New cytotoxic prenylated isoflavonoids from Bituminaria morisiana

被引:37
作者
Cottiglia, F
Casu, L
Bonsignore, L
Casu, M
Floris, C
Leonti, M
Gertsch, J
Heilmann, J
机构
[1] Univ Cagliari, Fac Pharm, Dipartimento Farmaco Chim Tecnol, I-09124 Cagliari, Italy
[2] Univ Cagliari, Dipartimento Sci Chim, I-09124 Cagliari, Italy
[3] ETH, Swiss Fed Inst Technol, Inst Pharmaceut Sci, Dept Appl Biosci, CH-8093 Zurich, Switzerland
关键词
Bituminaria mosisiana; fabaceae; pterocarpans; isoflavones; cytotoxicity; necrosis;
D O I
10.1055/s-2005-837841
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Using cytotoxicity against KB cancer cells as a lead, bioguided-fractionation of the petroleum ether and ethyl acetate extracts of Bituminaria morisiana leaves led to the isolation of two new pterocarpans, namely 3,9-dihydroxy-4-(3,3-dimethylallyl) [6aR, 11aR]-pterocarpan, 3-hydroxy-4-(3,3-dimethylallyl)-4 '',5 ''-dehydropyrano[8,9:2 '',3 ''][6aR,11aR]-pterocarpan and one new isoflavone identified as 4 ',5 ''-dihydroxy-6 ''-methoxy-4 '',4 ''-dimethyl-4 '',5 ''-dihydro-6 '' H-pyrano[2 '',3 '':7,8]-isoflavone. Moreover, two known pterocarpans, erybraedin C and bitucarpin A, three known isoflavones, daidzein, 8-prenyldaidzein and bidwillon C, one known furocoumarin, pseudoisopsoralen and one known coumestan, coumestrol were isolated. The structures of the isolated compounds were established by means of 1D and 2D NMR spectroscopy, as well as mass spectrometry. Further cytotoxicity tests against cells related to the immune system (Jurkat T, Mono-Mac-6 and polymorphonuclear cells) showed a moderate activity of the known pterocarpan erybraedin C against all cell lines used (IC50 values between 17.6 - 28.8 mu M). In addition, erybraedin C was found to induce necrosis in leukaemia Jurkat T cells.
引用
收藏
页码:254 / 260
页数:7
相关论文
共 20 条
[1]  
Agrawal P.K., 1989, Carbon-13 NMR of Flavonoids
[2]   Influence of helenanolide-type sesquiterpene lactones on gene transcription profiles in Jurkat T cells and human peripheral blood cells: anti-inflammatory and cytotoxic effects [J].
Gertsch, J ;
Sticher, O ;
Schmidt, T ;
Heilmann, J .
BIOCHEMICAL PHARMACOLOGY, 2003, 66 (11) :2141-2153
[3]   Relative quantification of mRNA levels in Jurkat T cells with RT-real time-PCR (RT-rt-PCR):: New possibilities for the screening of anti-inflammatory and cytotoxic compounds [J].
Gertsch, J ;
Güttinger, M ;
Sticher, O ;
Heilmann, J .
PHARMACEUTICAL RESEARCH, 2002, 19 (08) :1236-1243
[4]   C-13-NMR SPECTRA AND CARBON-PROTON COUPLING-CONSTANTS OF VARIOUSLY ANNULATED FUROCOUMARINS [J].
GUIOTTO, A ;
MANZINI, P ;
CHILIN, A ;
PASTORINI, G ;
RODIGHIERO, P .
JOURNAL OF HETEROCYCLIC CHEMISTRY, 1985, 22 (03) :649-656
[5]   The influence of glutathione and cysteine levels on the cytotoxicity of helenanolide type sesquiterpene lactones against KB cells [J].
Heilmann, J ;
Wasescha, MR ;
Schmidt, TJ .
BIOORGANIC & MEDICINAL CHEMISTRY, 2001, 9 (08) :2189-2194
[6]   PHENOLIC-COMPOUNDS IN ERYTHRINA X BIDWILLII AND THEIR ACTIVITY AGAINST ORAL MICROBIAL ORGANISMS [J].
IINUMA, M ;
OKAWA, Y ;
TANAKA, T ;
KOBAYASHI, Y ;
MIYAUCHI, K .
HETEROCYCLES, 1994, 39 (02) :687-692
[7]   ANNEXIN-V FOR FLOW CYTOMETRIC DETECTION OF PHOSPHATIDYLSERINE EXPRESSION ON B-CELLS UNDERGOING APOPTOSIS [J].
KOOPMAN, G ;
REUTELINGSPERGER, CPM ;
KUIJTEN, GAM ;
KEEHNEN, RMJ ;
PALS, ST ;
VANOERS, MHJ .
BLOOD, 1994, 84 (05) :1415-1420
[8]   Hydrogen-atom abstraction/cyclization in synthesis. Direct syntheses of coumestan and coumestrol [J].
Kraus, GA ;
Zhang, N .
JOURNAL OF ORGANIC CHEMISTRY, 2000, 65 (18) :5644-5646
[9]  
Mabry T.J., 2012, SYSTEMATIC IDENTIFIC
[10]   H-1-NMR SPECTRA OF VARIOUSLY ANNULATED FUROCOUMARINS [J].
MANZINI, P ;
RODIGHIERO, P ;
CHILIN, A ;
GUIOTTO, A .
MAGNETIC RESONANCE IN CHEMISTRY, 1985, 23 (10) :875-876