Erythrinin A
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.
J Cell Mol Med.2018, 22(9):4236-4242
Faculty of Chem. & Nat. Resource Eng.2014, 62
Biomed Pharmacother.2024, 173:116319.
Phytother Res.2019, 33(4):1104-1113
Mol Biol Rep.2024, 51(1):117.
J Ethnopharmacol.2017, 196:75-83
Journal of Ginseng Research2019, 10.1016
Plants (Basel).2024, 13(6):868.
Food Control2022, 132:108434.
Academic J of Second Military Medical University2019, 40(1)
Related and Featured Products
Other References Information
Tetrahedron, 1985,41 (12) :2479-2482.
Synthesis of erythrinin A, a naturally occurring pyranoisoflavone[Reference:
WebLink]
Erythrinin A ( 10) has been synthesised by the oxidative rearrangement of dihydropyranochalcone 1 with thallium(III) nitrate (TTN) in trimethyl orthoformate (TMOF) to the dimethyl acetal 2, followed by cyclisation to 3, demethylation to 6 and dehydrogenation. Compound 10 could also be obtained from chalcone 4 on similar rearrangement followed by cyclisation, demethoxymethylation and dehydrogenation. In another route, chalcone 7 was oxidatively rearranged with TTN in TMOF, to 8 which on treatment with HCl yielded 10.
