,Synthesis and anti-tumor activity of alkenyl camptothecin esters

• 作 者: Zhi-song CAO John MENDOZA Albert DEJESUS Beppino GIOVANELLA
• 机 构: Stehlin Foundation for Cancer Research and St Joseph Hospital Cancer Laboratory,1918 Chenevert Stree
• 出 处: 中国药理学报（英文版）
• 发表日期: 2005年2期
• 关键词: alkaloids camptothecin 9-nitrocamptothecin structure-activity relationship

Aim: To study the degrees of influence of changing side ester chains at position C20 of camptothecin on the anti-tumor activity of the molecules. Methods: The esterification reaction of camptothecin 1 and 9-nitrocamptothecin 2 with crotonic anhydride in pyridine gave the corresponding esters 3 and 4, respectively. The acylation of 1 and 2 with cinnamoyl chloride gave products 7 and 8. Epoxidation reaction of 3 and 4 with m-chloroperoxybenzoic acid in benzene solvent gave the products 5 and 6. Esters 3, 4, and 5 were tested for anti-tumor activity against 14 human cancer cell lines. Results: Both in vitro and in vivo anti-tumor activity studies for these esters were conducted and the data demonstrated positive results, that is, these esters were active against the tested tumor lines. Conclusion: Alkenyl esters 3 and 4 showed strong anti-tumor activity in vitro against 14 different cancer cell lines. Ester 3 was active against human breast carcinoma in mice and the toxicity of the agent was not observed in mice during the treatment, implying that this agent is effective for treatment with low toxicity.