Odonicin
Standard reference
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.
Materials Today Communications2023, 37:107216
J Pharmaceut Biomed2020, 178:112894
Chem Biol Interact.2020, 328:109200.
Plant Physiol.2024, 194(4):2580-2599.
Int J Mol Sci.2024, 25(22):12152.
Toxicol Mech Methods.2021, 1-12.
Int J Mol Sci.2019, 20(9):E2244
Saudi Pharmaceutical Journal2023, 31(12):101829
Pol J Microbiol.2021, 70(1):117-130.
Int J Mol Sci.2021, 22(12):6466.
Related and Featured Products
Fitoterapia. 2003 Jul;74(5):435-8.
Diterpenoids from Isodon japonica.[Pubmed:
12837357 ]
METHODS AND RESULTS:
A new ent-kaurane diterpenoid maoyecrystal F (1) and its acetonide derivative (2), together with seven known compounds, lasiodonin, maoyerabdosin, Odonicin, enmenin, oridonin, beta-sitosterol and daucosterol, were isolated from the leaves of Isodon japonica.
Journal of the Chemical Society Perkin Transactions 1, 01/1973.
Terpenoids. Part XXV. Structures and absolute configurations of isodoacetal, nodosinin, and odonicin, novel diterpenoids of Isodon japonicus[Reference:
WebLink]
METHODS AND RESULTS:
On the basis of spectroscopic data and chemical evidence, the structure and absolute configuration of isodoacetal (1a), nodosinin (6), and Odonicin (11) have been established. The first two are B-secokaurene derivatives and the third is ent-6α, 15α-diacetoxy-7β,20-epoxy-7α-hydroxykaura-2,16-dien-1-one. Chemical interconversions between isodoacetal and nodosinin have been accomplished.
