نتایج جستجو برای: flavone

تعداد نتایج: 1367  

Journal: :Zeitschrift fur Naturforschung. C, Journal of biosciences 2013
Judith L Nantchouang Ouete Louis P Sandjo Deccaux W F G Kapche Johannes C Liermann Till Opatz Ingrid K Simo Bonaventure T Ngadjui

A new flavonoid identified as 2-(2,4-dihydroxyphenyl)-5-hydroxy-8,8-dimethyl-4H,8H-pyrano[2,3-f]chromen-4-one (2'-hydroxyatalantoflavone) (1) was obtained from the roots of Milicia excelsa along with five known compounds including atalantoflavone (2), neocyclomorusin (3), 6-geranylnorartocarpetin (4), cudraxanthone I (5), and betulinic acid (6). The structures of the isolates were established o...

Journal: :Bulletin of environmental contamination and toxicology 2008
Guomei Li Yi Shi Xin Chen

C(3) crops are generally considered more sensitive than C(4) crops to the elevated CO(2) and O(3), but it is unclear whether the concentrations of phenolic compounds in them are affected. In this paper, an enrichment experiment with open-top chamber was conducted to examine the effects of elevated CO(2), O(3), and their combination on the contents of total phenolic compounds and flavone in the ...

2014
P. K. SAHU

The present work deals with the isolation and structure elucidation of new flavones from methanol extract of Avicennia alba aerial parts. Isolation of the compound was carried out by chromatographic techniques, followed by different spectral analytical methods. The spectral data of UV-Vis, FT-IR, 1H NMR, 13C NMR and GC-MS of the isolated compound is in support of presence of flavone nucleus. Th...

Journal: :Plant physiology 2007
Juan Zhang Senthil Subramanian Yansheng Zhang Oliver Yu

Flavones are important copigments found in the flowers of many higher plants and play a variety of roles in plant adaptation to stress. In Medicago species, flavones also act as signal molecules during symbiotic interaction with the diazotropic bacterium Sinorhizobium meliloti. They are the most potent nod gene inducers found in root exudates. However, flavone synthase II (FNS II), the key enzy...

Journal: :RSC advances 2014
Yi Luan Yue Qi Jie Yu Hongyi Gao Scott E Schaus

A novel HAuCl4@UiO-66-NH2 material has been obtained and utilized as a heterogeneous Au(III) catalyst. This Au(III) catalyst was able to promote the formation of a variety of dihydrochalcones starting from 2H-chromenes in moderate to good yields. A tandem hydride shift/hydration reaction sequence has been proposed based on deuterium labeling studies, which revealed a 1,5-hydride shift reaction ...

Journal: :Journal of virology 1987
J L Castrillo L Carrasco

3-Methylquercetin is a natural flavone that powerfully blocks poliovirus replication. This compound inhibits selectively poliovirus RNA synthesis both in infected cells and in cell-free systems. Poliovirus double-stranded RNA (replicative forms) is still made in the presence of this inhibitor, whereas the synthesis of single-stranded RNA and the formation of replicative intermediates are drasti...

Journal: :Zeitschrift fur Naturforschung. C, Journal of biosciences 2002
Sonia Piacente Ely E S Camargo Aurelia Zampelli Juliano S Gracioso Alba R Souza Brito Cosimo Pizza Wagner Vilegas

The infusion of the aerial parts of Turnera diffusa was phytochemically examined. Chromatographic procedures led to the isolation of a new flavone glycoside, five known flavonoids and p-arbutin. Structures were determined by 1D- and 2D NMR experiments, as well as ES-MS and UV spectra.

Journal: :Organic & biomolecular chemistry 2012
Marco V Mijangos Joaquin González-Marrero Luis D Miranda Paulette Vincent-Ruz Armando Lujan-Montelongo Diana Olivera-Díaz Elhiu Bautista Alfredo Ortega María de la Luz Campos-González Rocio Gamez-Montaño

Flavones were directly alkylated at the C-3 position in moderate yields using a xanthate-based oxidative radical addition procedure. This methodology is a suitable synthetic tool for the direct substitution of the vinylic and unactivated C-H bond of the C ring of the flavone by an alkyl functionality under neutral conditions.

Journal: :Journal of the Brazilian Chemical Society 2004

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