1976
DOI: 10.1007/bf00565203
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Flavonoids of Atraphaxis pyrifolia. IV

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Cited by 7 publications
(6 citation statements)
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“…These data demonstrated that 8 – 12 had a catechol B-ring instead of the pyrogallol moiety in 1 – 5 . The structures of 8 – 12 were reported previously, ,, and these compounds were identified as 8- O -β- d -glucopyranosyl-7- O -methyl-3- O -α- l -rhamnopyranosylgossypetin ( 8 ), 8- O -acetyl-7- O -methyl-3- O -α- l -rhamnopyranosylgossypetin ( 9 ), 7- O -methyl-3- O -α- l -rhamnopyranosylgossypetin ( 10 ), 8- O -acetyl-7- O -methylgossypetin ( 11 ), and 7- O -methylgossypetin ( 12 ).…”
Section: Resultsmentioning
confidence: 87%
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“…These data demonstrated that 8 – 12 had a catechol B-ring instead of the pyrogallol moiety in 1 – 5 . The structures of 8 – 12 were reported previously, ,, and these compounds were identified as 8- O -β- d -glucopyranosyl-7- O -methyl-3- O -α- l -rhamnopyranosylgossypetin ( 8 ), 8- O -acetyl-7- O -methyl-3- O -α- l -rhamnopyranosylgossypetin ( 9 ), 7- O -methyl-3- O -α- l -rhamnopyranosylgossypetin ( 10 ), 8- O -acetyl-7- O -methylgossypetin ( 11 ), and 7- O -methylgossypetin ( 12 ).…”
Section: Resultsmentioning
confidence: 87%
“…These were europetin 3- O -α- l -rhamnopyranoside ( 6 ), myricitrin ( 7 ), fisetinidol, gallocatechin ( 14 ), catechin, afzelechin ( 15 ), aromadendrin, epigallocatechin ( 16 ), epicatechin ( 17 ), nikoenoside ( 19 ), N - trans -feruloyldopamine ( 20 ), N - trans -feruloyltyramine ( 21 ), N - p - trans -coumaroyldopamine ( 22 ), N - p - trans -coumaroyltyramine ( 23 ), emodin 8- O -β- d -glucopyranoside, emodin 8- O -(6′- O -malonyl)­glucoside, , torachrysone 8- O -β- d -(6′- O -malonyl)­glucopyranoside, syringaresinol, dehydroconiferyl alcohol, 3,4,5-trimethoxyphenyl 1- O -β- d -glucopyranoside, and methyl syringate . Compounds 8 – 12 had been isolated previously by Russian research groups and were identified as 8- O -β- d -glucopyranosyl-7- O -methyl-3- O -α- l -rhamnopyranosylgossypetin ( 8 ), 8- O -acetyl-7- O -methyl-3- O -α- l -rhamnopyranosylgossypetin ( 9 ), 7- O -methyl-3- O -α- l -rhamnopyranosylgossypetin ( 10 ), 8- O -acetyl-7- O -methylgossypetin ( 11 ), , and 7- O -methylgossypetin ( 12 ) . These compounds were identified using NMR data based on a comparison with the data for compounds 1 – 5 .…”
Section: Resultsmentioning
confidence: 99%
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“…The immunomodulatory effects of phenols enhance immune responses against infections and diseases, and their use in wound healing and skin health applications is based on their ability to promote tissue repair and protect the skin from oxidative damage. The versatile pharmacological activities of phenols underscore their importance in preventive and therapeutic approaches to various health conditions [ 102 , 103 , 104 ].…”
Section: Bioactive Compounds From Four Atraphaxis ...mentioning
confidence: 99%
“…Flavonoid glycosides have been found to be the major components of Atraphaxis species [ 10 ]. Few early studies on the phytochemistry of A. pyrifolia leaves reported the compounds: 7- O -methylgossypetin-3- O -α- l -rhamnopyranoside [ 11 ], 7- O -methylluteolin 4’- O - β - d -glucofuranosyl-(1→6)- d -glucopyranoside [ 12 ]; 8-acetylmethylgossypetin 3- O -α- l -rhamnopyranoside (pyrifolin), its aglycone 8-acetyl-7-methylgossypetin (pyrifolidin), and 7-methylgossipetin 3- O -α- l -rhamnopyranoside (pyrifolinin) [ 13 ]; 7-methylgossypetin 8- β - d -glucopyranoside 3- O -α- l -rhamnopyranoside and 7-methylgossipetin 8- β - d -glucopyranoside [ 14 ].…”
Section: Introductionmentioning
confidence: 99%