Ajugacumbin 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.
Molecules 2021, 26(4),1092.
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Evid Based Complement Alternat Med.2021, 8707280.
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Molecules.2021, 26(13):4081.
Heliyon2022, 8(2):e08866.
Foods.2022, 11(12):1708.
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Chinese Chemical Letters, 1996, 7(5):411-414.
Selective reduction of clerodane diterpenoids.[Reference:
WebLink]
METHODS AND RESULTS:
The α, β-unsaturated γ-lactones of neo-clerodane diterpenoids teucvidin, teupernin E and Ajugacumbin A were selectively transformed into saturated Y -lactones and unsaturated diol derivatives with NaBE4.
These transformations are of interest due to their selective reduction as compared with catalytic hydrogenation and LiAlH4 reduction of these diterpenoid compounds.
