Design, total synthesis, and evaluation of novel open-chain epothilone analogues

被引:15
作者
Alhamadsheh, MM [1 ]
Hudson, RA
Tillekeratne, LMV
机构
[1] Univ Toledo, Coll Pharm, Dept Med & Biol Chem, Toledo, OH 43606 USA
[2] Univ Toledo, Coll Arts & Sci, Dept Chem, Toledo, OH 43606 USA
关键词
D O I
10.1021/ol0528787
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The design, total synthesis, and biological evaluation of two open-chain analogues of epothilone incorporating the critical C1-C8 fragment and the aromatic side chain held together by a small molecular scaffold have been achieved. Biological evaluation revealed that further restraint between the flexible C1-C8 region and the molecular scaffold may be necessary for potent inhibition of cell proliferation.
引用
收藏
页码:685 / 688
页数:4
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