Isovallesiachotamine

Isovallesiachotamine
Product Name Isovallesiachotamine
CAS No.: 34384-71-9
Catalog No.: CFN92641
Molecular Formula: C21H22N2O3
Molecular Weight: 350.4 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: The seeds of Strychnos nux-vomica Linn.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Standard reference
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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.
  • Jour. of Stored Pro & Postharvest Res.2016, 7(3):32-36
  • Aging (Albany NY).2021, 13(19):22867-22882.
  • Srinagarind Medical Journal2017, 32(1)
  • J Clin Transl Hepatol.2023, 11(4):863-876.
  • Evid Based Complement Alternat Med.2021, 2021:8707280.
  • Spectrochim Acta A2019, 210:372-380
  • Molecules.2021, 26(19):6032.
  • Preprints2021, doi:10.20944
  • Life (Basel).2021, 11(12):1399.
  • Sci Rep. 2018, 10590
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    Planta Med. 1982 May;45(5):28-30.
    Vallesiachotamine and isovallesiachotamine from the seeds of Strychnos tricalysioides.[Pubmed: 17396774]

    METHODS AND RESULTS:
    A new indole alkaloid, 11-hydroxypolyneuridine, was isolated from Vinca major subsp. major L. and the known indole alkaloids vallesiachotamine and Isovallesiachotamine from Vinca minor L. This is the first report on the alkaloids of both Vinca species growing in Turkey; vallesiachotamine and Isovallesiachotamine were isolated from a Vinca species for the first time. V. minor may be considered as a new source for these two alkaloids due to their occurrence in high amount in the aerial parts of the plant.
    CONCLUSIONS:
    The alkaloid extracts of the two Vinca species were found to have high lipid peroxidation inhibitory and DPPH radical scavenging activities. Anticholinesterase activity of the extracts was also very strong.
    J Nat Prod. 2003 Jul;66(7):1017-21.
    Turbinatine, a potential key intermediate in the biosynthesis of corynanthean-type indole alkaloids.[Pubmed: 12880329]

    METHODS AND RESULTS:
    Extraction of the leaves of Chimarrhis turbinata has led to the isolation of turbinatine (1), a new corynanthean-type indole alkaloid, besides four known indole alkaloids, strictosidine, 5alpha-carboxystrictosidine, vallesiachotamine, and Isovallesiachotamine. The structural determination of 1 was based on 1D and 2D spectroscopic data.
    CONCLUSIONS:
    An evaluation of the DNA-damaging activities of the isolates was performed by means of a bioassay using mutant strains of Saccharomyces cerevisiae, which indicated these compounds were weakly active.
    Nat Prod Commun. 2012 Jun;7(6):731-4.
    Indole alkaloids from Vinca major and V. minor growing in Turkey.[Pubmed: 22816294]

    METHODS AND RESULTS:
    Extraction of the leaves of Chimarrhis turbinata has led to the isolation of turbinatine (1), a new corynanthean-type indole alkaloid, besides four known indole alkaloids, strictosidine, 5alpha-carboxystrictosidine, vallesiachotamine, and Isovallesiachotamine. The structural determination of 1 was based on 1D and 2D spectroscopic data.
    CONCLUSIONS:
    An evaluation of the DNA-damaging activities of the isolates was performed by means of a bioassay using mutant strains of Saccharomyces cerevisiae, which indicated these compounds were weakly active.
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