Sesquiterpene Lactones and Flavonoids from the aerial parts of Anthemis melanolepis L

Planta Medica ◽  
2006 ◽  
Vol 72 (11) ◽  
Author(s):  
H Skaltsa ◽  
V Saroglou ◽  
Z Kypriotakis
Planta Medica ◽  
2007 ◽  
Vol 73 (09) ◽  
Author(s):  
V Saroglou ◽  
A Karioti ◽  
H Skaltsa

Foods ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 59
Author(s):  
Janusz Malarz ◽  
Klaudia Michalska ◽  
Anna Stojakowska

The objective of the present study was to characterize chemical composition of hitherto unexamined aerial parts of Lactuca sativa var. angustana cv. Grüner Stern. In contrast to leafy and head varieties of the lettuces, asparagus lettuce grown in Europe is much less studied. Fractionation of a methanolic extract from leaves of L. sativa cv. Grüner Stern, supported with HPLC/DAD and 1H NMR analysis, led to the isolation and/or identification of numerous terpenoid and phenolic compounds, including five apocarotenoids—(-)-loliolide, (+)-dehydrovomifoliol, blumenol A, (6S,9S)-vomifoliol, and corchoionoside C; three sesquiterpene lactones; two lignans—((+)-syringaresinol and its 4-O-β-glucoside); five caffeic acid derivatives; and three flavonoids. Some of the compounds, to the best of our knowledge, have never been isolated from L. sativa before. Moreover, monolignols, phenolic acids and a tryptophan-derived alkaloid were found in the analyzed plant material. Stems, leaves and shoot tips of the asparagus lettuce were examined to assess their phenolics and sesquiterpene lactone content as well as DPPH scavenging activity. Another stem lettuce—L. sativa var. angustana cv. Karola, two cultivars of leafy lettuces and one species of wild lettuce—L. serriola, were also examined as a reference material using HPLC/DAD. The results have been discussed regarding our previous studies and the literature data available.


ChemInform ◽  
2007 ◽  
Vol 38 (17) ◽  
Author(s):  
Hamad Hassan Issa ◽  
Sue-Ming Chang ◽  
Yu-Liang Yang ◽  
Fang-Rong Chang ◽  
Yang-Chang Wu

2010 ◽  
Vol 5 (5) ◽  
pp. 1934578X1000500 ◽  
Author(s):  
Humberto Takeshi Sakamoto ◽  
Eugênio Paceli Laudares ◽  
Antônio Eduardo Miller Crotti ◽  
Norberto Peporine Lopes ◽  
Walter Vichnewski ◽  
...  

Two new sesquiterpene lactones 8α-(2’,3’-dihydroxy-2’-methylbutanoyl)-15-desoxygoyazensolide and 16α-(1’,2’-dihydroxy-1’-methylpropyl)-eremantholide have been identified as constituents of Eremanthus argenteus aerial parts. In addition, two known sesquiterpene lactones and three flavonoids were isolated. Their structures were established on the basis of spectroscopic and spectrometric data.


2008 ◽  
Vol 71 (4) ◽  
pp. 678-683 ◽  
Author(s):  
Min Cheol Yang ◽  
Sang Un Choi ◽  
Wahn Soo Choi ◽  
Sun Yeou Kim ◽  
Kang Ro Lee

1992 ◽  
Vol 57 (5) ◽  
pp. 1092-1102 ◽  
Author(s):  
Ełżbieta Błoszyk ◽  
Urszula Rychłewska ◽  
Beata Szczepanska ◽  
Miloš Buděšínský ◽  
Bohdan Drożdż ◽  
...  

In addition to the already described peruvin (I), two further lactones, 3α-hydroxy-11αH,13-dihydrodamsin (II) and, 3α-acetoxy-11αH,13-dihydrodamsin (III), were isolated from aerial parts of species Ambrosia artemisiifolia L. The full structure of these lactones was derived from their NMR and CD spectra and the X-ray structural analysis of compound III. In the aerial part of Ambrosia trifida L. species coronopilin (V) and ivoxanthin (VI) were also identified.


2013 ◽  
Vol 68 (5-6) ◽  
pp. 175-180
Author(s):  
Abou El-Hamd H. Mohamed ◽  
Hosam-Eldin H. Mahmoud ◽  
Fathy F. Abdellatif ◽  
Yousif S. Mohamed ◽  
Ahmed A. Ahmed

The aerial parts of Inula verbascifolia afforded two new guaianolide-type sesquiterpene lactones. Their structures were determined by spectroscopic methods (IR, MS, 1H NMR, 13C NMR, DEPT, 1H-1H COSY, HMQC, and HMBC).


Molecules ◽  
2020 ◽  
Vol 25 (13) ◽  
pp. 3005
Author(s):  
Lhaís Araújo Caldas ◽  
Mariana T. Rodrigues ◽  
Andrea N. L. Batista ◽  
João M. Batista ◽  
João H. G. Lago ◽  
...  

This work describes the chromatographic fractionation of the aerial parts of Calea pinnatifida and the structural characterization and determination of the absolute configuration of the isolated compounds as well as their antitumor potential. The HPLC fractionation of the CH2Cl2 phase of the MeOH extract from the leaves of C. pinnatifida led to the isolation of two related sesquiterpene lactones (STLs): calein C (1) and calealactone B (2). Additionally, during the purification process, a derivative of calein C (3) was formed as a product of the Michael addition of MeOH. The structures of Compounds 1–3 were established based on spectroscopic and spectrometric data, while the absolute stereochemistry was established by vibrational circular dichroism. In order to evaluate the effect of the conjugated double bonds on the cytotoxic activity of STLs, Compounds 1–3 were tested against anaplastic (KTC-2) and papillary (TPC-1) thyroid carcinoma cells. Calein C was the most active of the STLs, and displayed activity against both KTC-2 and TPC-1. On the other hand, the calein C derivative (3) was the least cytotoxic of all the compounds tested. These results are promising and suggest the importance of studying sesquiterpene lactones isolated from C. pinnatifida in terms of antitumor activity, especially considering the effects of α,β-unsaturated carbonyl systems.


Planta Medica ◽  
2013 ◽  
Vol 79 (08) ◽  
pp. 661-665 ◽  
Author(s):  
Lun Wang ◽  
Jing Wang ◽  
Fu Li ◽  
Xin Liu ◽  
Bin Chen ◽  
...  

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