ent-kaurane diterpenoids from the leaves of Isodon xerophilus

被引:19
作者
Li, SH
Niu, XM
Peng, LY
Zhang, HJ
Yao, P
Sun, HD [1 ]
机构
[1] Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources W China, Kunming 650204, Peoples R China
[2] Univ Illinois, Coll Pharm, Program Collaborat Res Pharmaceut Sci, Chicago, IL USA
关键词
D O I
10.1055/s-2002-34926
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
From the ethanolic extract of the leaves of Isodon xerophilus, three new ent-kaurane diterpenoids named xerophilusins L-N (1-3), together with three known ones designated as rabdoternin A (4), longikaurin F (5) and ponicidin (6), were isolated and structurally elucidated. Compound 6 demonstrated most potent cytotoxic activity against K562 and T24 human tumor cell lines with IC50 = 0.09 and 0.32 mug/ml, respectively.
引用
收藏
页码:946 / 948
页数:3
相关论文
共 10 条
[1]   TERPENOIDS .27. STRUCTURE AND STEREOCHEMISTRY OF PONICIDIN, A DITERPENOID OF ISODON-JAPONICUS [J].
FUJITA, E ;
TAOKA, M ;
SHIBUYA, M ;
FUJITA, T ;
SHINGU, T .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1973, (20) :2277-2281
[2]   LONGIKAURIN-C, LONGIKAURIN-D, LONGIKAURIN-E AND LONGIKAURIN-F - NEW ANTI-BACTERIAL DITERPENOIDS FROM RABDOSIA-LONGITUBA [J].
FUJITA, T ;
TAKEDA, Y ;
SHINGU, T .
HETEROCYCLES, 1981, 16 (02) :227-230
[3]   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
[4]  
Hou AJ, 2001, CHINESE J CHEM, V19, P365
[5]   New 7,20:14,20-diepoxy ent-kauranoids from Isodon xerophilus [J].
Hou, AJ ;
Li, ML ;
Jiang, B ;
Lin, ZW ;
Ji, SY ;
Zhou, YP ;
Sun, HD .
JOURNAL OF NATURAL PRODUCTS, 2000, 63 (05) :599-601
[6]   Cytotoxic ent-kaurane diterpenoids from Isodon eriocalyx var. laxiflora [J].
Niu, XM ;
Li, SH ;
Li, ML ;
Zhao, QS ;
Mei, SX ;
Na, Z ;
Wang, SJ ;
Lin, ZW ;
Sun, HD .
PLANTA MEDICA, 2002, 68 (06) :528-533
[7]   Crystal structure of a 1:1 complex of natural diterpenoids: Absolute configurations and unambiguous NMR spectral assignments of neoangustifolin and epinodosinol [J].
Sun, HD ;
Qiu, SX ;
Lin, LZ ;
Zhang, RP ;
Zhou, YS ;
Zheng, QT ;
Johnson, ME ;
Fong, HHS ;
Farnsworth, NR ;
Cordell, GA .
JOURNAL OF NATURAL PRODUCTS, 1997, 60 (03) :203-206
[8]   Crystal and molecular structures of a natural equimolecular mixture of two epimeric diterpenes [J].
Sun, HD ;
Qiu, SX ;
Lobkovsky, EB ;
Lin, LZ ;
Farnsworth, NR ;
Clardy, J ;
Fong, HHS .
TETRAHEDRON, 2001, 57 (01) :65-70
[9]  
SUN HD, 2001, DITERPENOIDS ISODON, pP5
[10]   STUDIES ON THE DITERPENOID CONSTITUENTS OF RABDOSIA-TERNIFOLIA - STRUCTURAL ELUCIDATION OF NEW DITERPENOIDS, RABDOTERNIN-A, RABDOTERNIN-B AND RABDOTERNIN-C [J].
TAKEDA, Y ;
TAKEDA, K ;
FUJITA, T ;
SUN, HD ;
MINAMI, Y .
CHEMICAL & PHARMACEUTICAL BULLETIN, 1990, 38 (02) :439-442