Isotussilagine
Reference standards.
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.
Saf Health Work.2019, 10(2):196-204
Phytother Res.2018, 32(5):923-932
J Chromatogr Sci.2020, 58(6):485-493.
J Funct Foods2019, 54:449-456
In Vitro Cellular & Developmental Biology - Plant 2021, 57:874¨C882.
J Med Food.2021, 24(2):151-160.
Phytochemistry.2021, 181:112539.
LWT2020, 124:109163
Cells.2022, 11(6):931.
Antibiotics (Basel).2024, 14(1):8.
Related and Featured Products
Planta Med. 1992 Dec;58(6):556-7.
Tussilagine and isotussilagine: two pyrrolizidine alkaloids in the genus arnica1.[Pubmed:
17226521]
METHODS AND RESULTS:
In flowerheads of ARNICA MONTANA, A. CHAMISSONIS ssp. FOLIOSA, A. AMPLEXICAULIS, and A. SACHALINENSIS, traces of the non-toxic pyrrolizidine alkaloids tussilagine and Isotussilagine were detected.
CONCLUSIONS:
Their identity was unambiguously confirmed by direct comparison (TLC, GC, GC/MS) with the authentic samples.
Tetrahedron Letters,1998,39(49): 9067–9068.
Enantioselective syntheses of tussilagine and isotussilagine[Reference:
WebLink]
METHODS AND RESULTS:
Tussilagine and Isotussilagine are synthesized through the coupling reactions of N,N-disubstituted β-amino-esters with methyl pyruvate and Mitsunobu reactions as key steps.
CONCLUSIONS:
The first enantioselective syntheses of tussilagine and Isotussilagine via the coupling reactions of N,N-disubstituted β-amino esters with methyl pyruvate are described.
