Antiarol
Antiarol is a member of aromatic phenols and exhibits moderate DPPH free radical scavenging activity.
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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.
Plants (Basel).2021, 10(7):1376.
Biomedicine & Pharmacotherapy2022, 153:113404.
Russian Journal of Bioorganic Chemistry2023, 49:1689¨C1698.
Appl. Sci. 2021, 11(8),3437.
BMC Plant Biol.2022, 22(1):128.
Korean J. of Horticultural Sci. & Tech. 2017, 793-804
Front Pharmacol.2022, 13:919230.
Nutrients.2023, 15(6):1417.
Antioxidants (Basel).2021, 10(9):1435.
Phytother Res.2015, 29(7):1088-96
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Australian Journal of Chemistry, 1973 , 26 (11) :2459
A revision of the structures proposed for the melicope extractives, melicopol and methylmelicopol[Reference:
WebLink]
2, 4, 6-Trihydroxybenzoic acid was converted by partial methylation, formylation, and then reduction into methyl 2-hydroxy-3-hydroxymethyl-4, 6-dimethoxybenzoate (5) which proved different from dimethyldegeranylmelicopol. Methyl 6-geranyloxy-2-hydroxy-3-hydroxymethyl-4-methoxybenzoate (4), its neryl analogue (7), and methyl 4-geranyloxy-2-hydroxy-3-hydroxymethyl-6-methoxybenzoate (21) were prepared similarly but all were different from methylmelicopol. From a re-investigation of earlier work, melicopol and methylmelicopol were assigned new structures, 6'-geranyloxy-2, 2', 4'-tri-hydroxy-3'-methoxyacetophenone (31) and its 4'-methyl ether derivative (24), respectively. Dimethyldegeranylmelicopol, 2, 6'-dihydroxy-2', 3', 4'-trimethoxyacetophenone (25), was prepared from Antiarol (28) and acetoxyacetonitrile.
