Oximidines I and II:: Novel antitumor macrolides from Pseudomonas sp.

被引:104
作者
Kim, JW
Shin-ya, K
Furihata, K
Hayakawa, Y [1 ]
Seto, H
机构
[1] Univ Tokyo, Inst Mol & Cellular Biosci, Bunkyo Ku, Tokyo 1130032, Japan
[2] Univ Tokyo, Grad Sch Agr & Life Sci, Dept Appl Biol Chem, Bunkyo Ku, Tokyo 1138657, Japan
关键词
D O I
10.1021/jo9814997
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Our screening for cell-cycle inhibitors in transformed cells resulted in the isolation of novel active compounds, oximidines I (1) and II (2), from Pseudomonas sp. Q52002, The molecular formulas of 1 and 2 were established as C23H24N2O7 and C23H24N2O6, respectively, by high-resolution FABMS. The structures of the oximidines were elucidated by NMR spectral analysis, including a variety of two-dimensional techniques. The absolute stereochemistry of 1 was determined by using the modified Mosher method. The oximidines are novel 12-membered macrolides containing an O-methyloxime moiety. Oximidines I and II selectively inhibited the growth of rat 3Y1 cells transformed with E1A, ras, or src oncogenes.
引用
收藏
页码:153 / 155
页数:3
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