Cixiophiopogon A
Cixiophiopogon A is a natural product from Ophiopogon japonicus.
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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.
Curr Pharm Des.2024, 30(1):71-80.
Preprints2022, 2022030063.
J.of Traditional&Complementary Med.2022, 10.1016:j.jtcme.
The Journal of Supercritical Fluids2021, 176:105305.
Genes Genomics.2020, 10.1007
Molecules.2019, 24(7):E1290
Molecules.2022, 27(21):7643.
Foods.2020, 9(10):1348.
Antioxidants (Basel).2020, 9(4):284.
J Food Sci.2022, 87(11):4905-4916.
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Natural Product Research: Formerly Natural Product Letters Volume 25, Issue 1, 2011
A new steroidal glycoside from the Ophiopogon japonicus Ker-Gawler (Liliaceae)[Reference:
WebLink]
METHODS AND RESULTS:
A new steroidal glycoside (1), (25R)-14α, 17α-hydroxyspirost-5-en-3β-yl 3-O-α-L-rhamnpyranosyl-(1 → 2)-β-D-glucopyranosyl-(1 → 3)-β-D-glucopyranoside, together with three known steroidal glycosides, (25R)-3β-hydroxyspirost-5-en-1β-yl-3-O-α-L-rhamnopyranosyl-(1 → 2)-O-β-D-xylopyranosyl-(1 → 3)-α-L-arabinopyranoside (2), Cixi-ophiopogon B (3) and Cixiophiopogon A (4), were obtained from the tuberous roots of Ophiopogon japonicus (Liliaceae). Compound 2 was isolated from the Ophiopogon genus for the first time.
CONCLUSIONS:
Their structures were identified on the basis of extensive mass and nuclear magnetic resonance spectroscopic analysis.
