1beta,10beta-Epoxydesacetoxymatricarin

1beta,10beta-Epoxydesacetoxymatricarin
Product Name 1beta,10beta-Epoxydesacetoxymatricarin
CAS No.: 124020-39-9
Catalog No.: CFN89005
Molecular Formula: C15H18O4
Molecular Weight: 262.30 g/mol
Purity: >=98%
Type of Compound: Sesquiterpenoids
Physical Desc.: Powder
Targets: HMG-CoA Reductase | TNF-α | MMP(e.g.TIMP)
Source: The herbs of Achillea wilhelmsii.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
1beta,10beta-Epoxydesacetoxymatricarin shows high anti-hypercholesterolemic potential.
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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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  • Asian Journal of Chemistry2014, 26(22):7811-7816
  • J Mater Chem B.2019, 7(39):5896-5919
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  • Journal of Apicultural Research2021, 60(1)
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    This study was done to identify the content compounds of Achillea wilhelmsii (A. wilhelmsii) and to evaluate its hypoglycemic and anti-hypercholesterolemic activity and effect on inflammatory mediators.
    METHODS AND RESULTS:
    The extracts and fractions of A. wilhelmsii were thoroughly analyzed using high performance liquid chromatography (HPLC), and the total content of phenols and flavonoids was determined. The hypoglycemic activity was evaluated in vivo using alloxan-induced diabetic mice. The effect upon inflammatory mediators was evaluated in vitro using the human monocytic leukemia cell line (THP-1). The anti-hypercholesterolemic activity was evaluated in vitro using the 3-hydroxy-3-methylglutaryl-CoA (HMG-CoA) reductase assay kit. The water extract (WE)-treated group showed the highest reduction in the fasting blood glucose levels (FBGL). The chloroform fraction (CF) and ethyl acetate fraction (EAF) both showed a significant ability to reduce the secretion of tumor necrosis factor alpha (TNF-α). The EAF, however, also attenuated the levels of matrix metalloproteinase-2 (MMP-2) and matrix metalloproteinase-9 (MMP-9). The CF showed the most significant 3-hydroxy-3-methylglutaryl-CoA reductase (HMGR) inhibition activity. The five main compounds in the CF were isolated and identified.
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    Out of the five compounds in the CF,1beta,10beta-Epoxydesacetoxymatricarin (CP1) and leucodin (CP2) showed the highest anti-hypercholesterolemic potential. A molecular docking study provided corresponding results.
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    METHODS AND RESULTS:
    The electronic circular dichroism (CD) spectrum of the sesquiterpenoid 1beta,10beta-Epoxydesacetoxymatricarin (1) measured in the microcrystalline solid state differs from the solution one in the appearance of a pronounced vibrational fine structure in the long-wavelength region (n-π* enone transition) and of a new moderately intense band in the π-π* region. TDDFT CD calculations were run on input structures derived from the X-ray geometry of 1 to reproduce the impact of exciton-type couplings between proximate molecules in the crystals.
    CONCLUSIONS:
    The vibrational structure of the CD spectrum was also reproduced for the isolated molecule by modelling the potential energy surfaces at the harmonic level and taking into account Duschinsky and Herzberg-Teller effects.
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