On route II-c, two substances with a benzene ring structure similar to 4-hydroxyestrone were identified, and the peak area shows a decreasing trend, so inferred 3,4-dihydroxymandelic acid and catechol were the products of 4-hydroxyestrone cleavage, 4-hydroxyesrone had been reported as the product of E1 hydroxylation [ 6 , 40 ].
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<i>Lysinibacillus</i> sp. GG242 from Cattle Slurries Degrades 17β-Estradiol and Possible 2 Transformation Routes.
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