Drimiopsin D
Drimiopsin D is a natural product from Scilla scilloides.
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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.
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Nat Prod Bioprospect. 2015 October; 5(5): 263–270.
Lanostane-Type Triterpenoids from Scilla scilloides and Structure Revision of Drimiopsin D[Pubmed:
26458926]
METHODS AND RESULTS:
Two hitherto unknown lanostane-type triterpenoids, namely scillascillol (1) and scillascillone (2), and a hitherto unknown norlanostane-triterpene glycoside, namely scillascilloside B-1 (3), were isolated from the ethanol extract of the whole plants of Scilla scilloides.
CONCLUSIONS:
Their structures were elucidated on the basis of extensive spectroscopic studies. In addition, the structure of Drimiopsin D (6a) has been revised as 2,5-dimethoxy-8-methyl-1,3,6-trihydroxyxanthone (6) by reanalysis of the spectroscopic data.
J Nat Prod. 2004 Oct;67(10):1726-8.
Xanthones from Drimiopsis maculata.[Pubmed:
15497949 ]
METHODS AND RESULTS:
Six new xanthones, drimiopsin A, drimiopsin B, Drimiopsin C, Drimiopsin D, drimiopsin E, drimiopsin F , have been isolated from the South African Drimiopsis maculata.
CONCLUSIONS:
The structures of these compounds were difficult to elucidate due to the lack of correlating protons seen in the NMR spectra, and INADEQUATE spectra were used to confirm the structures. Xanthones have not previously been reported from the Hyacinthaceae.
