Sutherlandin trans-p-coumarate
Sutherlandin trans-p-coumarate is a naturally rare cyanogenic glycoside.
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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.
Food Res Int.2019, 123:125-134
Research Square2021, 10.21203.
Appl. Sci.2022, 12(17), 8646.
Biomed Pharmacother.2022, 145:112474.
Acta Physiologiae Plantarum2015, 37:1736
Biochem Biophys Res Commun.2020, 522(4):1052-1058
Front Pharmacol.2021, 12:765521.
Toxicol Res.2019, 35(4):371-387
Heliyon.2023, e12778.
Metabolites.2023, 13(6):689.
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Zhongguo Zhong Yao Za Zhi. 2011 May;36(9):1198-201.
Chemical constituents from Exochorda racemosa.[Pubmed:
21842649]
To study the chemical constituents of Exochorda racemosa.
METHODS AND RESULTS:
Compounds were isolated and purified by silica gel, Sephadex LH-20, MCI gel and RP-18 column chromatography, and their structures were determined by spectroscopic analysis.
Twenty compounds were isolated and identified as N-p-coumaroyl-N'-caffeoylputrescine (1), Sutherlandin trans-p-coumarate (2), apigenin 7-O-methylglucuronide (3), astragalin (4), nicotiflorin (5), kaempferol 3-neohesperidoside (6), rutin (7), apigenin (8), luteolin (9), linalool-1-oic acid (10), betulalbuside A (11), ursolic acid (12) , corosolic acid (13), gynuramide II (14), beta-sitosterol (15), daucosterol (16), uridine (17), adenosine (18), syringin (19), and trans4-hydroxycinnamic acid (20), respectively.
CONCLUSIONS:
All compounds were obtained from this plant for the first time, moreover, 1 was reported as a new natural product, and 2 is a naturally rare cyanogenic glycoside.
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