Calystegine A7

Calystegine A7
Product Name Calystegine A7
CAS No.: 197565-90-5
Catalog No.: CFN00167
Molecular Formula: C7H13NO3
Molecular Weight: 159.18 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: The leaves of Morus alba L.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Calystegine A7 is a glycosidase inhibitor.
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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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  • Vietnam Journal of Food Control2022, 5(3):pp.390-401.
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  • Journal of Apiculture2023.38(3):249-254.
  • Appl. Sci. 2021, 11(8),3437.
  • Antimicrob Agents Chemother.2020, AAC.01921-20.
  • J Ethnopharmacol.2022, 291:115159.
  • Appl. Sci. 2021, 11(23),11099.
  • J.of Traditional&Complementary Med.2022, 10.1016:j.jtcme.
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    Total synthesis of calystegine A7.[Reference: WebLink]

    METHODS AND RESULTS:
    A straightforward chiral pool synthesis for the glycosidase inhibitor Calystegine A7 (isolated from Lycium chinense) from methyl α-d-glucopyranoside is described. Keysteps of this synthesis include a ultrasound assisted Zn-mediated tandem ring opening reaction followed by a Grubbs' catalyst mediated ring closure metathesis.
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