Ifflaiamine
Ifflaiamine is a natural product from Flindersia ifflaiana F. Muell.
Inquire / Order:
manager@chemfaces.com
Technical Inquiries:
service@chemfaces.com
Tel:
+86-27-84237783
Fax:
+86-27-84254680
Address:
1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
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.
Org Biomol Chem.2017, 15(31):6483-6492
Nat Commun.2023, 14(1):5075.
Int Immunopharmacol.2019, 71:361-371
Univerzita Karlova2022, 173245.
Molecules.2019, 25(1):E103
Chulalongkorn University2024, ssrn.4716057.
Drug Chem Toxicol.2024,1-12.
Ulm University Medical Center2020, doi: 10.18725.
Front Pharmacol.2022, 13:806869.
Appl. Sci. 2021, 11(22),10569
Related and Featured Products
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.
