Thirty novel 20 (S)-O-linked camptothecin (CPT) glycoconjugates were synthesized. They showed more potent in vitro cytotoxicities over irinotecan, but very weak direct topoisomerase I (Topo I) inhibition was observed at 100.0 μM. Oligosaccharide types, length of a PEG linker and acetyl groups exerted obvious effects on cytotoxicity, selectivity, water solubility and stability of the newly synthesized
合成了三十种新颖的20(S)-O-连接的
喜树碱(C
PT)糖缀合物。他们表现出更有效的体外细胞毒性过
伊立替康,但非常弱的直接拓扑异构酶I在100.0观察(TOPO I)抑制μ M.寡
糖类型,P
EG接头的长度和乙酰基作用于细胞毒性,选择性,
水溶性明显影响,并新合成的C
PT糖缀合物的稳定性。结构40与C
PT相比,
博来霉素(BLM)二糖与引入的酯部分中的
二甘醇相连,具有更高的抗肿瘤活性和独特的选择性。静脉内动物急性毒性(160 mg / kg)未检测到毒性。总的来说,将具有靶向肿瘤的
寡糖附着到C
PT的20(S)-OH上可以为当前的Topo I毒药带来的艰巨问题提供解决方案。