Planta Medica, Inhaltsverzeichnis Planta Med 2004; 70(6): 556-560DOI: 10.1055/s-2004-827157 Original PaperNatural Product Chemistry© Georg Thieme Verlag KG Stuttgart · New YorkSteroidal Saponins from Myriopteron extensum and Their Cytotoxic Activity Ming-Fu Yang1 , 2 , Yu-Yuan Li1 , Xiao-Ping Gao3 , Bo-Gang Li1 , 3 , Guo-Lin Zhang1 1Chengdu Institute of Biology, the Chinese Academy of Sciences, Chengdu, P. R. China 2Chengdu Institute of Organic Chemistry, the Chinese Academy of Sciences, Chengdu, P. R. China 3Pharmaceutical Institute of Di-Ao Pharmaceutical Group, Chengdu, P. R. China Artikel empfehlen Abstract Artikel einzeln kaufen Abstract Two new steroidal saponins, extensumsides A (1) and B (2), were isolated from the whole plants of Myriopteron extensum (Wight) K. Schum. Their structures were elucidated as 17β-uzarigenin-3-O-β-glucopyranosyl-(1→6)-β-glucopyranosyl-(1→4)-β-thevetopyranosyl-(1→4)-β-cymaropyranoside (1) and 12-(3-methylbut-2-enoyloxy)pregn-5-en-20-one 3-O-[β-cymaropyranosyl-(1→4)-β-cymaropyranosyl-(1→4)-β-thevetopyranosyl-(1→4)-(6-O-sulfo-β-glucopyranoside)] (2) on the basis of chemical and spectral evidence. Extensumside A exhibited significant cytotoxicity against eight cancer cell lines with a mean GI50 value of 0.346 μg/mL. Key words Myriopteron extensum - Asclepiadaceae - cytotoxic activity - extensumside A - extensumside B Volltext Referenzen References 1 Delectis Florae Reipublicae Popularis Agendae Academiae Sinicae E dita. Flora Reipublicae Popularis Sinicae. Vol 63 Beijing; Science Press 1977: pp 270-2 2 Ran X D. Zhongyao Yaohai (Dictionary of Traditional Chinese Medicine). Vol 2 Harbin; Harbin Press 1993: p 1437 3 Sevillano L G, Melero C P, Caballero E, Tomé F, Lelièvre L G, Geering K. et al . Inotropic activity of hydroindene amidinohydrazones. J Med Chem. 2002; 45 127-36 4 Florkiewicz R Z, Anchin J, Baird A. The inhibition of fibroblast growth factor-2 export by cardenolides implies a novel function for the catalytic subunit of Na+,K+-ATPase. J Biol Chem. 1998; 273 544-51 5 Skehan P, Storing R, Scudiero D, Monk A, McMahon J, Visica D. et al . New colorimetric cytotoxity assay for anticancer-drug-screen. J Natl Cancer Inst. 1990; 82 1107-12 6 Rubinstein L V, Shoemaker R H, Paul K D, Tosini S, Skehan P, Scudiero D A. et al . Comparison of in vitro anticancer-drug-screening data generated with a tetrazolium assay versus a protein assay against a diverse panel of human tumor cell lines. J Natl Cancer Inst. 1990; 82 1113-8 7 Chen J J, Zhang Z X, Zhou J, Li B T. New pregnane glycosides from Sinomarsdenia incisa . J Nat Prod. 1999; 62 829-32 8 Hesham E A, Josef H, Sayed H, Elsayada E K. Cardenolide glycosides with doubly linked sugars from Gomphocarpus sinaicus . Phytochemistry. 1993; 34 1399-402 9 Maier M S, Roccatagliata A J, Kuriss A, Chludil H, Seldes A M, Pujol C A. et al . Two new cytotoxic and virucidal trisulfated triterpene glycosides from the Antarctic sea cucumber Staurocucumis liouvillei . J Nat Prod. 2001; 64 732-6 10 Abbott A J, Holoubek C G, Martin R A. Inhibition of Na+,K+-ATPase by the cardenolide 6′-O-(E-4-hydroxycinnamoyl)desglucouzarin. Biochem Biophys Res Commun. 1998; 251 256-9 11 Choiu F CK, Watson T R. Conformational factors in cardiac glycoside activity. J Med Chem. 1985; 28 509-15 12 Chen K K. Newer cardiac glycosides and aglycones. J Med Chem. 1970; 13 1029-34 13 Koike K, Bevelle C, Talapatra S K, Cordell G A, Farnsworth N R. Potential anticancer agents. V. Cardiac glycosides of Asclepias albicans (Asclepiadaceae). Chem Pharm Bull. 1980; 28 401-5 14 Hyun J W, Shin J E, Lim K H, Sung M S, Park J W, Yu J H. et al . Evomonoside: the cytotoxic cardiac glycoside from Lepidium apetalum . Planta Med. 1995; 61 294-5 Prof. Dr. Guo-Lin Zhang Chengdu Institute of Biology The Chinese Academy of Sciences P. O. Box 416 Chengdu 610041 P. R. China Telefon: +86-28-8522-5401 Fax: +86-28-8522-5401 eMail: zhanggl@cib.ac.cn