Kalopanaxsaponin G
Reference standards.
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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.
Antioxidants (Basel).2020, 9(4):284.
Int J Mol Sci.2019, 20(14):E3538
Analytical Methods2018, 10(27)
Pharmaceuticals (Basel).2024 Feb 24;17(3):292.
J Complement Integr Med.2024, jcim-2023-0177.
Applied Physics B2021, 127(92).
Toxicol In Vitro.2019, 59:161-178
Kor. J. Pharmacogn.2016, 47(1):62-72
United States Patent Application2020, 20200038363
Pharmaceutics.2023, 15(6):1771.
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J Nat Prod. 1999 Mar;62(3):445-8.
Triterpenoid saponins of Acanthopanax nipponicus leaves.[Pubmed:
10096855 ]
METHODS AND RESULTS:
Five new triterpenoid saponins, nipponosides A-E (1, 3-6), were isolated from Acanthopanax nipponicus leaves, along with a known saponin, Kalopanaxsaponin G (2). Nipponosides A-E were characterized as the 28-O-alpha-L-rhamnopyranosyl(1-->4)-beta-D-glucopyranosyl(1-->6)-beta -D-glucopyranosyl ester of 3-oxohederagenin, oleanolic acid 3-O-beta-D-glucopyranoside, gypsogenin 3-O-beta-D-glucopyranoside, 3beta,23,29-trihydroxyolean-12-en-28-oic acid, and 3beta,20alpha, 23-trihydroxy-30-nor-olean-12-en-28-oic acid, respectively.
CONCLUSIONS:
The structures of these new compounds were based on chemical and spectral methods.
