Structure-activity relationships of 1-(2-deoxy-2-fluoro-β-l-arabino-furanosyl) pyrimidine nucleosides as anti-hepatitis B virus agents
…, YL Zhu, JS Lin, K Shanmuganathan, J Du…
Index: Ma, Tianwei; Pai, S. Balakrishna; Zhu, Yong Lian; Lin, Ju Sheng; Shanmuganathan, Kirupa; Du, Jinfa; Wang, Chunguang; Kim, Hongbum; Newton, M. Gary; Cheng, Yung Chi; Chu, Chung K. Journal of Medicinal Chemistry, 1996 , vol. 39, # 14 p. 2835 - 2843
Full Text: HTML
Citation Number: 157
Abstract
Since 2'-fluoro-5-methyl-β-l-arabinofuranosyluracil (l-FMAU) has been shown to be a potent anti-HBV agent in vitro, it was of interest to study the structure-activity relationships of related nucleosides. Thus, a series of 1-(2-deoxy-2-fluoro-β-l-arabinofuranosyl) pyrimidine nucleosides have been synthesized and evaluated for antiviral activity against HBV in 2.2. 15 cells. For this study, l-ribose was initially used as the starting material. Due to the ...
Related Articles:
A practical synthesis of L-FMAU from L-arabinose
[Du, Jinfa; Choi, Yongseok; Lee, Kyeong; Chun, Byoung K.; Hong, Joon H.; Chu, Chung K. Nucleosides and Nucleotides, 1999 , vol. 18, # 2 p. 187 - 195]