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Synthesis and antitumor activity of novel pyrimidinyl pyrazole derivatives. III. Synthesis and antitumor activity of 3-phenylpiperazinyl-1-trans-propenes

机译:新型嘧啶基吡唑衍生物的合成及抗肿瘤活性。三, 3-苯基哌嗪基-1-反式丙烯的合成及抗肿瘤活性

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摘要

A series of novel 3-[4-phenyl-1-piperazinyl]-1-15-methyl-1-(2-pyrimidinyl)-4-pyrazolyl]-1-trans-propenes and related compounds were synthesized and evaluated by their cytotoxic activity against several tumor cell lines in vitro and in vivo antitumor activity against some tumor models when administered both intraperitoneally and orally. Compounds with the 3-chloropyridin-2-yl group (9g) and the 3-fluoro-5-substituted phenylpiperazinyl group (29b, c, and e) showed significantly potent cytotoxicity by in vitro testing. Among them, the 3-cyano-5-fluorophenyl derivative (29b) exhibited potent antitumor activity against several tumor cells including human carcinoma without causing undesirable effects in mice.
机译:合成了一系列新型的3- [4-苯基-1-哌嗪基] -1-15-甲基-1-(2-嘧啶基)-4-吡唑基] -1-反式丙烯及其相关化合物,并对其细胞毒性进行了评价。当腹膜内和口服给药时,其对几种肿瘤细胞系的体外和体内抗肿瘤活性对某些肿瘤模型具有抗性。通过体外测试,具有3-氯吡啶-2-基(9g)和3-氟-5-取代苯基哌嗪基(29b,c和e)的化合物显示出显着的有效细胞毒性。其中,3-氰基-5-氟苯基衍生物(29b)对包括人癌在内的几种肿瘤细胞表现出有效的抗肿瘤活性,而不会对小鼠造成不良影响。

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