1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane
1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane is a natural product from Ligularia fischeri.
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.
J. Soc. Cosmet. Sci. Korea2016, 163-171
Int. J. Mol. Sci.2022, 23(8), 4130.
Antioxidants (Basel).2021, 10(11): 1802.
Journal of Apicultural Research2021, 60(1)
LWT2021, 150:112021.
Nat Prod Sci.2019, 25(3):238
Molecules.2019, 24(12):E2286
Molecules.2020 ,25(16):3697.
Arch Biochem Biophys.2020, 687:108384.
Int J Nanomedicine.2022, 17:6513-6525.
Related and Featured Products
J Nat Prod. 2010 Feb 26;73(2):143-6.
A pair of epimeric spirosesquiterpenes from the roots of Ligularia fischeri.[Pubmed:
20104879 ]
METHODS AND RESULTS:
Two new highly oxygenated spirosesquiterpene lactones, ligulactones A (1) and B (2), and one known sesquiterpenoid, 1beta,10beta-Epoxy-6beta-isobutyryloxy-9-oxofuranoeremophilane (3), were isolated from the roots of Ligularia fischeri. Their structures and relative configurations were elucidated by 1D and 2D NMR and MS data and by comparison of their NMR data with those of related compounds. Single-crystal X-ray diffraction analyses confirmed their structures.
CONCLUSIONS:
Compounds 1 and 2 are C-7 epimers. A possible biosynthetic process for their formation is proposed. Structure 3 was proposed as the likely parent compound for the two new epimeric sesquiterpenoids.
