Podophyllotoxinone
Podophyllotoxinone shows inhibitory activity against L1210 leukemia and KB cells in vitro.
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.
Foods.2020, 9(10):1348.
Phytomedicine.2023, 120:155063.
The Journal of Korean Medicine2023, 44(4):26-40.
Eur J Pharm Sci.2016, 94:33-45
Biotechnology and Bioprocess Engineering2024, 29:1048-1060.
Polytechnic University of Catalonia2017, 105826
Mol Biol Rep.2024, 51(1):117.
Phytomedicine.2020, 79, 153351
Clin Exp Pharmacol Physiol.2015, 42(11):1189-97
J. of Agricultural Science2015, 1916-9760
Related and Featured Products
Chinese Journal of Pharmaceuticals, 1993.
SYNTHESIS AND ANTITUMOR ACTIVITY OF PODOPHYLLOTOXINONE AND ITS HYDROXYIMINO ANALOGUES[Reference:
WebLink]
METHODS AND RESULTS:
Podophyllotoxinone and its hydroxyimino analogues have been synthesized by oxidation and oximation.
CONCLUSIONS:
The results of their inhibitory activities against L1210 leukemia and KB cells in vitro indicated that they were generally weaker than that of etoposide.
