Intercedensides A-C, three new cytotoxic triterpene glycosides from the sea cucumber Mensamaria intercedens Lampert

被引:90
作者
Zou, ZR
Yi, YH
Wu, HM
Wu, JH
Liaw, CC
Lee, KH
机构
[1] Second Mil Med Univ, Sch Pharm, Res Ctr Marine Drugs, Shanghai 200433, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Bioorgan & Nat Prod Chem, Shanghai 200032, Peoples R China
[3] Dept Pharm, Beijing 100101, Peoples R China
[4] Univ N Carolina, Sch Pharm, Nat Prod Lab, Chapel Hill, NC 27599 USA
来源
JOURNAL OF NATURAL PRODUCTS | 2003年 / 66卷 / 08期
关键词
D O I
10.1021/np030064y
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Three new triterpene glycosides, intercedensides A (1), B (2), and C (3), were isolated from the sea cucumber Mensamria intercedens Lampert, which is found in the South China Sea, and their structures have been elucidated by spectroscopic analysis (NMR and ESIMS) and chemical transformations. Intercedensides A (1) and C (3) have a conjugated double bond (22E,24-diene) in the side chain of the aglycon. Intercedenside B (2) has two beta-D-xylose and two sulfate groups in the carbohydrate chain. All three glycosides showed significant cytotoxicity against 10 human tumor cell lines with ED50 in the range 0.6-4.0 mug/mL. Intercedenside A (1) exhibited significant in vivo antineoplastic activity against mouse Lewis lung cancer and mouse S180 sarcoma. On the basis of these initially promising results, intercedensides A-C merit further study as potential anticancer agents.
引用
收藏
页码:1055 / 1060
页数:6
相关论文
共 8 条
[1]
Triterpene glycosides from the Far Eastern sea cucumber Pentamera calcigera II:: Disulfated glycosides [J].
Avilov, SA ;
Antonov, AS ;
Drozdova, OA ;
Kalinin, VI ;
Kalinovsky, AI ;
Riguera, R ;
Lenis, LA ;
Jiménez, C .
JOURNAL OF NATURAL PRODUCTS, 2000, 63 (10) :1349-1355
[2]
Kalinin V.I., 1996, Echinoderm Studies, V5, P139
[3]
Structure of eximisoside A, a novel triterpene glycoside from the far-eastern sea cucumber Psolus eximius [J].
Kalinin, VI ;
Avilov, SA ;
Kalinina, EY ;
Korolkova, OG ;
Kalinovsky, AI ;
Stonik, VA ;
Riguera, R ;
Jimenez, C .
JOURNAL OF NATURAL PRODUCTS, 1997, 60 (08) :817-819
[4]
A screening method for antimitotic and antifungal substances using conidia of Pyricularia oryzae, modification and application to tropical marine fungi [J].
Kobayashi, H ;
Namikoshi, M ;
Yoshimoto, T ;
Yokochi, T .
JOURNAL OF ANTIBIOTICS, 1996, 49 (09) :873-879
[5]
LIAO YL, 1997, CHINESE FAUNA ECHINO, P174
[6]
Two new cytotoxic and virucidal trisulfated triterpene glycosides from the antarctic sea cucumber Staurocucumis liouvillei [J].
Maier, MS ;
Roccatagliata, AJ ;
Kuriss, A ;
Chludil, H ;
Seldes, AM ;
Pujol, CA ;
Damonte, EB .
JOURNAL OF NATURAL PRODUCTS, 2001, 64 (06) :732-736
[7]
NEW COLORIMETRIC CYTOTOXICITY ASSAY FOR ANTICANCER-DRUG SCREENING [J].
SKEHAN, P ;
STORENG, R ;
SCUDIERO, D ;
MONKS, A ;
MCMAHON, J ;
VISTICA, D ;
WARREN, JT ;
BOKESCH, H ;
KENNEY, S ;
BOYD, MR .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1990, 82 (13) :1107-1112
[8]
Stonik V.A., 1988, Bioorganic Marine Chemistry, V2, P43