1.Isolation and 13C-NMR reassignment of chrysoeriol from eurya ciliata Leaves
Journal of Medicinal Materials - Hanoi 2004;9(6):182-184
From the leaves of Eurya ciliata(Merr),Chrysoeriol, a flavonoide, was isolated.The 13C-NMR reassignment of Chrysoeriol is based on the analysis of 2D-NMR experiments
Flavonoids
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Plant Leaves
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isolation & purification
2.Studies on chemical constitutes of Phellinus igniarius.
Shun-yan MO ; Yong-chun YANG ; Jian-gong SHI
China Journal of Chinese Materia Medica 2003;28(4):339-341
OBJECTIVETo study the chemical constituents of Phellinus igniarius.
METHODCompounds were isolated by nomal phasc sillica gel and Al2O3 chromatography and reverse phase HPLC. Their structures were elucidated by spectroscopic methods including IR, MS and NMR.
RESULTFive flavonoids and two coumarins were isolated from Phellinus igniarius and their structures were identified as naringenin, sakuranetin, aromadendrin, folerogenin, eriodictyol, coumarin and scopoletin.
CONCLUSIONAll these compounds were obtained from this genus for the first time.
Flavanones ; chemistry ; isolation & purification ; Flavonoids ; chemistry ; isolation & purification ; Polyporaceae ; chemistry ; Scopoletin ; chemistry ; isolation & purification
3.Flavonoids of Lysimachia paridiformis var. stenophylla.
Yuanhu ZHANG ; Li HE ; Huanyu GUAN ; Jiming ZHANG ; Xiaosheng YANG
China Journal of Chinese Materia Medica 2010;35(14):1824-1826
Nine flavonoids were isolated and identified as luteolin (1), luteolin-4'-O-beta-D-glucoside (2), acacetin-7-O-beta-D-glucoside (3), rutin (4), acacetin (5), quercetin (6), quercetin-3-O-beta-D-glucoside (7), kaempferol-3-O-beta-D-glucoside (8), Isorhamnetin-3-O-beta-D-glucoside(9) from Lysimachia paridiformis var. stenophylla, and all these compounds were isolated from this plant for the first time.
Antioxidants
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analysis
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isolation & purification
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Drugs, Chinese Herbal
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analysis
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isolation & purification
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Flavonoids
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analysis
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isolation & purification
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Primulaceae
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chemistry
4.Flavonoids and nor-sesquiterpenes of Pedicularis densispica.
Hongbiao CHU ; Wenjun HE ; Yumei ZHANG ; Changjiu JI ; Ninghua TAN
China Journal of Chinese Materia Medica 2011;36(19):2672-2675
OBJECTIVETo study the chemical constituents of the whole plants of Pedicularis densispica.
METHODThe chemical constituents were isolated by various chromatographic methods and their structures were determined by chemical evidences and spectral data.
RESULTTen compounds were isolated and identified as acacetin (1), apigenin-7-0-beta-glucopyranoside (2), kaempferol-3,7-O-alpha-dirhamnopyranoside (3), scutellarein-7-0-beta-glucopyranoside (4), chrysoeriol-7-O-beta-glucopyranoside (5), pedicutricone A (6), dearabinosyl pneumonanthoside (7), salidroside (8), darendoside B (9), and maltol-beta-D-glucopyranoside (10).
CONCLUSIONThese compounds were isolated from the titled plant for the first time. Except compounds 6 and 8, the others were obtained for the first time from the genus Pedicularis.
Drugs, Chinese Herbal ; analysis ; isolation & purification ; Flavonoids ; analysis ; isolation & purification ; Pedicularis ; chemistry ; Sesquiterpenes ; analysis ; isolation & purification
5.A new antioxidant flavonoid glycoside from flowers of Hosta plantaginea.
Qing-Guang ZHOU ; Li YANG ; Jun-Wei HE ; Guo-Yue ZHONG
China Journal of Chinese Materia Medica 2019;44(15):3312-3315
Phytochemical investigation of the flowers of Hosta plantaginea led to isolate of one new flavonoid glycoside,plantanone C( 1) by silica gel,Sephadex LH-20,and RP-HPLC column chromatographies. Its structure was extensively determined on basis of HR-ESI-MS and NMR spectroscopic data. Compound 1 exhibited moderate antioxidant activity against DPPH radical scavenging activity,with an IC50 value of 240. 2 μmol·L~(-1).
Antioxidants
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analysis
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isolation & purification
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Flavonoids
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analysis
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isolation & purification
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Flowers
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chemistry
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Glycosides
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analysis
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isolation & purification
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Hosta
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chemistry
6.Flavonoids in leaves of Alstonia scholaris.
Tingting HUI ; Yun SUN ; Liping ZHU ; Wen GUO ; Gaoxiong RAO
China Journal of Chinese Materia Medica 2009;34(9):1111-1113
OBJECTIVETo investigate the flavonoids in leaves of Alstonia scholaris, an ethno-remedy of Dai People in Yunnan.
METHODThe chemical constituents were isolated and purified by column chromatography. Their structures were elucidated on the basis of spectroscopic evidences and physicochemical properties.
RESULTEight flavonoids were isolated and identified as kaempferol (1), quercetin (2), isorhamnetin (3), kaempferol-3-0-beta-D-galactopyranoside (4), quercetin-3-0-beta-D-galactopyranoside (5), isorhamnetin-3-0-beta-D-galactopyranoside (6), kaempferol-3-0-beta-D-xylopyranosyl-( 2-1)-0-beta-D-galactopyranoside (7) ,quercetin-3-0-beta-D-xylopyranosyl-( 2-1)-0-beta-D-galactopyranoside (8).
CONCLUSIONFlavonoids 1-7 were isolated from A. scholaris for the first time.
Alstonia ; chemistry ; Flavonoids ; analysis ; isolation & purification ; Plant Leaves ; chemistry
7.Flavonoids from roots of Flemingia philippinensis.
Hua LI ; Meihua YANG ; Xiaojun MA
China Journal of Chinese Materia Medica 2009;34(6):724-726
OBJECTIVETo investigate the chemical constituents of the roots of Flemingia philippinensis.
METHODSilica gel, ODS silica gel and Sephadex LH-20 column chromatography were employed for the isolation and purification. The structures were identified on the basis of spectral data (MS, 1H-NMR and 13C-NMR) and chemical evidence.
RESULTSeven compounds were isolated from the 75% ethanolic extract of the roots of F. philippinensis and identified as follows: flemiphilippinin D (1), dorsmanins I (2), osajin (3), eriosematin (4), lupinalbin A (5), genistein (6) and 3'-O-methylorobol (7).
CONCLUSIONThe compounds 2, 3 and 4 were isolated from the genus Flemingia for the first time. The compounds 2 and 4 were obtained from the Flemingia philippinensis for the first time.
Fabaceae ; chemistry ; Flavonoids ; analysis ; isolation & purification ; Plant Roots ; chemistry
8.Study on flavonoid chemical constituents contained in Memorialis hirta.
Jun LEI ; Yunchuan XIAO ; Wenjing WANG ; Zhen XI ; Miao LIU ; Jian RAN ; Jing HUANG
China Journal of Chinese Materia Medica 2012;37(4):478-482
OBJECTIVETo study the chemical constituents of Memorialis hirta.
METHODCompounds were isolated and purified by multiple methods, and their structures were identified based on physicochemical property and spectrum data.
RESULT12 compounds were isolated from ethyl acetate from 95% ethanol extracts of M. hirta, they were isorhamnetin (1), kaempferol (2), quercetin (3), isorhamnetin-3-O-alpha-L-rhamnopyranoside (4), kaempferol-3-O-alpha-L-rhamnopyranoside (5), isorhamnetin-3-O-beta-D-glucopyranoside (6), kaempferol-3-O-beta-D-glucopyranoside (7), quercetin-3-O-alpha-L-rhamnopyranoside (8), quercetin-3-O-beta-D-glucopyranoside (9), isorhamnetin-3-O-rutinoside (10), kaempferol-3-O-rutinoside (11) and quercetin-3-O-rutinoside (12), respectively.
CONCLUSIONAll compounds were obtained from the genus Memorialis for the first time.
Drugs, Chinese Herbal ; chemistry ; Flavonoids ; analysis ; isolation & purification ; Urticaceae ; chemistry
9.Study of reason of "the older, the better" of Pericarpium Citri Reticulatae (PCR) which contributed increase of flavonoids.
Fu WANG ; Xin ZHANG ; Jun-yu LU ; Guo-rong MEI ; Hong-ping CHEN ; Lin CHEN ; You-ping LIU
China Journal of Chinese Materia Medica 2015;40(24):4890-4896
This study is to explore the reason of "the older, the better" of PCR and itsincrease of flavonoids. We identified the fun- gus isolated from the PCR using microscopic and molecular identification. HPLC method was used to determine the content of 4 fla- vonoids and to clarifythe regularity of them; UV spectrophotometry method was used to determine the total content of flavonoids; reverse thinking was applied to screen the fungus that have close relation to the change of flavonoids. Finally, we have isolated and identified 25 fungusfrom the PCR, which belong to 2 genus and 4 species, including pencillium commune, P. minioluteeum, P. citrinum, Aspergillus flavus and A. niger. The content of flavonoids was increased in the mildew PCR due to A. niger and other fungus. Therefore, "the ol- der, the better" of PCR had its scientific reason that the increase of flavonoids had a close relation of the metabolic activity of A. niger and other fungus.
Citrus
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chemistry
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microbiology
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Flavonoids
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analysis
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Fungi
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isolation & purification
10.Studies on flavonoids from Derris eriocarpa.
Lun-xing WANG ; Hong-guo WU ; Hua ZHANG ; Hua-yong LOU ; Guang-yi LIANG ; Wen-wen JIANG ; Zai-chang YANG ; Wei-dong PAN
China Journal of Chinese Materia Medica 2015;40(15):3009-3012
Derris eriocarpa, a traditional Chinese medicine belonging to the family of Leguminosae, is widely distributed mainly over Yunnan, Guangxi and Guizhou of China. Modern pharmacological researches on this herb showed that it had extensive bioactivities, such as promoting urination, removing dampness and cough and reducing inspissated mucus and other biological activities. The extensive studies on the chemical constituents of this plant have resulted in the isolation of triterpenoids, steroids, fatty acid and others, but the flavone compounds haven't reported before. In our further research on the ethyl acetate of this plant, nine flavone compounds were obtained by column chromatography on silica gel, Sephadex LH-20, semi-prep HPLC, polyamide column chromatography and recrystallization for separation and purification. The structures were determined on the basis of extensive spectroscopic analysis, including MS, NMR experiments and comparison with spectroscopic data in the literature, respectively, as diosmetin (1), 3, 3'-di-O-methylquercetin (2), afromosin (3), 6, 3'-dihydroxy-7, 4'-dimethoxyisoflavone (4), odoratin (5), 7, 3'-dihydroxy-8, 4'-dimethoxyisoflavone (6), 6, 4'-dihydroxy-7, 3'-dimethoxyisoflavone (7), 5, 7, 4'-trihydroxy-3, 3', 5'-trimethoxyflavone (8), and alpinumisoflavone (9). All these compounds were isolated from Derris eriocarpa How for the first time. And the in vitro assays showed that compound 2 possessed moderate inhibitory activity against human cancer cells K562 and HEL.
Derris
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chemistry
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Flavonoids
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chemistry
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isolation & purification
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pharmacology
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Humans
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K562 Cells