A series of activated iodo-benzamide derivatives are described as antineoplastic and antiviral drug compounds. The compounds generally possess a chelating group, a thiol trapping group and an activating group. The presumptive mechanism of action in preventing cancer cell and virus replication is through inhibition of the binding of transcription factors to zinc finger binding domains. The compounds are effective in inhibiting growth of a variety of human and animal tumor and leukemia cell lines at low concentrations.
一系列活化的
碘苯甲
酰胺衍
生物被描述为抗肿瘤和抗病毒药物化合物。这些化合物通常具有螯合基团,
硫醇捕捉基团和活化基团。预测的防止癌细胞和病毒复制的作用机制是通过抑制转录因子与
锌指结合域的结合。这些化合物在低浓度下有效抑制各种人类和动物肿瘤和白血病
细胞系的生长。