Prionoid E
Prionoid E (IC50 = 0.72 microM) shows significant cytotoxic activity against A-549 cell lines.
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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.
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Front Cell Dev Biol.2021, 9:588093.
Molecules2022, 27(9):2613.
J Nat Med.2018, 72(3):734-744
Recent Pat Anticancer Drug Discov.2022, 17(4):416-426.
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Planta Med. 2005 Sep;71(9):861-6.
Novel cytotoxic seco-abietane rearranged diterpenoids from Salvia prionitis.[Pubmed:
16206042]
METHODS AND RESULTS:
Six novel 4,5-seco-rearranged abietane diterpenoids, including one tetracyclic diterpenoid, prionoid A (1), two tricyclic diterpenoids, prionoid B (2) and prionoid C (3), and three dicyclic diterpenoids, Prionoid D (4), Prionoid E (5), and prionoid F (6), were isolated from the roots of Salvia prionitis Hance (Labiatae). Their structures were elucidated using spectroscopic analysis.
CONCLUSIONS:
The structure of 1 was further confirmed by a single-crystal X-ray diffraction determination. Moreover, it was found that 4 (IC50 = 0.41 microM) and 5 (IC50 = 0.72 microM) showed significant cytotoxic activity against P-388 and A-549 cell lines, respectively.
