Maneekarn Namsa-AidSuthep WiyakruttaSurasak PrachyaAnucha Namsa-AidApichart SuksamrarnChulabhorn Research InstituteRamkhamhaeng UniversityMahidol UniversitySrinakharinwirot University2022-08-042022-08-042021-11-01Trends in Sciences. Vol.18, No.21 (2021)277402262-s2.0-85121593308https://repository.li.mahidol.ac.th/handle/20.500.14594/79286The macrolide brefeldin A (BFA, 1) exhibited high cytotoxicity against KB cells. However, it was also toxic against non-cancerous cells. In order to lower toxicity against normal cells while maintaining the cytotoxic potency to the cancer cells, structural modification of this compound was undertaken. Starting from compound 1, the analogues 2-13 were synthesized and evaluated for cytotoxicity against KB cells. The analogue 2 exhibited the most potent cytotoxicity against KB cells, with an IC50 value of 0.034 nM, 67-fold more active than its parent compound 1. It was 41764 and 8235 fold more active than the standard drugs ellipticine and doxorubicin, respectively. The higher cytotoxicity against KB cells and lower toxicity against Vero cells of analogue 2 than those of the parent compound 1 contributed to its exceptionally high selectivity index of 9117. The results suggested that this analogue might be utilized to develop a new candidate for an anticancer drug.Mahidol UniversityMultidisciplinaryArticleSCOPUS10.48048/tis.2021.44