Blepharotriol
Blepharotriol may have antimicrobial and cytotoxic activities.
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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.
Pharmaceuticals (Basel).2024, 17(10):1368.
Korean Herb. Med. Inf.2020, 8(2):233-242.
Indian J Pharm Sci.2022, 84(4): 874-882.
Plant Physiol Biochem.2023, 202:107913.
Molecules.2022, 27(7):2116.
J. Mater. Life Sci.2024, 3:2:78-87
Antioxidants (Basel).2023, 12(1):189.
Int J Mol Sci.2020, 21(6):2190.
Int J Mol Sci.2024, 25(15):8101.
Plant Direct.2021, 5(4):e00318.
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Tetrahedron, 2005, 61(9):2513-2519.
New phenolic triterpenes from Maytenus blepharodes. Semisynthesis of 6-deoxoblepharodol from pristimerin[Reference:
WebLink]
METHODS AND RESULTS:
Four new phenolic triterpenes with a 24-nor-D:A-friedoleane skeleton, isoblepharodol, 7-oxoblepharodol, Blepharotriol and 6-deoxoblepharodol, were isolated from Maytenus blepharodes.
Their structures were elucidated on the basis of spectroscopic analysis, including homo and heteronuclear correlation NMR experiments (COSY, ROESY, HSQC, and HMBC). The semisynthesis of 6-deoxoblepharodol and its epimer at C-8 was achieved by catalytic reduction of pristimerin, a quinone-methide triterpene present in the plant. The biosynthetic formation of the phenolic triterpenes isolated from this species is also discussed.
CONCLUSIONS:
The compounds were assayed for antimicrobial and cytotoxic activities.
