New Triterpenic Saponins from the Aerial Parts of Medicago arabica (L.) Huds

被引:42
作者
Tava, Aldo [1 ]
Mella, Mariella [2 ]
Avato, Pinarosa [3 ]
Biazzi, Elisa [1 ]
Pecetti, Luciano [1 ]
Bialy, Zbigniew [4 ]
Jurzysta, Marian [4 ]
机构
[1] CRA FLC, Ctr Ric Prod Foraggere & Lattiero Casearie, I-26900 Lodi, Italy
[2] Univ Pavia, Dipartimento Chim Organ, I-27100 Pavia, Italy
[3] Univ Bari, Dipartimento Farmacochim, I-70125 Bari, Italy
[4] Inst Soil Sci & Plant Cultivat, Dept Biochem, PL-24100 Pulawy, Poland
关键词
Medicago arabica L. Huds; saponins; chemical structure; triterpene glycosides; queretaroic acid; ESI-MS/MS; NMR; QUERETAROIC ACID; ANTIMICROBIAL ACTIVITY; MASS SPECTROMETRY; OLEANOLIC ACID; GLYCOSIDES; SAPOGENINS; EXTRACTS; LEAVES; CACTUS; ROOT;
D O I
10.1021/jf8036984
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
The reinvestigation of saponin composition from Medicago arabica from Italy allowed the detection of nineteen (1-19) saponins. All of them were purified by reverse-phase chromatography and their structures elucidated by spectroscopic and spectrometric (1D and 2D NMR; ESI-MS/MS) and chemical methods. Fourteen were known saponins, previously found in other plants including other Medicago, species. They have been identified as glycosides of oleanolic acid, 2 beta,3 beta-dihydroxyolean-12-en-28-oic acid, hederagenin, bayogenin and soyasapogenol B. Five saponins, identified as 3-O-[-alpha-L-arabinopyranosyl(1 -> 2)-beta-D-glucuronopyranosyl]-30-O-beta-D-glucopyranosyl 2 beta,3 beta,30-trihydroxyolean-12-en-28-oic acid (1), 3-O-[alpha-L-arabinopyranosyl(1 -> 2)-beta- -D-glucuronopyranosyl]-30-O-[beta-D-glucopyranosyl]3 beta,30-dihydroxyolean-12-en-28-oic acid (2), 3-O-[beta-D-glucuronopyranosyl]-30-O-[alpha-L-arabinopyranosyl(1 -> 2)-beta-D-glucopyranosyl]2 beta,3 beta,30-trihydroxyolean-12-en-28-oic acid (3), 3-O-[beta-D-glucuronopyranosyl]-30-O[alpha-L-arabinopyranosyl(1 -> 2)-beta-D-glucopyranosyl] 3 beta,30-dihydroxyolean-12-en-28-oic acid (4) and 3-O-[beta-D-glucuronopyranosyl]-30-O-[beta-D-glucopyranosyl] 2 beta,3 beta,30-trihydroxyolean-12-en-28-oic acid (5), are reported here as new natural compounds. These new saponins, possessing a hydroxy group at the 30-methyl position of the triterpenic skeleton, have never been previously found in the genus Medicago.
引用
收藏
页码:2826 / 2835
页数:10
相关论文
共 34 条
[1]   Antimicrobial activity of Saponins from Medicago sp.:: Structure-activity relationship [J].
Avato, Pinarosa ;
Bucci, Rossella ;
Tava, Aldo ;
Vitali, Cesare ;
Rosato, Antonio ;
Bialy, Zbigniew ;
Jurzysta, Marian .
PHYTOTHERAPY RESEARCH, 2006, 20 (06) :454-457
[2]   Triterpene saponins from the roots of Medicago hybrida [J].
Bialy, Z ;
Jurzysta, M ;
Mella, M ;
Tava, A .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2006, 54 (07) :2520-2526
[3]   Triterpene Saponins from aerial parts of Medicago arabica L. [J].
Bialy, Z ;
Jurzysta, M ;
Mella, M ;
Tava, A .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2004, 52 (05) :1095-1099
[4]   Saponins in alfalfa (Medicago sativa L.) root and their structural elucidation [J].
Bialy, Z ;
Jurzysta, M ;
Oleszek, W ;
Piacente, S ;
Pizza, C .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 1999, 47 (08) :3185-3192
[5]   MASS SPECTROMETRY IN STRUCTURAL AND STEREOCHEMICAL PROBLEMS .32. PENTACYCLIC TRITERPENES [J].
BUDZIKIEWICZ, H ;
WILSON, JM ;
DJERASSI, C .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1963, 85 (22) :3688-&
[6]   GAS CHROMATOGRAPHY-MASS SPECTROMETRY OF OLEANANE-TYPE AND URSANE-TYPE TRITERPENES - APPLICATION TO CHENOPODIUM-QUINOA TRITERPENES [J].
BURNOUFRADOSEVICH, M ;
DELFEL, NE ;
ENGLAND, R .
PHYTOCHEMISTRY, 1985, 24 (09) :2063-2066
[7]   TERPENOIDS .24. THE STRUCTURE OF THE CACTUS TRITERPENE QUERETAROIC ACID [J].
DJERASSI, C ;
HENRY, JA ;
LEMIN, AJ ;
RIOS, T ;
THOMAS, GH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1956, 78 (15) :3783-3787
[8]   Triterpene glycosides from Cussonia paniculata.: III.: Structure of glycosides I1, I2, J1a, J1b, J2, K, L1, and L2 from C-paniculata leaves [J].
Dovgii, I. I. ;
Grishkovets, V. I. ;
Kachala, V. V. ;
Shashkov, A. S. .
CHEMISTRY OF NATURAL COMPOUNDS, 2006, 42 (02) :182-185
[9]   Hydroxylation of oleanolic acid to queretaroic acid by cytochrome p450 from Nonomuraea recticatena [J].
Fujii, Yoshikazu ;
Hirosue, Shinji ;
Fujii, Tadashi ;
Matsumoto, Naoki ;
Agematu, Hitosi ;
Arisawa, Akira .
BIOSCIENCE BIOTECHNOLOGY AND BIOCHEMISTRY, 2006, 70 (09) :2299-2302
[10]   Antidermatophyte activity of medicago extracts and contained saponins and their structure-activity relationships [J].
Houghton, P. ;
Patel, N. ;
Jurzysta, M. ;
Biely, Z. ;
Cheung, C. .
PHYTOTHERAPY RESEARCH, 2006, 20 (12) :1061-1066