Vellosimine
Standard reference
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.
Sci Rep. 2018, 462(8)
Environ Toxicol.2019, 34(4):513-520.
Cell Physiol Biochem.2017, 44(4):1381-1395
J-STAGE2015, 249-255
University of Burgos2024, ssrn.4795441.
Expert Opin Ther Targets.2024, :1-11.
J Food Sci Technol.2019, 56(5):2712-2720
Sains Malaysiana2024, 53(2):397-408.
Nat Prod Sci.2016, 22(2)
J Agric Food Chem.2024, 72(40):22237-22249.
Related and Featured Products
Org Lett. 2000 Jul 13;2(14):2057-9.
General approach for the synthesis of sarpagine/ajmaline indole alkaloids. Stereospecific total synthesis of the sarpagine alkaloid (+)-vellosimine.[Pubmed:
10891229]
METHODS AND RESULTS:
(+)-Vellosimine has been synthesized enantiospecifically in 27% overall yield from commercially available D-(+)-tryptophan methyl ester via the asymmetric Pictet-Spengler reaction and a stereocontrolled intramolecular palladium-coupling reaction as key steps.
Angew Chem Int Ed Engl. 2015 Jan 2;54(1):315-7.
Enantioselective, protecting-group-free total synthesis of sarpagine alkaloids--a generalized approach.[Pubmed:
25346454]
METHODS AND RESULTS:
A generalized synthetic access to sarpagine alkaloids through a joint synthetic sequence has been accomplished. Its applicability is showcased by the enantioselective total syntheses of Vellosimine (1), N-methylVellosimine (3), and 10-methoxyVellosimine (8).
