Paeonolide
Paeonolide is a natural product from Paeonia lactiflora Pall.
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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.
Current Enzyme Inhibition2023, 19(1):55-64(10)
Vietnam Journal of Science2022,64(2):69-75.
J Sep Sci.2018, 41(11):2488-2497
Eur J Ther.2023, 29(4):900-906.
Acta Pharmaceutica Hungarica2016, 86:35-40
Sci Rep.2018, 8(1)
Eur J Pharmacol.2022, 917:174744.
Processes2023, 11(2), 385ĄŁ
J.Korean Society of Grassland&Forage Science2023, 43(3):138-147.
Food Sci Biotechnol.2023, 32(7):997-1003.
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Arch Pharm Res. 2001 Apr;24(2):105-8.
A new antioxidant monoterpene glycoside, alpha-benzoyloxypaeoniflorin from Paeonia suffruticosa.[Pubmed:
11339628]
METHODS AND RESULTS:
Alpha-benzoyloxypaeoniflorin (1), a new antioxidant monoterpene alpha-glycoside anomer was isolated from Paeonia suffruticosa along with known compounds, beta-benzoyloxypaeoniflorin (2), Paeonolide, paeoniflorin and mudanpioside H. The structure of 1 has been determined by comparing spectral data with those of beta-benzoyloxypaeoniflorin (2).
CONCLUSIONS:
Compound 1 exhibited moderately potent radical scavenging activity on DPPH radical.
