Conjugates (A1–A5) of the Pt(iv) derivative (A6) with amino groups from peracetyl glucose, rhamnose and mannose with a propyl amino or ethyl amino linker at the reducing end were synthesized and exhibited significant therapeutic efficacy in tumour cells, especially for prostate cancer (PCa).
使用从过乙酰葡萄糖、鼠李糖和甘露糖的氨基团合成的铂(IV)衍生物(A6)的共轭物(A1-A5),在还原端具有丙基氨基或乙基氨基连接剂,表现出显著的治疗效果对于肿瘤细胞,尤其是前列腺癌(PCa)。