Loeffler L J, Sajadi Z, Hall I H
J Med Chem. 1977 Dec;20(12):1578-84. doi: 10.1021/jm00222a008.
A series of N-protected vinyl, 1,2-dihaloethyl, and cyanomethyl esters of phenylalanine was synthesized and these compounds were evaluated for antitumor activity against the growth of Ehrlich ascites carcinoma in CF1 male mice (33 mg/kg/day), Walker 256 carcinosarcoma in Sprague-Dawley male rats (2.5 mg/kg/day), and P388 lymphocytic leukemia in DBA/2 mice (20 mg/kg/day). Structure-activity relationships were evaluated and acute toxicity studies (LD50 determinations) in male CF1 mice were also carried out on selected compounds. Carbobenzoxy-L0phenylalanine vinyl ester (5), N-carbobenzoxy-L-phenylalanine 1,2-dibromoethyl ester (12), and N-carbobenzoxy-L-phenylalanine cyanomethyl ester (8) were found to be very potent inhibitors of Ehrlich ascites tumor growth at nontoxic doses cited above. Compounds 5 and 12 also tripled survival time in the Walker 256 system. LD50 values for compounds 5, 12, and 8 were greater than 2000 mg/kg (greater than 6.15 mmol/kg), 74 mg/kg (0.15 mmol/kg), and 150 mg/kg (0.44 mmol/kg), respectively.
合成了一系列N-保护的苯丙氨酸乙烯酯、1,2-二卤代乙酯和氰甲基酯,并评估了这些化合物对CF1雄性小鼠(33毫克/千克/天)艾氏腹水癌生长、Sprague-Dawley雄性大鼠(2.5毫克/千克/天)Walker 256癌肉瘤以及DBA/2小鼠(20毫克/千克/天)P388淋巴细胞白血病的抗肿瘤活性。评估了构效关系,并对选定化合物在雄性CF1小鼠中进行了急性毒性研究(测定LD50)。发现苄氧羰基-L-苯丙氨酸乙烯酯(5)、N-苄氧羰基-L-苯丙氨酸1,2-二溴乙酯(12)和N-苄氧羰基-L-苯丙氨酸氰甲基酯(8)在上述无毒剂量下是艾氏腹水肿瘤生长的非常有效的抑制剂。化合物5和12在Walker 256系统中还使存活时间增加了两倍。化合物5、12和8的LD50值分别大于2000毫克/千克(大于6.15毫摩尔/千克)、74毫克/千克(0.15毫摩尔/千克)和150毫克/千克(0.44毫摩尔/千克)。