Isoleojaponin

Isoleojaponin
Product Name Isoleojaponin
CAS No.: 1840966-49-5
Catalog No.: CFN89151
Molecular Formula: C20H26O3
Molecular Weight: 314.42 g/mol
Purity: >=98%
Type of Compound: Diterpenoids
Physical Desc.: Oil
Source: The herbs of Leonurus japonicus.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Isoleojaponin is a natural product from Leonurus japonicus.
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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 J. Medicinal Crop Sci.2023, 31(5):283-289.
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    Molecules. 2015 Jan 7;20(1):839-45.
    Isoleojaponin, a new Halimane diterpene isolated from Leonurus japonicus.[Pubmed: 25574824 ]

    METHODS AND RESULTS:
    Leojaponin (2), a labdane diterpene, was isolated from the EtOH extract of the herb of Leonurus japonicus together with a new halimane diterpene named Isoleojaponin (1).
    CONCLUSIONS:
    Isoleojaponin has a new diterpene skeleton with a unique cross-conjugated α,β-unsaturated ketone system, Their structures were elucidated by physical and spectroscopic analysis, and the relative configuration of the chiral C-9 carbon was determined by a computational method, and analysis of its possible biogenesis pathways.
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