Ilexhainanoside D
Ilexhainanoside D is a natural product from Periploca sepiumBge.
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.
University of Burgos2024, ssrn.4795441.
Molecules.2021, 26(4):816.
Front Plant Sci.2018, 9:1424
Journal of Apiculture2019, 34(2):131-136
Biol Pharm Bull.2023, 46(2):245-256.
BMC Plant Biol.2018, 18(1):122
Eur J Pharmacol.2024, 975:176644.
Front Neurosci.2019, 13:1091
Appl Microbiol Biotechnol.2024, 108(1):207.
Food and Fermentation Industries2018, 44(371)
Related and Featured Products
Magn Reson Chem. 2009 Feb;47(2):169-73.
Complete assignments of 1H and 13C NMR spectral data for three new triterpenoid saponins from Ilex hainanensis Merr.[Pubmed:
18942070 ]
METHODS AND RESULTS:
Three new oleanane-type triterpenoid saponins, ilexhainanoside C, Ilexhainanoside D and ilexhainanoside E, all with 24, 28-dioic acid groups, were isolated from the leaves of Ilex hainanensis. They were 3beta-hydroxyolean-12-ene-24, 28-dioic acid-28-O-beta-D-glucopyranoside(1), 3beta, 19alpha-dihydroxyolean-12-ene-24, 28-dioic acid-28-O-beta-D-glucopyranoside(2) and 3beta, 29-dihydroxyolean-12-ene-24, 28-dioic acid-28-O-beta-D-glucopyranoside(3).
CONCLUSIONS:
The structures of these three new compounds were elucidated and complete assignments of the (1)H and (13)C NMR spectroscopic data were achieved by 1D and 2D NMR experiments [heteronuclear single quantum coherence (HSQC), HMBC and rotational nuclear Overhauser effect spectroscopy (ROESY)].
