• 제목/요약/키워드: Leguminosae 3′

검색결과 168건 처리시간 0.027초

Chemical Components from the Stems of Pueraria lobata and Their Tyrosinase Inhibitory Activity

  • Morgan, Abubaker M.A.;Jeon, Mi Ni;Jeong, Min Hye;Yang, Seo Young;Kim, Young Ho
    • Natural Product Sciences
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    • 제22권2호
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    • pp.111-116
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    • 2016
  • Phytochemical investigation of the stems of Pueraria lobata (Wild) Ohwi (Leguminosae), led to the isolation of eighteen known compounds: ${\beta}$-amyrone (1), (+)-pinoresinol (2), (+)-syringaresinol (3) $(+)-syringaresinol-O-{\beta}-{\small{D}}-glucoside$ (4), (+)-lariciresinol (5), (-)-tuberosin (6), naringenin (7), liquiritigenin (8), isoliquiritigenin (9) genistein (10), daidzein (11) daidzin (12) daidzein 4',7-diglucoside (13) 2,4,4'-trihydroxy deoxybenzoin (14), S-(+)-1-hydroxy-3-(4-hydroxyphenyl)-1-(4-hydroxy-2-methoxy-phenyl)propan-2-one (15), methyl $2-O-{\beta}-{\small{D}}-glucopyranosylbenzoate$ (16), pyromeconic acid $3-O-{\beta}-{\small{D}}-glucopyranoside$ 6'- (O-4''-hydroxy-3-methoxybenzoate) (17), and allantion (18). The chemical structures of these compounds were elucidated from spectroscopic data and by comparison of those data with previously published results. The effects of isolated compounds on mushroom tyrosinase enzymatic activity were screened. The results indicated that, chloroform extract of P. lobata stems turned out to be having tyrosinase inhibitory effect, and only compounds 5, 8, 9, and 11 showed enzyme inhibitory activity, with $IC_{50}$ values of $21.49{\pm}4.44$, $25.24{\pm}6.79$, $4.85{\pm}2.29$, and $17.50{\pm}1.29{\mu}M$, respectively, in comparison with these of positive control, kojic acid ($IC_{50}\;12.28{\pm}2.72{\mu}M$). The results suggest that P. lobata stems extract as well as its chemical components may represent as potential candidates for tyrosinase inhibitors.

제주도내 6개부락 공동목장 야초지에 대한 방목기의 건물수량 , 일반조성분 및 식생구성율의 변화 (Changes in Dry Matter Yield , Chemical Composition , Botanical Composition of Native Pasture during the Grazing Period at Six Co-operative Village Farms Situated)

  • 김문철;김동암
    • 한국초지조사료학회지
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    • 제4권2호
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    • pp.152-157
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    • 1983
  • 濟州道內 6個部落 共同牧場 野草地를 對象으로 野草의 生産性과 植生比率이 家畜 增體에 미치는 效果를 究明하기 위해 1981년 5월부터 동년 11월까지 調査, 分析한 結果는 다음과 같다. 1. 乾物收量은 7月收穫보다 10月收穫에서 2培二上 높았으며 모든 牧場이 같은 趨勢였다. 2. 野草의 祖蛋白質 含量은 7월보다 10월에서 낮았으며 粗纖維는 그 반대였다. 3. 牧場別로 볼 때 1일 增體量이 높은 河源과 海安牧場이 野草의 組蛋白質 含量이 가장 높았고 增體率이 제일 낮은 吾羅牧場에서 組蛋白質 含量이 낮았다. 4. 本 野草地에 分包된 全植生中 잔디가 56.61%로서 가장 높았으며 그 다음은 고사리 16.44%, 억새 3.76% 순위였다. 科別로는 禾本科가 72.08%. 登科 1.81% 고사리과 16.49%, 기타 9.62%였다. 5. 1일 增體率이 높은 河源牧場은 禾本科와 登科의 比率이 높았고 增體率이 낮은 吾羅와 龍崗牧場은 독생이 있는 고사리 比率이 높은 것으로 나타났다.

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Isolation of Azukisaponin V Possessing Leucocyte Migration Inhibitory Activity from Melilotus officinalis

  • Kang, Sam-Sik;Lee, Young-Soon;Lee, Eun-Bang
    • 생약학회지
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    • 제18권2호
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    • pp.89-93
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    • 1987
  • Chemical investigation of the inhibitory compound on leucocyte migration from Melilotus officinalis has led to the isolation and characterization of azukisaponin V $(3-O-[{\alpha}-L-rhamonopyranosyl(1{\rightarrow}2)-{\beta}-D-glucopyransosyl(1{\rightarrow}2)-{\beta}-D-glucuronopyranosyl]-soyasapogenol B)$ as the carboxylate form, which exhibits potent leucocyte migration inhibitory activity at a dose of 6mg/rat.

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Anti-inflammatory action of soy isoflavonoid sophoricoside by inhibition on cyclooxygenase-2 and cytokines

  • Kim, Byung-Hak;Min, Kyung-Rak;Kim, Young-Soo
    • 대한약학회:학술대회논문집
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    • 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.1
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    • pp.212.3-213
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    • 2003
  • Polyphenolic compounds including flavonoids are wide spread in the plant kingdom, and interested recently because epidemiological studies have suggested correlations between the consumption of polyphenol-rich plant foods and the prevention of chronic diseases. Soy is a main source of isoflavonoids which are high dietary intake for the oriental population. In this study, anti-inflammatory action of sophoricoside, an isoflavone glycoside isolated from immature fruits of Sophora japonica (Leguminosae family), has been demonstrated. (omitted)

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Lipid and Protein Constituents of Crotalaria juncea L.

  • Javed, Muhammad Akhtar;Saleem, Muhammad;Yamin, Muhammad;Chaudri, Tanvir Ahmad
    • Natural Product Sciences
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    • 제5권3호
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    • pp.148-150
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    • 1999
  • Seed lipids and proteins of Crotalaria juncea L were analyzed for fatty acids and amino acids respectively. Gas chromatographic analysis of the oil gave palmitic acid (16.01%), stearic acid (7.29%), oleic acid (14.41%), linoleic acid (54.44%) and linolenic acid (7.86%). The defatted seed cake contained all the essential amino acids except methionine and six non-essential amino acids.

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Phenolic Compounds from Caesalpinia sappan and Their Inhibitory Effects on LPS-induced NO Production in RAW264.7 Cells

  • Min, Byung Sun;Cuong, To Dao
    • Natural Product Sciences
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    • 제19권3호
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    • pp.201-205
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    • 2013
  • Thirteen phenolic compounds, 1,4-dimethoxybenzene (1), 3,4-dihydroxybenzaldehyde (2), (2E)-3-(4-hydroxy-3,5-dimethoxyphenyl)acrylaldehyde (3), 3,7-dihydroxy-4H-chromen-4-one (4), 2,3-dihydroxy-1-(3,4-dihydroxyphenyl)propan-1-one (5), 4-hydroxy-3-methoxybenzoic acid (6), 4-hydroxy-3,5-dimethoxybenzoic acid (7), methyl 3,4-dihydroxybenzoate (8), 4-hydroxy-3,5-dimethoxybenzaldehyde (9), 3,4-dihydroxybenzoic acid (10), 3-hydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-1-one (11), 2,4,6-trihydroxybenzaldehyde (12) and benzene-1,2,4-triol (13) were isolated from the heartwood of Caesalpinia sappan. Their anti-inflammatory activity was evaluated against LPS-induced NO production in macrophage RAW264.7 cells. Among them, compounds 3 and 8 showed strong inhibitory activities toward the LPS-induced NO production in macrophage RAW264.7 cells with $IC_{50}$ values of 14.5 and 21.5 ${\mu}M$, respectively.

계혈등(Mucuna birdwoodiana)의 $3{\alpha}-Hydroxysteroid\;dehydrogenase$억제 성분 (Inhibitory Activities of Three Compounds from Mucuna birdwoodiana on $3{\alpha}-Hydroxysteroid\;dehydrogenase$)

  • 권용수;이진훈;김창민
    • 생약학회지
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    • 제30권2호
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    • pp.216-221
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    • 1999
  • The NAD(P)-linked $3{\alpha}-Hydroxysteroid$ $dehydrogenase(3{\alpha}-HSD)$ of rat liver cytosol is powerfully inhibited by the non-steroidal anti-inflammatory drugs in rank-order of their therapeutic potency, and this observation has now been developed into a rapid screen for predicting the potency of products that show anti-inflammatory effect. Five-plants were screened by using this method. Among them, BuOH-fraction of Mucuna birdwoodiana showed strong inhibitory effect on $3{\alpha}-HSD$, and three isoflavone compounds were isolated. Inhibitory activates of isolated compounds were compared.

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잔디밭 잡초의 분류학적 특성에 관한 연구 (Studies on the Classification Chracteristic of Lawn Weeds)

  • 이명선
    • 아시안잔디학회지
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    • 제2권1호
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    • pp.59-64
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    • 1988
  • This study was carried out to investigate the classification and the growing charicteristics of weed species in a newly formed lawngrass land. The results obtained are summarized as follows: 1)Weed population in a newly formed lawn field consisted of 30% of Gramineae, 15% of Compositae, and 12% of Leguminosae family. 2)Percentage of weed emergence between April and May was 39.4%. The same amount of weed emergence was observed at the period of September and October, where as the percentage was 21.2% at the period of March and April. 3)The population ratio of flowering date of weed species was in order of 48.5% July and August, 30.3% in May and July, 12.1% in March and April, and 9.1% in September and October. 4)Weed classification by life cycle showed 39.4% of biennials, 33.3% of annuals, and 27.3% of perennials. 5)Weed species were grouped according to the plant height. The ratios of each group were 33.3% of 20~40cm group, 27.3% of 40~60cm group, 24.2% of shorter than 20cm group, and 15.2% of taller than 60cm group.

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Phenolic Compounds from Desmodium caudatum

  • Li, Wei;Sun, Ya Nan;Yan, Xi Tao;Yang, Seo Young;Choi, Chun Whan;Kim, Young Ho
    • Natural Product Sciences
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    • 제19권3호
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    • pp.215-220
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    • 2013
  • Three C-glucosyl flavones (1 - 3), one xanthone (4), and four flavanonols (5 - 8) were isolated by various chromatographic methods from the leaves and stems of Desmodium caudatum (Thunb.) DC. Chemical structures of these compounds were elucidated by 1D and 2D NMR and mass spectroscopy. The compounds were identified as swertisin (1), spinosin (2), 7-methyl-apigenin-6-C-${\beta}$-glucopyranosyl-2"-O-${\beta}$-D-xylopyranoside (3), 1,3,5,6-tetrahydroxyxanthone (4), yokovanol (5), aromadendrin (6), 2'-hydroxy yokovanol (7), and 2'-hydroxy neophellamuretin (8). Compounds 2 - 4 were first isolated from D. caudatum, as well as the spectroscopic data for compound 3.