Bakke J E, Feil V J, Price C E
J Environ Sci Health B. 1976;11(3):225-30. doi: 10.1080/03601237609372038.
Rats metabolized single oral doses of O,O-diethyl-O(3,5,6-trichloro-2-pyridyl-2,6-14C) phosphorothioate to at least six radiolabeled urinary metabolites. The urine contained about 90 percent of the dose. Three of these metabolites were identified as the glucuronide of 3,5,6-trichloro-2-pyridinol (80% the urinary 14C), a glycoside of 3,5,6-trichloro-2-pyridinol (4%), and 3,5,6-trichloro-2-pyridinol (12%).
大鼠口服单剂量的O,O-二乙基-O(3,5,6-三氯-2-吡啶基-2,6-¹⁴C)硫代磷酸酯后,可将其代谢为至少六种放射性标记的尿液代谢物。尿液中含有约90%的给药剂量。其中三种代谢物被鉴定为3,5,6-三氯-2-吡啶醇的葡糖醛酸苷(占尿液¹⁴C的80%)、3,5,6-三氯-2-吡啶醇的糖苷(4%)和3,5,6-三氯-2-吡啶醇(12%)。