2. Natural Products
  3. Disease Research Fields Plants Flavonoids Phenols
  4. Other Diseases Elaeagnaceae Flavonols Polyphenols
  5. Hippophaë rhamnoides
  6. 2202-01-9

2202-01-9

Eichlerialactone Chemical Structure

2202-01-9

Chemical Structure

  • Eichlerialactone
  • CAS No: 2202-01-9
    Formula: C27H42O4
    Molecular Weight: 430.62
  • IUPAC Name: 3-((3S,3aR,5aR,6S,7S,9aR,9bR)-6,9a,9b-trimethyl-3-((S)-2-methyl-5-oxotetrahydrofuran-2-yl)-7-(prop-1-en-2-yl)dodecahydro-1H-cyclopenta[a]naphthalen-6-yl)propanoic acid
  • InChIKey: LEKUPXHLKIIVCR-FAKJQIDCSA-N
  • SMILES: C[C@]12[C@]3([C@@](CC[C@]1([H])[C@]([C@]4(OC(CC4)=O)C)([H])CC2)([H])[C@](C)([C@H](C(C)=C)CC3)CCC(O)=O)C

Biological Activity: Eichlerialactone is a sesquiterpene compound isolated from Chisocheton penduliflorus. Eichlerialactone is weakly cytotoxic to breast cancer cells[1].

Cat. No. Product Name Purity Description
HY-W016412 Coenzyme Q0 99.88% Coenzyme Q0 (CoQ0) is a potent, oral active ubiquinone compound can be derived from Antrodia cinnamomea. Coenzyme Q0 induces apoptosis and autophagy, suppresses of HER-2/AKT/mTOR signaling to potentiate the apoptosis and autophagy mechanisms. Coenzyme Q0 regulates NFκB/AP-1 activation and enhances Nrf2 stabilization in attenuation of inflammation and redox imbalance. Coenzyme Q0 has anti-angiogenic activity through downregulation of MMP-9/NF-κB and upregulation of HO-1 signaling.

References

[1]. Jarinporn Phongmaykin, et al. A new sesquiterpene and other terpenoid constituents of Chisocheton penduliflorus. Arch Pharm Res. 2008 Jan;31(1):21-7. [Content Brief]

Keywords:

Eichlerialactone