Acoforestinine

Acoforestinine
Product Name Acoforestinine
CAS No.: 110011-77-3
Catalog No.: CFN99502
Molecular Formula: C35H51NO10
Molecular Weight: 645.79 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: White powder
Source: The roots of Aconitum carmichaeli Debx.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price: $368/20mg
Acoforestinine is a natural product from Aconitum handelianum.
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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.
  • Int J Mol Sci.2021, 22(21):11836.
  • Heinrich Heine University Dusseldorf2021, 62203.
  • Biochem Pharmacol. 2020, 177:114014.
  • Natural Product Sciences2023, 29(4):276-280.
  • Comput Biol Med.2024, 178:108775.
  • J Appl Biol Chem.2024, 67:47,337-343.
  • Org Biomol Chem.2017, 15(31):6483-6492
  • Biochemistry.2018, 57(40):5886-5896
  • Mol Pharm.2018, 15(8):3285-3296
  • Phytomedicine Plus2022, 2(1):100207.
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    Zhongguo Zhong Yao Za Zhi. 2009 Aug;34(15):1927-9.
    Diterpenoid alkaloids from Aconitum handelianum.[Pubmed: 19894536]
    To investigate the alkaloids from Aconitum handelianum.
    METHODS AND RESULTS:
    The column chromatographic methods were employed for the isolation and purification of the chemical constituents. The structures were elucidated by spectroscopic methods. Eight diterpenoid alkaloids were isolated and identified as acoforine (1), Acoforestinine (2), 14-O-acetylsachaconitine (3), vilmorrianine C (4), vilmorrianine D (5), talatizamine (6), chasmanine (7) and yunaconitine (8).
    CONCLUSIONS:
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