Ifflaiamine
Ifflaiamine is a natural product from Flindersia ifflaiana F. Muell.
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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 Issues Mol Biol.2023, ;45(2):1601-1612.
Mol Med Rep.2023 Oct;28(4):193.
Naunyn Schmiedebergs Arch Pharmacol.2024, 03148-x.
Nat Commun.2024, 15(1):8221.
Front Pharmacol.2018, 9:236
Pharmaceuticals (Basel). 2021, 14(10):986.
Biomed Pharmacother.2020, 131:110673.
Molecules.2019, 24(22):E4022
J Mol Med (Berl).2018, 96(7):661-672
Nutr Cancer.2023, 75(1):376-387.
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Australian Journal of Chemistry, 1963, 16(2):737-743.
The Chemical Constituents of Australian Flindersia Species. XVII. The Structure of Ifflaiamine[Reference:
WebLink]
The wood of Flindersia ifflaiana F. Muell. contains ifflaionic acid, a new triterpene acid, and Ifflaiamine, a new alkaloid. The latter has a modified furoquinoline structure, shown to be (I). Some experiments on the synthesis of 4-hydroxy-2-quinolone and derivatives are described.
