Abiesadine I

Abiesadine I
Product Name Abiesadine I
CAS No.: 1210347-50-4
Catalog No.: CFN99330
Molecular Formula: C24H34O5
Molecular Weight: 402.5 g/mol
Purity: >=98%
Type of Compound: Diterpenoids
Physical Desc.: Powder
Source: The herbs of Pinus yunnanensis
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.
  • Int J Mol Sci.2022, 23(23):14826.
  • Sci Rep.2020, 10:4495(2020)
  • Front Pharmacol.2021, 12:761922.
  • Int J Mol Sci.2021, 22(21):11836.
  • PLoS One.2022, 17(6):e0268505.
  • Research Square2022, rs.3.rs-1948239
  • Pharmacognosy Journal, 2021, 13(5).
  • Biol Pharm Bull.2018, 41(11):1645-1651
  • J Agric Food Chem.2020, 68(43):12164-12172.
  • Sci Rep.2019, 9(1):4342
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    METHODS AND RESULTS:
    Twenty-five new (abiesadines A–Y, Abiesadine I, 1–25, ) and 29 known (26–54) diterpenes were isolated from the aerial parts of Abies georgei. Abiesadine A (1) is a novel 8,14-seco-abietane, while abiesadine B (2) is a novel 9,10-seco-abietane. The structures of the new compounds were established on the basis of spectroscopic data analysis. Manool (52) showed the strongest effect against LPS-induced NO production in RAW264.7 macrophages with the IC50 value of 11.0 μg/mL. In another anti-inflammatory assay against TNFα-triggered NF-κB activity, (12R,13R)-8,12-epoxy-14-labden-13-ol (54) exhibited the strongest effect (IC50 = 8.7 μg/mL).
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