Three new, 1-oxygenated ent-8,9-secokaurane diterpenes from Croton kongensis

被引:15
作者
Chen, W
Yang, XD
Zhao, JF
Yang, JH
Zhang, HB
Li, ZY [1 ]
Li, L
机构
[1] Kunming Univ Sci & Technol, Sch Environm Sci & Engn, Kunming 650093, Yunnan, Peoples R China
[2] Yunnan Univ, Res Sch Pharm, Minist Educ, Key Lab Med Chem Nat Resource, Kunming 650091, Peoples R China
关键词
D O I
10.1002/hlca.200690057
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Three new ent-8,9-secokaurane diterpenes, kongensins A-C (1-3), were isolated from the aerial parts of Croton kongensis, together with two known compounds, rabdoumbrosanin (4) and (7 alpha,14 beta)-7,14-dihydroxy-ent-kaur-16-en-15-one (5). The structures of the new compounds were elucidated by HR-MS as well as in-depth 1D- and 2D-NMR analyses. Compounds 1-3 showed an unusual oxygenation pattern, with an AcO or OH group at C(1), in combination with a Delta(8(14)) unsaturation (1) or an 8,14-epoxide function (2, 3).
引用
收藏
页码:537 / 541
页数:5
相关论文
共 7 条
[1]   Cytotoxic 7,20-epoxy ent-kauranoids from Isodon xerophilus [J].
Hou, AJ ;
Zhao, QS ;
Li, ML ;
Jiang, B ;
Lin, ZW ;
Sun, HD ;
Zhou, YP ;
Lu, Y ;
Zheng, QT .
PHYTOCHEMISTRY, 2001, 58 (01) :179-183
[2]  
Institute of Botany Chinese Academy of Science, 1996, FLOR REIP SIN, V44, P123
[3]  
*JINGS NEW MED I, 1977, DICT CHIN TRAD HERB, P507
[4]  
NODE M, 1985, CHEM PHARM BULL, V33, P1029
[5]   11-oxygenated cytotoxic 8,9-secokauranes from a New Zealand liverwort, Lepidolaena taylorii [J].
Perry, NB ;
Burgess, EJ ;
Baek, SH ;
Weavers, RT ;
Geis, W ;
Mauer, AB .
PHYTOCHEMISTRY, 1999, 50 (03) :423-433
[6]  
TAKEDA Y, 1983, PHYTOCHEMISTRY, V22, P2531, DOI 10.1016/0031-9422(83)80156-3
[7]   New antimycobacterial and antimalarial 8,9-secokaurane diterpenes from Croton kongensis [J].
Thongtan, J ;
Kittakoop, P ;
Ruangrungsi, N ;
Saenboonrueng, J ;
Thebtaranonth, Y .
JOURNAL OF NATURAL PRODUCTS, 2003, 66 (06) :868-870