21-Episerratriol
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.
Appl. Sci.2020, 10,1304
Environ Toxicol.2020, doi: 10.1002
Food Res Int.2020, 128:108778
Chem Biol Interact.2024, 394:110995.
Oxid Med Cell Longev.2022, 2022:5888636.
Eur J Pharmacol.2024, 981:176883.
J Sep Sci.2020, 43(22):4148-4161.
Chemistry of Vegetable Raw Materials2019, 3:119-127
Cells.2021, 10(11):2919.
Chem Biol Interact.2022, 368:110248.
Related and Featured Products
Chemical & pharmaceutical bulletin.1974 Oct 25;22(10),2383-2395.
Triterpenoid Chemistry. VI. Lycopodium Triterpenoid. (5). The Structures and Stereochemistry of Serratriol, 21-Episerratriol, and Lycoclavanol.[Reference:
WebLink]
METHODS AND RESULTS:
The structures of triterpenoid-triols, serratriol, 21-Episerratriol, and lycoclavanol, isolated from Lycopodium plants, were established as serrat-14-en-3β, 21α, 24-triol (3), serrat-14-en-3β, 21β, 24-triol (36), and serrat-14-en-3α, 21β, 24-triol (22), respectively. The fourth possible stereoisomeric triol, serrat-14-en-3α, 21α, 24-triol (43), was prepared from lycoclavanol. New method of acetonide formation of 1,3-glycol was reported.
Australian Journal of Chemistry.1998;51(2):175-176.
Two New Abietanes from Lycopodium deuterodensum.[Reference:
WebLink]
METHODS AND RESULTS:
Two new abietanes, 6,11,14-trihydroxy-12-methoxyabieta-5,8,11,13-tetraene-3,7-dione (lycopod-abietane A) and 6,11,14-trihydroxy-12-methoxy-3α,18-cycloabieta-5,8,11,13-tetraen-7-one (lycopod-abietane B), were isolated from Lycopodium deuterodensum together with lycopodine, α-onocerin, 21-episerratenediol, 21-Episerratriol and 16-oxoserratenediol.
