1990
DOI: 10.1016/0031-9422(90)85056-l
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Isoflavonoids and a cinnamyl phenol from root extracts of Erythrina variegata

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Cited by 46 publications
(25 citation statements)
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“…Além disto, este gênero tem provado ser uma fonte farta de espécies contendo agentes antimicrobianos que pertencem a várias classes estruturais de fl avonóides, como por exemplo, a E. variegata cuja atividade do extrato bruto das raízes foi demonstrada para Staphyloccus aureus e Mycobacterium smegmatis (Telikepalli et al, 1990).…”
Section: Introductionunclassified
“…Além disto, este gênero tem provado ser uma fonte farta de espécies contendo agentes antimicrobianos que pertencem a várias classes estruturais de fl avonóides, como por exemplo, a E. variegata cuja atividade do extrato bruto das raízes foi demonstrada para Staphyloccus aureus e Mycobacterium smegmatis (Telikepalli et al, 1990).…”
Section: Introductionunclassified
“…The two methylene groups at G 2.86 are typical of the ethane bridge in bibenzylic compounds [12]. According to the 1 H and 13 C data, a bibenzyl skeleton with one hydroxyl, one acetyl, one prenyl, and three O-methyl groups was deduced [13]. The signal at G C 112.4 is assigned to the nonprotonated carbon atom C-4c, based on correlations to the two-proton singlet at G H 6.43 (H-2c, H-6c) as well as due to the correlation of C-4c to the two-proton doublet at G H 3.31 (H-7c); C-4c was identified as the site of attachment of the prenyl group.…”
mentioning
confidence: 99%
“…The following compounds were isolated from the roots: warangalone (scandenone), 5,7,4′-trihydroxy-6,8-diprenylisofl avone, erycristagallin, erythrabys-sin-II, phaseollin, phaseollidin, isobavachin and a cinnamylphenol, eryvariestyrene ( E -1-[2, 4-dihydroxy-5-(3-m e t h y l bu t -2 -e ny l ) ] -2 -p h e ny l e t h y l e n e ) (Telikepalli et al 1990 ); pterocarpans, dihydrofolinin and erythrabyssin II, and the alkyl ester of ferulic acid, octacosyl ferulate (Ahmad et al 2002 ); orientanol B (9-hydroxy3-methoxy-2γ, (Sato et al 2002 ); two diphenylpropan-1,2-diols, eryvarinols A (1) and B (2) and their structures were elucidated as 1-(4-hydroxy-2-methoxyphenyl)-2-(4-hydroxy-3, 5-dimethoxybenzoyloxy)-3-(4-hydroxyphenyl) propan-1-ol (1) and its 3″-prenyl derivative (2) (Tanaka et al 2002a ); 3,9-dihydroxy-2,10-di(γ,γ-dimethylallyl)-6α,11α-dehydropterocarpan (erycristagallin) and 9-hydroxy-3-methoxy-2-γ,γ-dimethylallylpterocarpan (orientanol B) (Tanaka et al 2002b ); two 3-phenoxychromones, eryvarins F and G, and their structures were elucidated as 3-(2,4-dihydroxyphenoxy)-7-hydroxy-6,8-di (3,3-dimethylallyl)chromen-4-one and 3-(2,4-dihydroxyphenoxy)-8-(3,3-dimethylallyl)-2, 2-dimethylpyrano [5,6:6,7] chromen-4-one, respectively (Tanaka et al 2003 ); three isofl avonoids, eryvarins M-O, two 2-arylbenzofurans, eryvarins P and Q, and a 3-aryl-2,3-dihydrobenzofuran, eryvarin R ; two isofl avonoids, eryvarins S and T, and a new 2-arylbenzofuran, eryvarin U (Tanaka et al 2005 ); a biisofl avonoid, biseryvarin A, was isolated from the roots (Tanaka et al 2010 ); and two isofl avonoids, eryvarins V and W, and a chromen-4-one derivative, eryvarin X (Tanaka et al 2011 ).…”
Section: Root Phytochemicalsmentioning
confidence: 99%