体内
脚印
体外
L1210细胞
化学
细胞毒性T细胞
立体化学
IC50型
劈理(地质)
药理学
烷基化
细胞毒性
分子生物学
生物化学
生物
DNA
断裂(地质)
基序列
催化作用
古生物学
生物技术
作者
Baraldi Pg,Gianfranco Balboni,Romeo Romagnoli,Giampiero Spalluto,Pier Giorgio Cozzi,Cristina Geroni,Nicola Mongelli,Cristina Rutigliano,Nicoletta Bianchi,Roberto Gambari
出处
期刊:PubMed
日期:1999-02-01
卷期号:14 (1): 71-6
被引量:5
摘要
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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