• 제목/요약/키워드: Quercetin 3-methyl ether

검색결과 14건 처리시간 0.023초

Contribution to the Phytochemical Study of Egyptian Tamaricaceous Plants

  • Barakat, Heba H.
    • Natural Product Sciences
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    • 제4권4호
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    • pp.221-225
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    • 1998
  • A novel flavonol trisulphate, quercetin 7-methyl ether $3,3',4'-tri-O-KSO_3$ was isolated from the fresh leaves of Tamarix amplexicaulis (Tamaricaceae) along with the known flavonol mono sulphates, quercetin $3-O-KSO_3$ and quercetin 4'-methyl ether $3-O-KSO_3$. Structures were achieved through conventional analytical methods, including electrophoretic analysis and confirmed by FAB-MS and NMR spectroscopy.

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Sulphated Flavonols of the Flowers of Tamarix amplexicaulis

  • Souleman, Ahmed M.A.
    • Natural Product Sciences
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    • 제4권4호
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    • pp.215-220
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    • 1998
  • A new flavonol $3,5-di-O-KSO_3$:kaempferol 7,4'-dimethyl ether $3,5-O-KSO_3$, was isolated and identified from the flowers of Tamarix amplexicaulis. The known compounds quercetin $3-mono-O-KSO_3$, kaempferol 4'-methyl ether $3-mono-O-KSO_3$, kaempferol 7,4'-dimethyl ether $3-O-KSO_3$, quercetin 7,4'-dimethyl ether $3-mono-O-KSO_3$, kaempferol 3-O-glucuronide and quercetin 3-O-glucuronide were also separated and identified. Structures were established by conventional methods, including electrophoretic analysis, and confirmed by negative FAB-MS, $^1H-\;and\;^{13}C-NMR$.

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Constituents of the Stems and Fruits of Opuntia ficus-indica var. saboten

  • Lee, Eun-Ha;Kim, Hyoung-Ja;Song, Yun-Seon;Jin, Chang-Bae;Lee, Kyung-Tae;Cho, Jung-Sook;Lee, Yong-Sup
    • Archives of Pharmacal Research
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    • 제26권12호
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    • pp.1018-1023
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    • 2003
  • From the stems and fruits of Opuntia ficus-indica var. saboten, eight flavonoids, kaempferol (1), quercetin (2), kaempferol 3-methyl ether (3), quercetin 3-methyl ether (4), narcissin (5), (+)-dihydrokaempferol (aromadendrin, 6), (+)-dihydroquercetin (taxifolin, 7), eriodictyol (8), and two terpenoids, (6S,9S)-3-oxo-$\alpha-ionol-\beta$-D-glucopyranoside (9) and corchoionoside C (10) were isolated and identified by means of chemical and spectroscopic. Among these isolates, compounds 3∼5 and 8∼10 were reported for the first time from the stems and fruits of O. ficusindica var. saboten.

Polyphenolic Metabolites of the Flowers of Tamarix tetragyna

  • El-Mousallami, Amani M.D.;Hussein, Sahar A.M.;Nawwar, Mahmoud A.M.
    • Natural Product Sciences
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    • 제6권4호
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    • pp.193-198
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    • 2000
  • Phytochemical study of the constitutive polyphenolics of the flower aqueous alcohol extract of Tamarix tetragyna was carried out. The new sulphated flavonol, quercetin 3',4'-dimethyl ether $3-O-KSO_3$ as well as the new natural galloyl glucose, $2-O-galloyl-({\alpha}/{\beta})-^4C_1-glucopyranose$ were isolated and characterized. The known sulphated flavonols, kaempferol 7,4-dimethyl ether $3,5-di-O-KSO_3$, quercetin 7-methyl ether $3,3',4'-tri-O-KSO_3$, quercetin 7,4'-dimethyl ether $3-O-KSO_3$ and quercetin $3-O-KSO_3$ and the known sulphated phenolics, isoferulic acid $3-O-KSO_3$ and ellagic acid 4,4'-dimethyl ether $3-O-KSO_3$ were also separated and identified. The structures were established by conventional methods of analysis and confirmed by $^1H-,\;^{13}C-NMR$ and negative ESI-mass spectrometry. 2D-homonuclear chemical shift correlation NMR experiment was applied for the new natural galloylglucose.

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Acacia catechu의 플라보노이드 성분 (Flavonoid Constituents of Acacia catechu)

  • 홍성수;최윤혁;서화진;강민정;신정혜;권오운;오좌섭
    • Journal of Applied Biological Chemistry
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    • 제58권2호
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    • pp.189-194
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    • 2015
  • 전통생약으로서 다양한 효능과 염색제로서 사용되어온 A. catechu의 식물화학적 성분연구를 위해 열수추출물 중 ethyl acetate 분획으로부터 9종의 flavonoid와 1종의 tannin을 단리하였으며, 이들의 물리화학적 성상과 spectral data로부터 구조를 확인한 결과 (+)-catechin (1), (-)-epicatechin (2), (+)-afzelechin (3), (-)-epiafzelechin (4), (+)-mesquitol (5), kaempferol (6), quercetin (7), quercetin 3-methyl ether (8) caryatin (9) 및 ellagic acid (10)로 각각 확인 동정하였다. 이들 화합물 중 caryatin (9)은 Acacia 속으로부터 처음으로 분리되었다.

화분의 추출성분 (Extractives from Pollen)

  • 이상극;김진규;함연호;박재군;배영수
    • 임산에너지
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    • 제22권1호
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    • pp.30-36
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    • 2003
  • 화분을 98%의 EtOH로 추출하고 hexane, CH₂Cl₂, EtOAc, 그리고 H₂O용성으로 분획하여 동결건조 시켰다. 그 중에서 EtOAc 분획을 Sephadex LH-20으로 충진한 칼럼에서 MeOH와 EtOH-hexane혼합액을 용리용매로 사용하여 칼럼크로마토그래피를 실시하였다. 단리된 화합물들은 TLC로 확인한 후 NMR스펙트럼을 사용하여 정확한 구조규명을 하였고 FAB-MS로써 분자량을 측정하였다. 주로 quercetin-3-O-β-D-glucopyranoside와 kaempferol-3-O-β-D-rutinoside같은 flavonol 유도체들과 flavanonol계 화합물인 aromadendrin-5-methyl ether, 그리고 acid 화합물인 p-methoxybenzoic acid가 적은 양으로 단리 되었다.

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유산균 발효에 의한 손바닥선인장 줄기추출물의 지표물질 함량 변화 분석 (Analysis of Marker Components of Fermented Opuntia ficus-indica var. saboten Stem Extracts)

  • 신동원;이상호;이소연;한은혜
    • 분석과학
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    • 제31권6호
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    • pp.219-224
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    • 2018
  • 손바닥선인장(Opuntia ficus-indica var. saboten)은 제주도 자생식물로 섭취가 가능하고 항염 및 항산화, 인지개선 등 다양한 효능이 보고되었다. 본 연구에서는 손바닥선인장 줄기추출물의 지표물질 함량과 인지개선 효능을 높이기 위해 유산균 발효를 수행하였으며, 비발효추출물과 발효추출물 간 지표물질 함량 차이를 비교하고 acetylcholinesterase (AChE)의 저해 활성도를 평가하여 유산균 발효가 인지장애 개선에 미치는 효과를 연구하였다. 지표물질로는 손바닥선인장 줄기 중 함량이 높은 dihydrokaempferol(DHK)과 항산화 효능이 우수하다고 알려진 quercetin-3-methyl ether (3-MeQ)를 선정하였으며, 함량은 HPLC-PDA (280 nm, 360 nm)로 측정하였다. 실험 결과, 발효추출물의 DHK 함량은 비발효추출물에 비해 16.7 % 증가하였고, 3-MeQ 함량은 L. plantarum과 L. fermentum 발효추출물에서 각각 28.6 %, 21.4 % 증가하였다. 또한, 발효추출물의 AChE 저해 활성이 비발효추출물 ($IC_{50}=28.35mg/mL$)보다 높았으며, 발효추출물 중에서도 L. plantarum 발효추출물 ($IC_{50}=12.56mg/mL$)이 L. fermentum 발효추출물 ($IC_{50}=17.71mg/mL$)보다 높은 AChE 저해 활성을 보였다. 따라서 손바닥선인장 줄기추출물은 유산균 발효에 의해 지표성분 함량이 증가되었으며, AChE 저해 활성이 높아지고 이로 인해 인지장애 개선 효과가 나타난 것으로 사료된다. 이러한 결과는 효능이 향상된 고부가가치의 손바닥선인장 제품 개발에 유용한 자료로 활용될 수 있을 것이다.

하수오 지상부의 활성 성분 (Active Compounds from The Aerial Parts of Polygonum multiflorum Thunberg)

  • 김진표;김도훈;김기은;김진효;정성희;김성건;황완균
    • 약학회지
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    • 제50권6호
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    • pp.351-357
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    • 2006
  • Polygoni Radix (Polygonaceae) has been used as renal disoder hematopoietic, menstrual irregularity and antiaging in Korean folk medicine. Specially aerial parts has been used for insomnia and sedative agent. In order to investigate the efficacy of antioxidant activity on these aerial parts, the bio-activity guided fraction and isolation of physiologically active substance were performed. H$_2$O, 30%, 60%, 100% MeOH were examined antioxidant activity by DPPH method. It was revealed that 30%, 60% MeOH fractions have significantly antioxidant activity. From 60% MeOH fraction, six known flavonoid glycosides (quercetin, quercetin 3-O-${\beta}$-D-galactopyranosyl-4'-O-glucopyrano side-3'-methyl ether, quercetin 3-O-${\alpha}$-L-rhannopyranoside, quercetin 3-O- ${\alpha}$-L-rhamnopyranoside-4'-methylethor, quorcetin 3-O-${\beta}$-D-galactopyranoside, quercetin 3-O-${\beta}$-D-galactopyranoside) and 3,4-Oihydrocinnarnic acid were isolated. To investigate the antioxidant activities of each com-pounds, we measured radical scavening activity with DPPH method and anti-lipid peroxidative efficacy on low density lipo-protein (LDL) with TBARS assay and anti-acetylcholinestrase activity with Ellman's Test. Four compounds (ll, IV Vl, Vll) of quercetin glycosides showed significant activity.

Antioxidant Compounds from Distylium racemosum Leaves

  • Park, Youngki;Lee, Wi Young;Ahn, Jin Kwon;Lee, Hak-Ju;Chin, Hwi Seung;Kwon, Young Jin
    • Journal of the Korean Wood Science and Technology
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    • 제31권6호
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    • pp.67-72
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    • 2003
  • The leaves of D. racemosum showed strong DPPH (1,1-diphenyl-2-picrylhydrazyl) radical scavenging activity and the order of the radical scavenging activity against DPPH radical is ethyl acetate (EtOAc) fraction>crude extracts>residue fraction>hexane fraction>ether fraction, under the experimental conditions. Since EtOAc fraction has highest antioxidative activity among these fractions, the isolation was performed from the EtOAc fraction of the leaves of D. racemosum and four phenolic compounds were isolated and identified as follows: methyl gallate, kaempferol, quercetin and quercitrin. The free radical scavenging activities of these compounds were 79.9%, 93.1%, 93.6% and 66.7% at 10 ㎍/ml, respectively. The IC50 of compound 1, compound 2, compound 3 and compound 4 were 6.1, 4.1, 3.6 and 6.5 ㎍/ml, respectively. These compounds have higher antioxidative activity compared with reference compounds, ascorbic acid (IC50 = 9.6 ㎍/ml).