摘要：Incubation of 2-hydroxyestradiol (1) with rat liver homogenate in the presence of Sadenosyl-L-methionine and Mg2+ gave two isomeric monomethyl ethers, 2-methoxyestradiol (2) and 2-hydroxyestradiol-3-methyl ether (3). The ratio of the 2-O-methyl ether to the 3-O-methyl ether formed was found to be dependent on hydrogen ion concentration of the medium. At pH 6.0, the ratio was about 3-4, which decreased gradually with increasing pH, and at pH>7.0, the ratio was approaching to unity. PH dependency upon the product ratio was significant when 2, 3, 17β-trihydroxyestra-1, 3, 5 (10)-trien-6-one (5) was used as a substrate, although the ratio was completely reversed in contrast with the result obtained with 2-hydroxyestradiol. At pH 6-7, the ratio of the 3-O-methyl ether (7) to 2-O-methyl ether (6) was about 6-8. With increasing pH of the medium, 2-O-methylation increased gradually, and at over pH 8.0 the ratio became constant at about 3. These results suggest that rat liver catechol O-methyltransferase catalyzes the transfer of the methyl group from S-adenosyl-L-methionine to more basic hydroxyl group of the two phenolic hydroxyl groups of estrogen catechols.
关键词：transmethylation of 3, 4-dihydroxyacetophenone derivatives
