Yonemoto J, Brown N A, Webb M
Toxicol Lett. 1984 Apr;21(1):97-102. doi: 10.1016/0378-4274(84)90229-7.
The secondary metabolite of dimethoxyethyl phthalate (DMEP), methoxyacetic acid (MAA), but neither the diester nor either of its primary metabolites, monomethoxyethyl phthalate (MMEP) and 2-methoxyethanol (ME), interferes with normal growth and development of organogenesis phase rat embryos in culture. These in vitro observations suggest that the teratogenicity of DMEP in vivo is due to enzymic cleavage of the diester to ME, followed by oxidation of the latter to MAA in the maternal compartment.
邻苯二甲酸二甲氧基乙酯(DMEP)的次生代谢产物甲氧基乙酸(MAA),而非该二酯及其两种主要代谢产物单甲氧基乙基邻苯二甲酸酯(MMEP)和2-甲氧基乙醇(ME)中的任何一种,会干扰培养中处于器官发生期的大鼠胚胎的正常生长和发育。这些体外观察结果表明,DMEP在体内的致畸性是由于该二酯在母体部分被酶解为ME,随后ME被氧化为MAA所致。