Revised Structures of Epohelmins A and B Isolated as Lanosterol Synthase Inhibitors from a Fungal Strain FKI-0929

Revised Structures of Epohelmins A and B Isolated as Lanosterol Synthase Inhibitors from a Fungal Strain FKI-0929
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DOI:
10.1038/ja.2005.82
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发表时间:
2005-09
期刊:
The Journal of Antibiotics
影响因子:
--
通讯作者:
M. Shibuya;B. Snider;Y. Sakano;H. Tomoda;S. Ōmura;Y. Ebizuka
M. Shibuya;B. Snider;Y. Sakano;H. Tomoda;S. Ōmura;Y. Ebizuka
中科院分区:
其他
文献类型:
--
作者:
M. Shibuya;B. Snider;Y. Sakano;H. Tomoda;S. Ōmura;Y. Ebizuka

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从真菌菌株FKI-0929中分离得到的毛甾醇合成酶抑制剂epohelmins A和B的结构分别为1α-羟基-3α-(4 ' -oxoundec-(5 ' E)-烯基)-吡咯利齐啶和1β-羟基-3α-(4 ' -oxoundec-(5 ' E)-烯基)-吡咯利齐啶。
The structures of epohelmins A and B isolated as lanosterol synthase inhibitors from a fungal strain FKI-0929 were revised to be 1α-hydroxy-3α-(4′-oxoundec-(5′ E)-enyl)-pyrrolizidine and 1β-hydroxy-3α-(4′-oxoundec-(5′ E)-enyl)-pyrrolizidine, respectively, by comparison with spectral data of synthetic compounds.