Sissotrin

Sissotrin
Product Name Sissotrin
CAS No.: 5928-26-7
Catalog No.: CFN97005
Molecular Formula: C22H22O10
Molecular Weight: 446.4 g/mol
Purity: >=98%
Type of Compound: Flavonoids
Physical Desc.: Yellow powder
Source: The herbs of Trifolium pratense L.
Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
Price: $268/5mg
Sissotrin can impair glucose tolerance.
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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.
  • Heliyon.2022, 8(12):e12031.
  • Int J Mol Sci.2024, 25(12):6456.
  • Molecules.2024, 29(5):1171.
  • J of Applied Pharmaceutical Science2020, 10(1):077-082
  • Anal Biochem.2019, 569:10-15
  • Toxicol In Vitro.2022, 81:105346.
  • Int J Biol Macromol.2020, 161:1230-1239.
  • Chulalongkorn University2024, 4761190
  • bioRxiv - Biochemistry2023, 548213.
  • Molecules.2023, 28(3):958.
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    The opposing effects of the flavonoids isoquercitrin and sissotrin, isolated from Pterospartum tridentatum, on oral glucose tolerance in rats.[Pubmed: 18338765]

    METHODS AND RESULTS:
    The isoflavone Sissotrin and the flavonol derivative, isoquercitrin, were selected for the oral glucose tolerance test. Isoquercitrin (100 mg/kg) showed time-dependent antihyperglycaemic activity by delaying the post-oral glucose load glycaemic peak at 30 min, as did the sodium-dependent glucose transporter inhibitor phloridzin (100 mg/kg). In contrast, Sissotrin (100 mg/kg) showed an opposite effect, impairing glucose tolerance.
    CONCLUSIONS:
    In conclusion, these preliminary results indicate that the effect of the extract on blood glucose may be either antihyperglycaemic or hyperglycaemic. Additionally, as far as is known, these are the first in vivo results on the acute antihyperglycaemic potential of isoquercitrin.
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