Kalopanaxsaponin G
Reference standards.
Inquire / Order:
manager@chemfaces.com
Technical Inquiries:
service@chemfaces.com
Tel:
+86-27-84237783
Fax:
+86-27-84254680
Address:
1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
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.
Molecules.2019, 24(24),4583
J Biomol Struct Dyn.2023, 1-21.
BMC Complement Altern Med.2018, 18(1):221
Food Funct.2022, D1FO03838A.
Int J Mol Sci.2023, 24(8):7045.
J of the Korean Society of Cosmetics and Cosmetology2019, 225-231
Korean J of Food Science&Technology 2017, 49(2):146-150
Int J Mol Sci.2023, 25(1):283.
Ulm University Medical Center2020, doi: 10.18725.
Anal Chim Acta.2018, 1039:162-171
Related and Featured Products
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.
