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)。