Erythroskyrin

Erythroskyrin
Product Name Erythroskyrin
CAS No.: 4987-27-3
Catalog No.: CFN00116
Molecular Formula: C26H33NO6
Molecular Weight: 455.55 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: From Penicillium islandicum
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Erythroskyrin is a kind of mycotoxin.
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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.
  • Nutrients.2024, 16(7):965.
  • Molecules.2017, 22(2)
  • Chinese Journal of Hospital Pharmacy2020, 40(7)
  • Hindawi J of Food Biochemistry2023, P17:8883860
  • Asian Journal of Chemistry2018, 30(12):2699-2703
  • BMC Complement Med Ther. 2020, 20(1):94.
  • BMC Complement Altern Med.2016, 16:213
  • Pharmaceutics.2021, 13(7):1028.
  • Pharmaceuticals (Basel).2024, 17(3):352.
  • Biochem Pharmacol.2023, 211:115502.
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    J Nat Prod. 1988 May-Jun;51(3):562-6.
    Absolute and relative configuration of erythroskyrin.[Pubmed: 3404152]

    METHODS AND RESULTS:
    We have reisolated Erythroskyrin from Penicillium islandicum and have determined the relative stereochemistry of the compound through extensive 1H- and 13C-nmr studies.
    CONCLUSIONS:
    The absolute stereochemistry was determined by nmr studies of the O-methylmandelate esters.
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