Sarracine N-oxide
Reference standards.
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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.
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Korean Journal of Pharmacognosy2019, 50(4):285-290
Int J Food Sci Nutr.2019, 70(7):825-833
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Bioorg Med Chem.2018, 26(14):4201-4208
Molecules.2018, 23(2)
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J.Food Processing & Preservation2022, jfpp.16666
Front Pharmacol.2023, 14:1095083.
Saudi Pharmaceutical Journal2023, 31(12):101829
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Magn Reson Chem. 2014 May;52(5):251-7.
Complete 1H NMR assignments of pyrrolizidine alkaloids and a new eudesmanoid from Senecio polypodioides.[Pubmed:
24574143]
METHODS AND RESULTS:
Chemical investigation of the aerial parts of Senecio polypodioides lead to the isolation of the new eudesmanoid 1β-angeloyloxyeudesm-7-ene-4β,9α-diol (1) and the known dirhamnosyl flavonoid lespidin (3), while from roots, the known 7β-angeloyloxy-1-methylene-8α-pyrrolizidine (5) and Sarracine N-oxide (6), as well as the new neoSarracine N-oxide (8), were obtained. The structure of 1 and 8 was elucidated by spectral means.
CONCLUSIONS:
Complete assignments of the (1)H NMR data for 5, 6, sarracine (7), and 8 were made using one-dimensional and two-dimensional NMR experiments and by application of the iterative full spin analysis of the PERCH NMR software.
