Cucurbitacin S

Cucurbitacin S
Product Name Cucurbitacin S
CAS No.: 60137-06-6
Catalog No.: CFN90535
Molecular Formula: C30H42O6
Molecular Weight: 498.65 g/mol
Purity: >=98%
Type of Compound: Triterpenoids
Physical Desc.: Powder
Targets: Immunology & Inflammation related
Source: The rhizomes of Hemsleya amabilis Diels.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Cucurbitacins from Wilbrandia ebracteata have analgesic effects. Cucurbitacin S has anticancer and antiinflammatory activities.
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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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  • Acta Pharmaceutica Hungarica2016, 86:35-40
  • Life Sci.2021, 270:119074.
  • Phytomedicine.2019, 57:95-104
  • Daru.2024, 32(2):689-703.
  • Pharm Biol.2016, 54(7):1255-62
  • Patanjali Research Foundation2024, ssrn.4807357
  • International J of Green Pharmacy2019, 13(3)
  • Pharmaceutics.2020, 12(9):845.
  • Adaptive Medicine 2020, 12(1): 4-10
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    Phytochemistry Volume 21, Issue 11, 1982, Pages 2703–2707
    A revision of the structure of cucurbitacin S from Bryonia dioica[Reference: WebLink]
    1H NMR studies at 400 MHz on Cucurbitacin S and its derivatives suggest that the structure of Cucurbitacin S previously isolated from Bryonia dioica should be revised from (22S)-22, 25-anhydro-2,16α,22,25-tetrahydroxy-3,11,23-trioxo-cucurbita-1,5-diene to (24S)-16,24-anhydro- 2,16α,24,25-tetrahydroxy-3,11,22-trioxo-cucurbita-1,5-diene.
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