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作 者:陈海英[1] 潘启超[1] 郑懿雅 王沛滋 余小强[2] 陈永向
机构地区:[1]中山医科大学肿瘤研究所,广州510060 [2]中山大学化学系,广州510275
出 处:《癌症》1990年第3期209-212,共4页Chinese Journal of Cancer
摘 要:我们研究了19种有生物活性载体(磺胺、9-氨吖啶、对氨水杨酸及异烟肼)的植物生长抑制剂(4氯或2,4—双氯或2,4,5一三氯苯氧乙酸,2,3,5一三氯苯甲酸或α—蔡乙酸)衍生物在体外对低分化鼻咽癌细胞株CNE_2生长的抑制作用。属于含二或三氯的苯氧乙酸与磺胺类或9—氨吖啶的结合物,在100μg/ml浓度下,对细胞生长的抑制率>50%者有9种药物,>80%者有5种,其IC_(50)已测定,效力最强的2,4一二氯苯氧乙酰9—氨基吖啶(2,4—D—ACD的IC_(50)为4.58μg/ml,有进一步作体内抗癌作用研究的价值。The growth inhibitory action of 19 derivatives of plant growth regulators ( 4- choro or 2,4- dichloro- or 2,4,5- trichloro-phenyloxoacetic acid ; 2,3,5- trichloroben-zoic acid ; α - naphthyla cetic acid ) with biological active carriers ( sulfonamides, 9 - aminoacridine, p-aminosalicylic acid, isoniazide ) on poorly differentiated nasopharyngeal carcinoma cell line CNE 2 was studied. At the concentration of 100 μg/ml 9 compounds showed cell growth inhidition rate>50%, 5 compounds >80%. They are the derivatives of di-or tri-choloro-phenyloxoacetic acid with sulfonamides or 9 -aminoacridine. Their IC 50's have been determined. The most potent one is 2,4 - dichloro-phenyloxoacetyl-amino-ac-ridine with an IC50 of 4.58 μg/ml. It is worth while to further study its in vivo antitumor activity.
分 类 号:R730.231.3[医药卫生—肿瘤]
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