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Autor:
Fardos N. M. Naguib, Mahmoud H. el Kouni, Zhi Hao Chen, Edward Chu, Zum Yao Weng, Ming Y. Chu, Sungman Cha, Elizabeth C. Rowe, Shih Hsi Chu
Publikováno v:
Nucleosides and Nucleotides. 7:91-102
Furanosyl analogs of BAU (5-benzylacyclouridine) and BBAU (5-benzyloxybenzylacyclouridine), two potent inhibitors of uridine phosphorylase, were synthesized and evaluated as potential cancer chemotherapeutic agents. The analogs included ribosides, 2,