Sulfocostunolide A
Reference standards.
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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.
China Pharmacy2015, 26(27)
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Phytomedicine.2022, 99:154025.
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Microb Pathog.2019, 131:128-134
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Plant Pathology2022, 13527
Molecules.2021, 26(4):816.
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Zhongguo Zhong Yao Za Zhi. 2012 May;37(9):1249-53.
Chemical constituents of Dolomiaea souliei.[Pubmed:
22803370]
To study the chemical constituents of Dolomiaea souliei.
METHODS AND RESULTS:
Various chromatographic techniques were adopted to separate the constituents, and the spectrum analysis was made to identify their structures.
Seventeen compounds were isolated and identified as: dehydrocostus lactone (1), costunolide (2), mokko lactone (3), santamarine(4), reynosin (5), 4alpha-hydroxy-4beta-methyldihydrocostol (6), Sulfocostunolide A (7), beta-costic acid (8), beta-cyclocostunolide (9), vladinol A (10), ursolic acid (11), betulinic acid (12), betulin (13), dibutyl terephthalate (14), dibutyl phthalate (15), uridine (16), and emodin (17).
CONCLUSIONS:
Compounds 6-9 and 12-17 were obtained from this genus for the first time, and compound 11 was obtained from this plant for the first time.
Chem Pharm Bull (Tokyo). 2008 Jun;56(6):864-5.
Sulfonated guaianolides from Saussurea lappa.[Pubmed:
18520098]
METHODS AND RESULTS:
Two new guaiane-type sesquiterpene lactones with an unusual sulfonic acid group, Sulfocostunolide A (1) and sulfocostunolide B (2), were isolated from the roots of Saussurea lappa.
Their structures were elucidated on the basis of extensive spectroscopic analysis.
