C-Furyl glycosides, I: Synthesis and antimicrobial evaluation of C-furyl glycosides and chalcones derived therefrom
摘要:
New C-furyl glycosides were synthesized in order to increase the number of compounds screened for antimicrobial activity. The antimicrobial activity showed that the bromo as well as the nitro derivatives were the most active compounds.
Synthesis of C-glycosylated cinnamoylfuran derivatives and their cytotoxic effects on cancer cells (MCF-7 and HeLa) and normal cells is presented.
合成C-糖基化肉桂酰呋喃衍生物及其对癌细胞(MCF-7和HeLa)和正常细胞的细胞毒作用被提出。
C-Furyl glycosides, I: Synthesis and antimicrobial evaluation of C-furyl glycosides and chalcones derived therefrom
作者:Wael A. El-Sayed、Mahmoud M. M. Ramiz、Adel A.-H. Abdel-Rahman
DOI:10.1007/s00706-008-0941-1
日期:2008.12
New C-furyl glycosides were synthesized in order to increase the number of compounds screened for antimicrobial activity. The antimicrobial activity showed that the bromo as well as the nitro derivatives were the most active compounds.