Lochnericine

Lochnericine
Product Name Lochnericine
CAS No.: 72058-36-7
Catalog No.: CFN97697
Molecular Formula: C21H24N2O3
Molecular Weight: 352.43 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: The herbs of Catharanthus roseus (L.)G.Don
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Lochnericine (LOC) is a component of Voacanga africana, which is a type of traditional medical food in Africa widely used for treating diseases.
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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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    Luminescence. 2015 Mar;30(2):240-6.
    Spectroscopy and docking simulations of the interaction between lochnericine and bovine serum albumin.[Pubmed: 24942935]
    Lochnericine (LOC) is a component of Voacanga africana, which is a type of traditional medical food in Africa widely used for treating diseases.
    METHODS AND RESULTS:
    In this article, the interaction between Lochnericine and bovine serum albumin (BSA) was studied by fluorescence spectroscopy. Furthermore, Fourier transform infrared (FTIR), Raman and circular dichroism (CD) were used to investigate the structural changes of BSA. The experimental results consistently indicated that Lochnericine changed the secondary structure of BSA. Three structure-similar components were used to study the interference experiments.
    CONCLUSIONS:
    The molecular modeling results showed that Lochnericine could bind within not only sites I and II, but also bind the cavity of subdomain IB.
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