Acetylanonamine

Acetylanonamine
Product Name Acetylanonamine
CAS No.: 138079-62-6
Catalog No.: CFN00428
Molecular Formula: C21H29NO8
Molecular Weight: 423.46 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: The herbs of Senecio scandens
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
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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  • Journal of Natural Remedies2024, 24(3):555¨C575.
  • Cell Signal.2022, 99:110433.
  • Bioengineering2023, 10(10), 1113.
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  • bioRxiv - Biochemistry2023, 548213.
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  • J. of Med. Plant Research.2013, 90-151
  • Molecules.2021, 26(4):816.
  • Int J Biol Macromol.2020, 161:1230-1239.
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    J Nat Prod. 1991 Sep-Oct;54(5):1425-6.
    Acetylanonamine, a new secopyrrolizidine alkaloid from Senecio anonymus.[Pubmed: 1800641]

    METHODS AND RESULTS:
    A new secopyrrolizidine alkaloid, Acetylanonamine, was isolated from Senecio anonymus. The structure was established by high resolution nmr (1H-1H COSY and 1H-13C HETCOR), ms, comparison of these spectral data with those of anonamine, and synthesis of 1 from 2.
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