Sessilifoline A
Sessilifoline A is a natural product from Stemona japonica.
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 Ethnopharmacol.2020, 249:112396
Heliyon.2023, e12684.
Cells.2021, 10(10):2633.
Korean Journal of Pharmacognosy.2020, 51(2):100-106
Food and Chemical Toxicology2020, 111221
Analytical Methods2018, 10(27)
J Bone Miner Res.2017, 32(12):2415-2430
Food Funct.2024, 15(8):4262-4275.
Acta Physiologiae Plantarum2016, 38:7
Journal of Food Hygiene and Safety2019, 34(5):413-420
Related and Featured Products
Helvetica Chimica Acta, 2007, 90:326-337.
Novel Alkaloids from Stemona sessilifolia[Reference:
WebLink]
METHODS AND RESULTS:
Two new alkaloids, Sessilifoline A ( 1 ) and sessilifoline B ( 2a ), were isolated from the stems of Stemona sessilifolia , together with three known alkaloids, tuberstemonine ( 3 ), sessilifoliamide A ( 4 ), and stemoninoamide ( 5 ).
CONCLUSIONS:
Their structures were established by mass-spectrometric and spectroscopic methods, especially 2D-NMR techniques.
