1,3-Diacetylvilasinin
1,3-Diacetylvilasinin shows marginal cytotoxicities against certain human tumor cell lines. It also shows antifeeding activity towards insects.
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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.
Korean Herb. Med. Inf.2021, 9(2):231-239.
J Ethnopharmacol.2016, 194:219-227
Int J Mol Sci.2022, 23(13):7115.
Int Immunopharmacol.2021, 101(Pt A):108181.
Green Chem.2023, 25:5222-5232
Molecules.2020, 25(3):734
J Holistic Integrative Pharm.2023, 4(1):14-28
VNU J Science: Med.&Pharm. Sci.2023, 39(2):43-52.
Pharm Biol.2021, 59(1):134-145.
J Nat Med.2021, doi: 10.1007.
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J Nat Prod. 1998 Jan;61(1):64-70.
New bioactive triterpenoids from Melia volkensii.[Pubmed:
9461654]
METHODS AND RESULTS:
Bioactivity-directed fractionation of the root bark of Melia volkensii resulted in the isolation of two new natural products, meliavolkinin (1) and melianin C (3), together with two known compounds, 1,3-Diacetylvilasinin (2) and melianin B (4). Jones oxidation of 4 gave compounds 3, 23,24-diketomelianin B (5), and 16,23,24-triketomelianin B (6). The structures of the new compounds were elucidated by spectral and chemical data.
CONCLUSIONS:
Compounds 1-6 all showed marginal cytotoxicities against certain human tumor cell lines, while 5 showed selective cytotoxicities for the human prostate (PC-3) and pancreatic (PACA-2) cell lines with potencies comparable to those of adriamycin.
