2. Neuronal Signaling
  3. Amyloid-β
  4. 42422-68-4

42422-68-4

Beta-Zearalanol Chemical Structure

42422-68-4

Chemical Structure

  • Beta-Zearalanol
  • CAS No: 42422-68-4
    Formula: C18H26O5
    Molecular Weight: 322.40
  • IUPAC Name: (3S,7S)-7,14,16-trihydroxy-3-methyl-3,4,5,6,7,8,9,10,11,12-decahydro-1H-benzo[c][1]oxacyclotetradecin-1-one
  • InChIKey: DWTTZBARDOXEAM-JSGCOSHPSA-N
  • SMILES: O=C1C2=C(O)C=C(O)C=C2CCCCC[C@H](O)CCC[C@H](C)O1

Biological Activity: Beta-Zearalenol is an mycotoxin produced by Fusarium spp, which causes apoptosis and oxidative stress in mammalian reproductive cells[1]. Beta-Zearalenol is the derivative of zearalenone (ZEA) which can conjugate with glucuronic acid[2].

Cat. No. Product Name Purity Description
HY-N6740R Beta-Zearalanol (Standard) ≥98% (±)-Nornicotine (Standard) is the analytical standard of (±)-Nornicotine. This product is intended for research and analytical applications. (±)-Nornicotine is the primary metabolite of nicotine that is formed through demethylation of nicotine in the genus Nicotiana tabacum L. (±)-Nornicotine is a precursor of tobacco-specific nitrosamine N-nitrosonornicotine. (±)-Nornicotine has detrimental effects to human health.
HY-N6740 Beta-Zearalanol 99.83% Beta-Zearalenol is an mycotoxin produced by Fusarium spp, which causes apoptosis and oxidative stress in mammalian reproductive cells. Beta-Zearalenol is the derivative of zearalenone (ZEA) which can conjugate with glucuronic acid.

References

[1]. Yang F, et al. Melatonin alleviates β-zearalenol and HT-2 toxin-induced apoptosis and oxidative stress in bovine ovarian granulosa cells. Environ Toxicol Pharmacol. 2019 May;68:52-60. [Content Brief]
[2]. Marin DE, et al. Cytotoxic and inflammatory effects of individual and combined exposure of HepG2 cells to zearalenone and its metabolites. Naunyn Schmiedebergs Arch Pharmacol. 2019 Aug;392(8):937-947. [Content Brief]

Keywords:

Beta-Zearalanol (Standard)Beta-Zearalanol