LePage G A, Khaliq A
Cancer Treat Rep. 1979 Jan;63(1):53-7.
alpha-2'-Deoxythioguanosine (alpha-TGdR) was administered as a single dose to 13 cancer patients in 18 experiments at dose levels of 150--1500 mg/m2 and as a daily dose to 22 patients in 42 experiments at dose levels of 100--4000 mg/m2/day X 5 days. No significant toxicity was observed. Blood levels and rates of excretion were determined with radiosulfur-labeled alpha-TGdR. Approximately 80% of the dose was excreted in the urine in 24 hours, initially as unchanged alpha-TGdR and increasingly as metabolites. Metabolites appear to be nucleosides and do not include 6-thioguanine, 6-thioxanthine, or 6-thiouric acid to any measurable extent. Small amounts of the alpha-TGdR in blood samples were bound to albumin and to erythrocyte membranes. Blood plasma levels of alpha-TGdR at the highest doses were in the range of 200--300 micrometer, declining in 24 hours to 67--124 micrometer.
α-2'-脱氧硫代鸟苷(α-TGdR)在18项实验中以150 - 1500毫克/平方米的剂量水平单剂量给予13名癌症患者,并在42项实验中以100 - 4000毫克/平方米/天×5天的剂量水平每日给药22名患者。未观察到明显毒性。用放射性硫标记的α-TGdR测定血药浓度和排泄率。约80%的剂量在24小时内从尿液中排出,最初以未改变的α-TGdR形式排出,随后代谢产物排出量逐渐增加。代谢产物似乎是核苷,在任何可测量的程度上均不包括6-硫鸟嘌呤、6-硫黄嘌呤或6-硫尿酸。血样中的少量α-TGdR与白蛋白和红细胞膜结合。最高剂量下α-TGdR的血浆水平在200 - 300微摩尔范围内,24小时内降至67 - 124微摩尔。