https://www.selleckchem.com/products/AC-220.html
Two photochemically generated oligomers were found to contribute to estrogenic activity, produced from the cleavage of excited triplet state molecules and subsequent radical-radical reactions. Computational toxicology results showed that the increased estrogenic activity was attributed to oligomer [4-Hydroxy-isophthalic acid 1-ethyl ester 3-(4-hydroxy-phenyl)] and its EC50 was lower than that of the parent EP. In contrast, OH-adducts exhibited higher EC50 values than the parent EP, while still possessing estrogenic activity. Therefore, m
Like
Comment
Share
