Chinensine B

Chinensine B
Product Name Chinensine B
CAS No.: 849245-34-7
Catalog No.: CFN97409
Molecular Formula: C20H28O3
Molecular Weight: 316.4 g/mol
Purity: >=98%
Type of Compound: Diterpenoids
Physical Desc.: Powder
Source: The rhizomes of Alpinia chinensis
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Chinensine B and Chinensines A, C, D and Ε are antitumor diterpenoids.
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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.
  • Acta Pharm Sin B.2015, 5(4):323-9.
  • Plants (Basel).2023, 12(22):3877.
  • Sci Rep.2018, 8(1)
  • J.Food Processing & Preservation2022, jfpp.16666
  • Front Pharmacol.2020, 11:566490.
  • Front. Pharmacol.2022, 901563.
  • Toxicol In Vitro.2018, 52:94-105
  • University of Limpopo2016, 1777
  • Int J Mol Sci.2022, 23(13):7115.
  • Processes2021, 9(1), 153.
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    METHODS AND RESULTS:
    In this dissertation the successful syntheses of natural products that exhibit interesting biological activities are described. In particular, the first total synthesis of the antitumor diterpenoids Chinensine B (3) and Chinensines A, C, D and Ε (2, 4-6) is disclosed herein. En route to the Chinensines, Coronarin E (1), as well as natural products 65, 79 and Villosin (92) were synthesized.
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