Podophyllol
Reference standards.
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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.
Arch Biochem Biophys.2020, 687:108384.
Microorganisms.2021, 9(12):2514.
Food Chem.2024, 436:137768.
Mie University2019, 10076.
Bull. Natl. Mus. Nat. Sci.2021, 47(2),109-114.
Pharm Biol.2022, 60(1):2040-2048.
Appl. Sci.2025, 15(1), 247
Development.2024, 151(20):dev202518.
Int J Mol Sci.2021, 22(10):5181.
J Control Release.2021, 336:159-168.
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J Pharm Sci. 1983 Oct;72(10):1158-61.
Antitumor agents LXII: Synthesis and biological evaluation of podophyllotoxin esters and related derivatives[Pubmed:
6644563 ]
METHODS AND RESULTS:
Synthetic esters of the C-4 hydroxyl group of podophyllotoxin (I) were prepared. In addition, esters were synthesized using the diol system of tetrahydropyranyl Podophyllol (XV), produced by reducing the lactone ring of tetrahydropyranyl podophyllotoxin with lithium aluminum hydride. Six compounds, the acrylate (IV), 3,3-dimethyl acrylate (V), phenoxyacetate (IX), and ethyl adipate (XI) of I as well as Podophyllol (XIV) and tetrahydropyranyl Podophyllol dimesylate (XVIII), showed significant activity when tested using the P-388 lymphocytic leukemia screen at 3 mg/kg/day.
CONCLUSIONS:
None of the esters showed higher activity than that shown by the parent molecule I when tested at the same dosage level.
