F1839-I
F1839-I is a natural product from Stachybotrys sp.
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.
Food Analytical Methods2020, 13,1603-1612(2020)
Evid Based Complement Alternat Med.2018, 2018:8565132
Int J Nanomedicine.2024, 19:1683-1697.
Int J Oncol.2019, 55(1):320-330
The Japan Society for Analy. Chem.2017, 66(8):613-617
Anat Rec2018, 24264
Current Topics in Nutraceutical Research2021, 19(1),p90-105.
Metabolites.2023, 13(6):689.
J Agric Food Chem.2018, 66(1):351-358
Pharmaceuticals (Basel).2022, 15(5):591.
Related and Featured Products
Org Biomol Chem. 2016 Dec 20;15(1):65-68.
Enantiospecific total syntheses of meroterpenoids (-)-F1839-I and (-)-corallidictyals B and D.[Pubmed:
27853800 ]
Enantiospecific total syntheses of spiromeroterpenoid natural products (-)-F1839-I and (-)-corallidictyals B and D were achieved using the environmentally benign and highly atom economical Lewis acid catalysed Friedel-Crafts reaction and a highly regio- and stereoselective spirocyclic C-O bond formation reaction.
