20835-90-9
Chemical Structure
β-Epoxysitosterol
- CAS No.: 20835-90-9
- Formula:C29H50O2
- Molecular Weight:430.72
IUPAC Name: (3S,4aS,5aR,6aS,6bS,9R,9aR,11aS,11bR)-9-((2R,5R)-5-ethyl-6-methylheptan-2-yl)-9a,11b-dimethylhexadecahydrocyclopenta[1,2]phenanthro[8a,9-b]oxiren-3-ol
InChIKey: ZBNPKSZFWFSSQK-FVKRCMCYSA-N
SMILES: C[C@]12[C@]3([C@](O3)(C[C@@]4([C@@]1(CC[C@@]5(C)[C@]4(CC[C@@]5([C@@H](CC[C@H](C(C)C)CC)C)[H])[H])[H])[H])[H])C[C@@H](O)CC2
Biological Activity: β-Epoxysitosterol is an Estrogen receptor α agonist. β-Epoxysitosterol accumulates in the plasma, aorta, liver, kidney and heart of hamsters fed with diets containing phytosterol oxidation products. β-Epoxysitosterol can be used in the research of liver cancer[1][2].
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β-Epoxysitosterol | β-Epoxysitosterol is an Estrogen receptor α agonist. β-Epoxysitosterol accumulates in the plasma, aorta, liver, kidney and heart of hamsters fed with diets containing phytosterol oxidation products. β-Epoxysitosterol can be used in the research of liver cancer. | |||||||||||||||||||||
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- [1]. Ryan E, et al. Phytosterol oxidation products: their formation, occurrence, and biological effects[J]. Food Reviews International, 2009, 25(2): 157-174.
- [2]. Takayasu BS, et al. Biological effects of an oxyphytosterol generated by β-Sitosterol ozonization. Archives of biochemistry and biophysics. 2020 Dec 15;696:108654.
Keywords
