Lanceolarin
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.
Universidade Estadual Paulista2017, 42785
Front Plant Sci.2024, 15:1458916.
Food Funct.2020, 11(2):1322-1333.
Separations2021, 8(6),80.
J Physiol Biochem.2024, 80(2):421-437.
Comparative Clinical Pathology 2021, 30:961-971.
J Sep Sci.2018, 41(7):1682-1690
Pol J Microbiol.2021, 70(1):117-130.
Front Microbiol.2024, 15:1429027.
J Anal Toxicol.2021, bkab015.
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Zhongguo Zhong Yao Za Zhi. 2009 Aug;34(15):1921-6.
Constituents of Millettia nitida var. hirsutissima.[Pubmed:
19894535]
To separate effective constituents from Millettia nitida var. hirsutissima.
METHODS AND RESULTS:
Compounds were isolated by chromatography methods, structures were identified by spectroscopic means.
Eight flavonoids (1-8) and two triterpenes (9-10) were isolated from this plant. They were identified as calycosin (1), genistin (2), gliricidin (3), 8-O-methylretusin (4), afromosin-7-O-beta-D-glucopyranoside (5), Lanceolarin (6), soliquiritigenin (7), symplocoside (8), lupeol (9), 3beta-friedelanol (10).
CONCLUSIONS:
The compounds (1-10) were obtained from M. nitida var. hirsutissima for the first time. The 13C-NMR dada of 1 were correct assignment on the basis of 2D-NMR spectral analysis.
