New indolopyridoquinazoline, benzo[c]phenanthridines and cytotoxic constituents from Zanthoxylum integrifoliolum

被引:68
作者
Chen, JJ [1 ]
Fang, HY
Duh, CY
Chen, IS
机构
[1] Tajen Inst Technol, Dept Pharm, Grad Inst Pharmaceut Technol, Pingtung 907, Taiwan
[2] Natl Sun Yat Sen Univ, Inst Marine Resources, Kaohsiung 80424, Taiwan
[3] Kaohsiung Med Univ, Sch Pharm, Kaohsiung, Taiwan
关键词
Zanthoxylum integrifoliolum; Rutaceae; root bark; 7,8-dehydro-1-methoxyrutaecarpine; isodecarine; 8-demethyloxychelerythrine; cytotoxicity;
D O I
10.1055/s-2005-864144
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Three new alkaloids, 7,8-dehydro-1-methoxyrutaecarpine, isodecarine, and 8-demethyloxychelerythrine, together with sixteen known compounds, norchelerythrine, oxychelerythrine, decarine, dihydrochetythrinylacetaldehyde, 6-acetonyldihydro-chelerythrine, rutaecarpine, 1-hydroxyrutaecarpine, gamma-fagarine, skimmianine, (-)-matairesinol, (-)-isoarctigenin, (+)-epipinoresinol, d-sesamin, lupeol, canthin-6-one, and arnottianamide have been isolated from the root bark of Zanthoxyluin integrifoliolum. The structures of these new compounds were determined through spectral analyses. Among the isolates, 7,8-dehydro-1 -methoxyrutaecarpine, norchelerythrine, oxychelerythrine, dihydrocherythrinylacetaldehyde, 6-acetonyldihydrochelerythrine, 1-hydroxyrutaecarpine, gamma-fagarine, skimmianine, (-)-matairesinol, and canthin-6-one exhibited cytotoxicities (ED50 values < 4 yg/mL) against P-388 or HT-29 cell lines in vitro.
引用
收藏
页码:470 / 475
页数:6
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