1974
DOI: 10.1016/0031-9422(74)80253-0
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Prunin-0-6″-gallat, aus Acacia farnesiana

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Cited by 16 publications
(5 citation statements)
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“…The Et 2 O layer was partitioned between hexane and MeOH, and the MeOH layer was further chromatographed successively over Sephadex LH-20, silica gel, MCI-gel CHP 20P and Chromatorex ODS to afford 1 and 2, as well as 17 known compounds. The known ones were identified as naringenin, 6) eriodictyol, 6) kaempferol, 7) dihydrokaempferol, 8,9) quercetin, 7) naringenin 7-O-glucoside (prunin), 10) naringenin 7-O-(6Љ-O-galloyl)-glucoside, 10) naringenin 7-O-(6Љ-O-trans-p-coumaroyl)-glucoside, 11) kaempferol 3-O-rhamnoside, 7) quercetin 3-O-rhamnoside, 7) myricetin 3-O-rhamnoside, 7) 2-(2-methylbutyryl)-phloroglucinol 1-O-b-D-glucopyranoside (multifidol glucoside) (5), 12) (Ϫ)-epigallocatechin 3-O-gallate, 13) 1,2,3,6-tetra-O-, 14) 1,2,4,6-tetra-O-, 15) and 1,2,3,4,5-penta-O-galloyl-b-Dglucose, 16) and decarboxyellagic acid 17) by comparison of the physical and spectral data with literature values.…”
Section: Resultsmentioning
confidence: 99%
“…The Et 2 O layer was partitioned between hexane and MeOH, and the MeOH layer was further chromatographed successively over Sephadex LH-20, silica gel, MCI-gel CHP 20P and Chromatorex ODS to afford 1 and 2, as well as 17 known compounds. The known ones were identified as naringenin, 6) eriodictyol, 6) kaempferol, 7) dihydrokaempferol, 8,9) quercetin, 7) naringenin 7-O-glucoside (prunin), 10) naringenin 7-O-(6Љ-O-galloyl)-glucoside, 10) naringenin 7-O-(6Љ-O-trans-p-coumaroyl)-glucoside, 11) kaempferol 3-O-rhamnoside, 7) quercetin 3-O-rhamnoside, 7) myricetin 3-O-rhamnoside, 7) 2-(2-methylbutyryl)-phloroglucinol 1-O-b-D-glucopyranoside (multifidol glucoside) (5), 12) (Ϫ)-epigallocatechin 3-O-gallate, 13) 1,2,3,6-tetra-O-, 14) 1,2,4,6-tetra-O-, 15) and 1,2,3,4,5-penta-O-galloyl-b-Dglucose, 16) and decarboxyellagic acid 17) by comparison of the physical and spectral data with literature values.…”
Section: Resultsmentioning
confidence: 99%
“…Ion at m/z 433 and 447 fragmented in MS/MS to produce ion that corresponded to standard quercetin, neural loss of 132 and 146 from each ion, respectively demonstrating presence of pentoside and deoyhexoside. [49] Thus, peaks 3 and 4 were tentatively identified as quercetin-pentoside and quercetin-deoxyhexoside. Peak 5 was tentatively identified as diosmetin-diglycoside based on the deprotonated ion [M-H]at m/z 607.…”
Section: Acknowledgementmentioning
confidence: 98%
“…Different parts of the plant have been used for the treatment of various ailments (Sahu et al, 1998). Previous chemical investigation on the flowers and pods of the plant have revealed the presence of four homoterpene lactones, flavone glycosides and several polyphenolic compounds (El Sissi et al, 1974). Its leaves are also consumed by livestock and white-tailed deer (Ramirez et al, 1995).…”
Section: Introductionmentioning
confidence: 99%