Cucurbitacin B 2-O-beta-D-glucoside

Cucurbitacin B 2-O-beta-D-glucoside
Product Name Cucurbitacin B 2-O-beta-D-glucoside
CAS No.: 65247-27-0
Catalog No.: CFN92141
Molecular Formula: C38H56O13
Molecular Weight: 720.9 g/mol
Purity: >=98%
Type of Compound: Triterpenoids
Physical Desc.: Powder
Source: The rhizomes of Hemsleya amabilis Diels.
Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
Price:
Cucurbitacin B 2-o-β-D-glucoside has anticancer activity.
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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.
  • J Microbiol Biotechnol.2020, 30(2):178-186.
  • Front Immunol.2024, 15:1423776.
  • Int J Biol Sci.2023, 19(10):3077-3098.
  • Int J Mol Sci.2024, 25(5):2914.
  • J Chromatogr Sci.2015, 53(5):824-9
  • Pharmaceutics2022, 14(2),376.
  • Trop J Nat Prod Res, February2023, 7(2):2371-2381
  • Food Control2022, 132:108434.
  • Phytomedicine.2019, 62:152962
  • Life Sci.2018, 209:498-506
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    Bioprocess Biosyst Eng. 2016 Sep;39(9):1435-40.
    A biotransformation process for the production of cucurbitacin B from its glycoside using a selected Streptomyces sp.[Pubmed: 27145940 ]
    Cucurbitacin B (CuB) and its glycoside, Cucurbitacin B 2-O-beta-D-glucoside (CuBg), abundantly occur in the pedicels of Cucumis melo. Compared with CuB, CuBg is not efficiently extracted from the pedicels. Furthermore, the anticancer activity of CuBg is lower than that of the aglycone.
    METHODS AND RESULTS:
    A process for CuBg biotransformation to CuB was developed for the first time. A strain of Streptomyces species that converts CuBg into CuB was isolated from an enrichment culture of C. melo pedicels. After optimization of conditions for enzyme production and biotransformation, a maximum conversion rate of 92.6 % was obtained at a CuBg concentration of 0.25 g/L. When biotransformation was performed on C. melo pedicel extracts, the CuB concentration in the extracts increased from 1.50 to 3.27 g/L. The conversion rate was almost 100 %.
    CONCLUSIONS:
    The developed process may be an effective biotransformation method for industrial production CuB from C. melo pedicels for pharmaceuticals.
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