(-)-Isodocarpin

(-)-Isodocarpin
Product Name (-)-Isodocarpin
CAS No.: 10391-08-9
Catalog No.: CFN92313
Molecular Formula: C20H26O5
Molecular Weight: 346.4 g/mol
Purity: >=98%
Type of Compound: Diterpenoids
Physical Desc.: Powder
Source: The herbs of Isodon japonicus
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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  • J Cell Physiol.2021, 236(3):1950-1966.
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  • Natural Product Communications2023, 18(9).
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  • Int J Mol Sci.2019, 20(8):E1855
  • (-)-Isodocarpin

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    Angewandte Chemie International Edition.
    Divergent Total Syntheses of Enmein-Type Natural Products:(-)-Enmein, (-)-Isodocarpin and (-)-Sculponin R.[Reference: WebLink]

    METHODS AND RESULTS:
    Divergent total syntheses of enmein-type natural products, (–)-enmein, (-)-Isodocarpin and (–)-sculponin R, have been achieved in a concise fashion.
    CONCLUSIONS:
    Key features of the strategy include (a) an efficient early-stage cage formation to control succeeding diastereoselectivity, (b) an one-pot acylation/akylation/lactonization to construct the C-ring and C8 quarternary center, (c) a reductive alkenylation approach to construct enmain D/E rings and (d) a flexible route to allow divergent syntheses of three natural products.
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