Sitsirikine
Sitsirikine is a natural product from Catharanthus roseus.
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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.
Comput Biol Chem.2019, 83:107096
Foods.2022, 11(6):882.
J Agric Food Chem.2023, 71(47):18510-18523.
Polytechnic University of Catalonia2017, 105826
Pharmacognosy Magazine2018, 14(56):418-424
Int J Mol Sci.2022, 23(24):16000.
Clin Exp Pharmacol Physiol.2020, doi: 10.1111
Univerzita Karlova2022, 228192.
Environ Toxicol.2023, 38(5):1174-1184.
Environ Toxicol.2024, 39(4):2417-2428.
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Helvetica Chimica Acta, 2015 , 98 (10) :1381-6.
A Novel Alkaloid from Aspidosperma pyricollum (Apocynaceae) and Complete 1 H and 13 C Chemical Shift Assignments[Reference:
WebLink]
METHODS AND RESULTS:
A novel natural product indole, alkaloid, named rel-pyricolluminol (1), was isolated from Aspidosperma pyricollum Müll.Arg. together with six known metabolites Sitsirikine (2), aparicin (3), ulein (4), stemmadenine (5), lupeol (6), and (3β)-sitoster-3-yl β-D-glucopyranoside (7).
CONCLUSIONS:
These compounds were characterized on the basis of their spectral data, mainly 1D- (1H,13C-DEPTQ) and 2D-NMR (1H,1H-COSY, NOESY, HSQC, and HMBC), and mass spectra (EI-MS and HR-ES-MS), involving also comparison with data from the literature.
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