Synthesis of Idebenonyl Ester Prodrugs and Their Evaluation of Cancer Cells
<i>In Vitro</i>
作者:Song Mi Bae、Se Myeong Choi、Yeong‐seon Won、Kwon‐il Seo、Dai il Jung、Ju Hyun Song、Jong Hyun Cho
DOI:10.1002/bkcs.12246
日期:2021.4
Esterification of idebenone with commercially available straight‐chain aliphatic acids, branched‐chain aliphatic acids, aromatic acids, or nonsteroidal anti‐inflammatory drugs afforded their corresponding idebenonyl esters (5a–k) in good yield. The values of cell viability for RC‐58T cell at 50 μM were 86.3% for 5a, 75.9% for 5b, 23.4% for 5d, 61.2% for 5f, 67.9% for 5h, 70.6% for 5i, and 49.0% for
用市售的直链脂肪酸,支链脂肪酸,芳族酸或非甾体类抗炎药酯化艾地苯醌,可得到相应的艾地苯甲酸酯(5a – k),收率很高。对于RC-58T细胞的细胞活力的值在50μM分别为86.3%5a中,为75.9%5b中,为23.4%5d中,为61.2%5F,为67.9%5H,为70.6%5I,并为49.0%5J。