p-Hydroxyphenethyl anisate
p-Hydroxyphenethyl anisate is a natural product from Notopterygium incisum.
Inquire / Order:
manager@chemfaces.com
Technical Inquiries:
service@chemfaces.com
Tel:
+86-27-84237783
Fax:
+86-27-84254680
Address:
1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
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.
Acta Physiologiae Plantarum2016, 38:7
Foods.2022, 11(12):1708.
J Cell Mol Med.2023, 27(11):1592-1602.
J Ethnopharmacol.2016, 194:219-227
Dicle Tip Dergisi2020, 47(2),423-430.
Mol Med Rep.2022, 25(1):8.
Food Chem.2021, 360:130063.
Curr Issues Mol Biol.2023, 45(2):1587-1600.
Current Enzyme Inhibition2023, 19(1):55-64(10)
Front Pharmacol.2019, 10:1025
Related and Featured Products
Zhongguo Zhong Yao Za Zhi. 2008 Dec;33(24):2918-21.
Studies on chemical constituents in roots and rhizomes of Notopterygium incisum.[Pubmed:
19294850]
To study the chemical constituents in the roots and rhizomes of Notopterygium incisum.
METHODS AND RESULTS:
The chemical constituents were isolated by various column chromatographic methods and structurally elucidated by NMR and MS evidences. Twenty-four compounds were obtained and identified as isocalamenediol (1), pregnenolone (2), beta-sitosterol (3), bergapten (4), bergaptol (5), cnidilin (6), isoimperatorin (7), bergamottin (8), demethylfuropinnarin (9), nodakenetin (10), 7'-O-methylnotoptol (11), notopterol (12), notoptol (13), pabulenol (14), phenethylferulate (15), p-Hydroxyphenethyl anisate (16), trans-ferulic acid (17), nodakenin (18), sucrose (19), 2-methoxy-4-(3-methoxy-1-propenyl)-phenol (20), 3, 4, 5 trimethoxy-trans-cinnamic acid (21), p-methoxycinnamic acid (22), 4-acetoxy-3-methoxy-trans-cinnamic acid (23), and p-hydroxy-trans-cinnamic acid (24).
