Adachi T, Tanaka A, Yamaha T
Division of Medical Chemistry, National Institute of Hygienic Sciences, Tokyo, Japan.
Radioisotopes. 1989 May;38(5):255-8. doi: 10.3769/radioisotopes.38.5_255.
Absorption, distribution, metabolism and excretion were studied in rats following a single oral administration of N-cyclohexyl-2-benzothiazyl sulfenamide (CBS) at a dose of 250 mg/kg. About 65% and 24% of the dose were excreted into urine and feces, respectively, for 3 days after administration of labeled CBS (cyclohexyl-14C). Biliary excretion amounted to about 5% of the dose for 3 days. While about 92% of the dose was recovered in urine and feces at a ratio of 1:1 within 3 days when 14C-2CBS was given. No specific organ-affinity was observed in distribution study. Cyclohexylamine and 2-mercaptobenzothiazole were identified as urinary metabolites.
在大鼠单次口服250mg/kg剂量的N-环己基-2-苯并噻唑次磺酰胺(CBS)后,对其吸收、分布、代谢和排泄情况进行了研究。给予标记的CBS(环己基-14C)后3天,约65%和24%的剂量分别经尿液和粪便排出。胆汁排泄量在3天内约占剂量的5%。给予14C-2CBS时,约92%的剂量在3天内以1:1的比例在尿液和粪便中回收。在分布研究中未观察到特定的器官亲和力。环己胺和2-巯基苯并噻唑被鉴定为尿液代谢物。