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2-叔丁基苯并噻唑衍生物对成年卡里尼丝虫的体外抗丝虫效果

Antifilarial efficacy in vitro of 2-tert-butyl-benzothiazole derivatives on adult Litomosoides carinii.

作者信息

Zahner H, Franz M, Köhler P, Striebel H P

机构信息

Institut für Parasitologie Justus-Liebig-Universität, Giessen Fed. Rep. of Germany.

出版信息

Arzneimittelforschung. 1991 Aug;41(8):821-7.

PMID:1781804
Abstract

Six 2-tert-butyl-benzothiazole derivatives (2-tert-butyl-6-isothiocyanato-5-methyl-benzothiazole (CGP 21306); 3-[(2-tert-butyl-5-methyl-benzothiazole-6-yl)aminothiocar-bonyl thiol] propionic acid (CGP 21835); 2-tert-butyl-5-methyl-6-(N-methyl-piperazinyl-thiocarbonylamino)- benzothiazole(CGP 21833); 2-tert-butyl-5-methyl-6-(4-dimethylamino-piperid-1-yl-thiocarbo nylamino)- benzothiazole (CGP 26702); CGP 20376, the 5-methoxy analogue to CGP 21835 and CGP 20309, the 5-methoxy analogue to CGP 21833) were tested in vitro against adult Litomosoides carinii. When exposed to the drugs in protein-free medium RPMI 1640 drug concentrations of 1 nmol/ml caused complete immobilization of female worms within 4 h (CGP 21306, 21835, 20376) or 20 h (CGP 21833, 26702, 20309). Short term exposure for 1 h had similar effects with CGP 21306, 21835, 21833 and 20376. However, the levels of CGP 26702 and 20309 (both thiourea derivatives) had to be increased to 10 nmol/ml to obtain complete immobilization after short term exposure. Male parasites were more resistant to the drugs than females under these experimental conditions. When the medium was supplemented with 10% foetal calf serum (FCS) the efficacy of all compounds was reduced. The effect of the compounds during permanent and short term exposure on the release of microfilariae was determined over an incubation period of 7 days (medium RPMI 1640/10% FCS). In general only drug concentrations which affected markedly the motility of the worms within 2 days reduced significantly the number of microfilariae released by treated worms.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对六种2-叔丁基-苯并噻唑衍生物(2-叔丁基-6-异硫氰酸根合-5-甲基-苯并噻唑(CGP 21306);3-[(2-叔丁基-5-甲基-苯并噻唑-6-基)氨基硫代羰基硫醇]丙酸(CGP 21835);2-叔丁基-5-甲基-6-(N-甲基-哌嗪基-硫代羰基氨基)-苯并噻唑(CGP 21833);2-叔丁基-5-甲基-6-(4-二甲基氨基-哌啶-1-基-硫代羰基氨基)-苯并噻唑(CGP 26702);CGP 20376,CGP 21835的5-甲氧基类似物以及CGP 20309,CGP 21833的5-甲氧基类似物)进行了体外抗成年卡里尼丝虫的测试。当在无蛋白培养基RPMI 1640中接触这些药物时,1 nmol/ml的药物浓度可使雌虫在4小时内(CGP 21306、21835、20376)或20小时内(CGP 21833、26702、20309)完全固定。用CGP 21306、21835、21833和20376进行1小时的短期接触有类似效果。然而,CGP 26702和20309(两种硫脲衍生物)的浓度必须提高到10 nmol/ml才能在短期接触后实现完全固定。在这些实验条件下,雄性寄生虫比雌性对药物更具抗性。当培养基中添加10%胎牛血清(FCS)时,所有化合物的效力都会降低。在7天的孵育期(培养基RPMI 1640/10% FCS)内测定了这些化合物在长期和短期接触期间对微丝蚴释放的影响。一般来说,只有在2天内显著影响虫体运动的药物浓度才会显著减少经处理虫体释放的微丝蚴数量。(摘要截断于250字)

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