PNU 157977:一种新型强效抗肿瘤药物,对注射L1210白血病细胞的小鼠具有低体内毒性。

Anti-cancer drug design Pub Date : 1999-02-01
P G Baraldi, G Balboni, R Romagnoli, G Spalluto, P Cozzi, C Geroni, N Mongelli, C Rutigliano, N Bianchi, R Gambari
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引用次数: 0

摘要

本文介绍了2的二溴氮芥衍生物PNU 157977的设计、合成、体外和体内抗L1210小鼠白血病的活性,并讨论了其构效关系。这种二溴衍生物的细胞毒性几乎比具有相同寡肽链的二氯衍生物高两个数量级(IC50为2.7 ng/ml对225 ng/ml),并且在体内的生存时间比他莫司汀和2 (T/C 750对133和213)分别长5倍和3倍。此外,PNU 157977对M5076实体瘤的活性明显低于相近的2。以雌激素受体PCR探针作为足迹靶分子的足迹实验表明,PNU 157977与2或他莫司汀相比具有不同的序列特异性烷基化和更强的裂解活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
PNU 157977: a new potent antitumour agent exhibiting low in vivo toxicity in mice injected with L1210 leukaemia cells.

The design, synthesis, in vitro and in vivo activity against L1210 murine leukaemia of the dibromo nitrogen mustard derivative of 2, called PNU 157977, is described and the structure-activity relationship discussed. This dibromo derivative is almost two orders of magnitude more cytotoxic than the dichloro counterpart having the same oligopeptidic chain (IC50 2.7 ng/ml versus 225 ng/ml), and it showed in vivo an increased survival time which is 5- and 3-fold longer than that of tallimustine and 2 (and T/C 750 versus 133 and 213) respectively. Moreover PNU 157977 shows activity against the M5076 solid tumour markedly inferior to that of the closely analogous 2. Footprinting experiments conducted using the oestrogen receptor PCR probe as the footprinting target molecule show that PNU 157977 possesses a different sequence-specific alkylation and greater cleavage activity than either 2 or tallimustine.

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