activity against arachidonic acid-induced platelet aggregation.
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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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  • Hong Kong Baptist University2023, 048330T.
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  • Bulletin of Health Research2016, 44(4):279-286
  • J Chromatogr A.2017, 1518:46-58
  • Sci Rep.2020, 10:4495(2020)
  • Molecules.2023, 28(8):3376.
  • TCI CO.2019, US20190151281A1
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    Synthesis and anti-platelet activity of ferulamide derivatives[Reference: WebLink]

    METHODS AND RESULTS:
    A series of Ferulamide derivatives were prepared and evaluated for their anti-platelet activities. Some of these compounds showed potent inhibitory activity against arachidonic acid-induced platelet aggregation. Their structure-activity relationships are also discussed.
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