Secondary metabolites from Asphodelus aestivus

被引:0
作者
Calis, Ihsan [1 ]
Birincioglu, S. Serap
Kirmizibekmez, Hasan
Pfeiffer, Bernhard
Heilmann, Joerg
机构
[1] Hacettepe Univ, Dept Pharmacognosy, Fac Pharm, TR-06100 Ankara, Turkey
[2] Adnan Menderes Univ, Fac Vet Med, Dept Pathol, TR-09016 Aydin, Turkey
[3] ETH Honggerberg, Inst Pharmaceut Sci, CH-8093 Zurich, Switzerland
[4] Univ Regensburg, Inst Pharm, Lehrstuhl Pharmazeut Biol, D-93053 Regensburg, Germany
来源
ZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES | 2006年 / 61卷 / 10期
关键词
Asphodelus aestivus; Liliaceae; secondary metabolites; acylated flavone C-glycosides; CALLUS-CULTURES; RAMOSUS TUBERS; C-GLYCOSIDES; ANTHRAQUINONES; FLAVONOIDS;
D O I
暂无
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Together with ten well known compounds, the quinic acid derivative chlorogenic acid, the nucleoside adenosine, two amino acids, tryptophan and phenylalanine, the anthraquinone derivatives, aloemodin, aloemodin acetate and chyrosphanol 1-O-gentiobioside, the flavon C-glycosides, isovitexin, isoorientin and isoorientin 4'-O-beta-glucopyranoside, as well as two new acylated isoorientin derivatives, 6 ''-O-(malonyl)-isoorientin and 6 ''-O-[(S)-3-hydroxy-3-methylglutaroyl]-isoorientin, were isolated from the water soluble part of the methanolic extract of the fresh leaves of Asphodelus aestivus. All compounds were structurally identified by spectroscopic methods, including UV, MS, and NMR (1D and 2D) spectroscopy. Among the compounds isolated, chlorogenic acid and isoorientin were found to be the main compounds of the methanolic extract.
引用
收藏
页码:1304 / 1310
页数:7
相关论文
共 50 条
  • [31] Secondary Metabolites from Tissue Cultures and Plant Parts of Zizyphus mauritiana Cultivars Gola and Seb
    Nag, T. N.
    Chouhan, N.
    I INTERNATIONAL JUJUBE SYMPOSIUM, 2009, 840 : 327 - 333
  • [32] EFFECTS OF SUPPRESSION APPLICATIONS ON SUMMER ASPHODEL (Asphodelus aestivus Brot.) DENSITY, BOTANICAL COMPOSITION, FORAGE YIELD AND QUALITY OF AEGEAN RANGELANDS
    Surmen, Mustafa
    Kara, Emre
    TURKISH JOURNAL OF FIELD CROPS, 2022, 27 (01) : 61 - 70
  • [33] Secondary metabolites from the leaves of Hymenocardia acida and their chemotaxonomic significance
    Nanfack, Arno Rusel Donfack
    Metiave, Ariane Audrey Sinze
    Dongmo, Faustine Leonie Mafodong
    Lateef, Mehreen
    Awouafack, Maurice Ducret
    Ngouela, Silvere Augustin
    Ali, Muhammad Shaiq
    Tene, Mathieu
    BIOCHEMICAL SYSTEMATICS AND ECOLOGY, 2024, 113
  • [34] Nitrate reductase activity (NRA) in Asphodelus aestivus Brot. (Liliaceae): distribution among organs, seasonal variation and differences among populations
    Sakar, Fatma Selcen
    Arslan, Huelya
    Kirmizi, Serap
    Guleryuz, Guercan
    FLORA, 2010, 205 (08) : 527 - 531
  • [35] Secondary metabolites from Sambueus ebulus
    Atay, Irem
    Kirmizibekmez, Hasan
    Goren, Ahmet Ceyhan
    Yesilada, Erdem
    TURKISH JOURNAL OF CHEMISTRY, 2015, 39 (01) : 34 - 41
  • [36] Secondary Metabolites from Sibiraea angustata
    Hu, Yang-Zhirong
    Zhang, Wan-Chang
    Zhang, Shuo
    Xie, Guang-Bo
    PHARMACOGNOSY MAGAZINE, 2018, 14 (58) : 525 - 527
  • [37] Secondary metabolites from Centaurea moesiaca
    Trendafilova, Antoaneta
    Todorova, Milka
    Bancheva, Svetlana
    BIOCHEMICAL SYSTEMATICS AND ECOLOGY, 2007, 35 (08) : 544 - 548
  • [38] Secondary metabolites from Paronychia argentea
    Braca, Alessandra
    Bader, Ammar
    Siciliano, Tiziana
    De Tommasi, Nunziatina
    MAGNETIC RESONANCE IN CHEMISTRY, 2008, 46 (01) : 88 - 93
  • [39] Secondary metabolites from Centaurea orphanidea
    Gousiadou, C
    Skaltsa, H
    BIOCHEMICAL SYSTEMATICS AND ECOLOGY, 2003, 31 (04) : 389 - 396
  • [40] Secondary metabolites from Potentilla argentea
    Tomczyk, Michal
    BIOCHEMICAL SYSTEMATICS AND ECOLOGY, 2006, 34 (10) : 770 - 773