• 제목/요약/키워드: Albizzia julibrissin bark

검색결과 11건 처리시간 0.028초

Sapogenins from albizzia julibrissin

  • Kang, Sam-Sik;Woo, Won-Sick
    • Archives of Pharmacal Research
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    • 제6권1호
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    • pp.25-28
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    • 1983
  • From the stem bark of Albizzia julibrissin (Leguminosae) two known sapogenins, acacigenin B, and machaerinic acid lactone, were isolated and identified by chemical and spectral data. It is the second time that the former was isolate dform the plant sources.

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자귀나무 뿌리껍질의 식물화학적 성분연구 (Phytochemical Constituents of the Root Bark from Albizzia julibrissin Durazz)

  • 고재종;우은란;문영희
    • 생약학회지
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    • 제35권3호통권138호
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    • pp.194-198
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    • 2004
  • Repeated column chromatography of an ethyl acetate extract of the root bark of Albizzia julibrissin Durazz afforded four compounds, euscaphic acid ester glucoside (1), luteolin-7 -O-neohesperidoside (2), (+)-medioresinol (3), (-)-syringaresinol (4). Their structures were determined by chemical and spectroscopic methods. Compounds 1-4 were isolated from this plant for the first time. Among these compounds, (+)-medioresinol (3) exhibited moderate cytotoxic activity against XF 498 and HCT 15 cell line.

A new 4-hydroxy-dodec- 2E-enedioic acid from the stem bark of Albizzia julibrissin

  • Jung, Mee-Jung;Woo, Ju-Jung;Jung, Hyun-Ah;Kang, Sam-Sik;Choi, Jae-Sue
    • 대한약학회:학술대회논문집
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    • 대한약학회 2002년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2
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    • pp.369.3-369.3
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    • 2002
  • Albizzia julibrissin Durazz (Leguminosae) is a small domed to flat-topped, spreading tree with smooth. gray-brown bark and doubly pinnate leaves. It grows abundantly in Korea. The dried stem bark of A. julibrissin is used as a tonic in China, Japan and Korea. From the stem bark of A. ju/ibrissin, a new unsaturated hydroxy fatty acid was isolated and characterized as 4-hydroxy-dodec-2E-enedioic acid on the basis of several data including 2D-NMR. (omitted)

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Anxiolytic-like effects of extracts from Albizzia julibrissin bark in the elevated plus- maze in rats

  • Ahn, Nam-Yoon;Jung, Ji-Wook;Oh, Hye-Rim;Lee, Bo-Kyung;Oh, Jin-Kyung;Cheng, Jae-Hoon;Ryu, Jong-Hoon
    • 대한약학회:학술대회논문집
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    • 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2-2
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    • pp.212.1-212.1
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    • 2003
  • The purpose of the this study was to characterize the putative anxiolytic-like effects of the aqueous extract of Albizzia julibrissin stem bark using the elevated plus maze (EPM) in rats. The water extract of Albizzia julibrissin was orally administered at 10, 50, 100 or 200 mg/kg to adult male SD rats, 1 h before behavioral evaluation in an EPM, respectively. Control rats were treated with an equal volume of saline, and positive control rats buspirone (1 mg/kg). Single or repeated treatment (for 7 days) of the water extract of Albizzia julibrissin (at 100 or 200 mg/kg) significantly increased time-spent and arm entries into the open arms of the EPM, and decreased time-spent and arm entries in the closed arms of the EPM versus saline controls (P < 0.05). (omitted)

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A New (E)-4-Hydroxy-dodec-2-enedioic Acid from the Stem Bark of Albizzia julibrissin

  • Jung, Mee-Jung;Kang, Sam-Sik;Choi, Jae-Sue
    • Archives of Pharmacal Research
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    • 제26권3호
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    • pp.207-209
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    • 2003
  • A new unsaturated hydroxy acid was isolated from the stem bark extract of Albizzia julibrissin through repeated silica gel and Sephadex LH-20 column chromatography. The chemical structure of the new acid was determined as (E)-4-hydroxy-dodec-2-enedioic acid on the basis of several spectral data including 2D-NMR. The stereochemical feature of the double bond was determined to be E on the basis of the coupling pattern of related proton signals in the $^1H-NMR$ and COSY experiments.

Antioxidant Activity from the Stem Bark of Albizzia julibrissin

  • Jung, Mee-Jung;Chung, Hae-Young;Kang, Sam-Sik;Choi, Jin-Ho;Bae, Kae-sun;Choi, Jae-Sue
    • Archives of Pharmacal Research
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    • 제26권6호
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    • pp.458-462
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    • 2003
  • The antioxidant activity of the stem bark from Albizzia julibrissin was evaluated for its potential to scavenge 1,1-diphenyl-2-picrylhydrazyl (DPPH) radicals, to inhibit the generation of the hydroxyl radical ($\cdot OH$), total reactive oxygen species (ROS) and to scavenge authentic peroxynitrites ($ONOO^{-}$). The methanol extract of A. julibrissin exhibited strong antioxidant activity in the tested model systems. Therefore, it was further fractionated using several solvents. The antioxidant activity of the individual fractions were in the order of ethyl acetate (EtOAc) > n-butanol (n-BuOH) > dichloromethane ($CH_2 CI-2$) > and water ($H_2O$). The ethyl acetate soluble fraction, which exhibited strong antioxidant activity, was further purified by repeated silicagel, Sephadex LH-20 and RP-18 gel column chromatography. Sulfuretin (1) and 3 ,4 ,7-trihydroxyflavone (2) were isolated as the active principles. Compounds 1 and 2 exhibited good activity in all tested model systems. Compound 1 exhibited five times more inhibitory activity on the total ROS than Trolox. Compound 2 showed six times stronger DPPH radical scavenging activity than L-ascorbic acid. These results show the possible antioxidant activity of the A. julibrissin crude extract and its major constituents.

자귀나무 추출물이 송사리(Oryzias latipes) 생식소 성숙에 대한 억제효과 (Inhibitory Effects of Extracts from Albizzia julibrissin on Gonadal Maturation in a Medaka (Oryzias latipes))

  • 이은희;오상필;김명희;김광현;홍상훈;한창희
    • 생명과학회지
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    • 제23권3호
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    • pp.333-340
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    • 2013
  • 사료에 첨가된 saponin이 함유된 자귀나무(Albizzia julibrissin) 껍질 추출물이 송사리(Oryzias latipes)의 생식소 성숙과 산란에 미치는 영향을 조사하기 위하여 자귀나무(A. julibrissin) 껍질의 n-BuOH 추출물로부터 Diaion HP-20, Silica gel과 Sephadex LH-20 chromatography들을 이용하여 조 사포닌 분획물(HaBC)을 분리하였다. 실험 어류들은 순환여과 장치 시스템의 수조에서 사육하였으며, HaBC를 첨가한 사료를 급여하여 암컷의 생식소 성숙 억제 및 산란 억제 효과를 조사하였다. 미성숙 송사리들에 대한 실험에서 사료에 HaBC를 20 mg/g-feed 이상 첨가한 사료를 먹인 어류들은 생식소의 성숙과 산란을 개시하는 시기가 지연되었다. 또한 성숙한 암컷 송사리들도 HaBC를 20 mg/g-feed 이상 첨가한 사료를 먹었을 때 대조구에 비해 낮은 GSI 값을 보였다. 미성숙한 송사리에 대한 길이 성장이나 체중에 대한 변화는 HaBC의 첨가량에 관계가 없었으나, 비만도(CF)에서는 HaBC를 첨가한 사료를 먹인 어류들이 대조구에 비해 높은 값을 보였다. 이러한 결과로 자귀나무(A. julibrissin)의 껍질로부터 분리한 saponin 분획물은 송사리 암컷의 성숙을 억제할 수 있었지만, 성장 촉진에는 아무런 작용을 하지 않았다. 이들 작용 기전에 대해서는 더 많은 연구들이 있어야 할 것이다.

Flavonoids from the stem bark of Albizzia julibrissin

  • Jung, Jung-Mee;Yoon, Na-Young;Jung, Hee-Jin;Kang, Sam-Sik;Choi, Jae-Sue
    • 대한약학회:학술대회논문집
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    • 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2-2
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    • pp.197.3-197.3
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    • 2003
  • From the EtOAc fraction of the MeOH extract of Albizzia julibrissin (Leguminosae), a rare 5-deoxy flavone (geraldone), a 3',4',7,8-tetrahydroxyflavanone, an isoflavone (daidzein), and five prenylated flavonoids (sophoflavescenol, kurarinone, kurarinol, kuraridin and kuraridinol) were isolated and identified based on the analysis of spectral data.(omitted)

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Isolation of Flavonoids and a Cerebroside from the Stem Bark of Albizzia julibrissin

  • Jung, Mee-Jung;Kang, Sam-Sik;Jung, Hyun-Ah;Kim, Goon-Ja;Choi, Jae-Sue
    • Archives of Pharmacal Research
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    • 제27권6호
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    • pp.593-599
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    • 2004
  • From the EtOAc fraction of the MeOH extract of Albizzia julibrissin (Leguminosae), a rare 5-deoxyflavone (geraldone, 1), isookanin (2), luteolin (3), an isoflavone (daidzein, 4), five prenylated flavonoids [soph6f1avescenol (5), kurarinone (6), kurarinol (7), kuraridin (8) and kuraridinol (9)], a cerebroside (soya-cerebroside I, 10), and $(-)-syringaresinol-4-O-{\beta}-D-glucopyranoside$ (11) were isolated and characterized on the basis of spectral data. Compounds 2, 3, and 11, showed 1, 1-diphenyl-2-picrylhydrazyl radical scavenging activity.

Inhibitory Effects of the Stem Bark of Albizia julibrissin on Catecholamine Biosynthesis in PC12 Cells

  • Lee, Myung-Koo
    • 생약학회지
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    • 제27권2호
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    • pp.155-158
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    • 1996
  • The methanol extract of Albizzia julibrissin Durazz. (Leguminosae) was successively partitioned into dichloromethane, ethylacetate, butanol (BuOH) and water fractions, and the effects of the each solvent extract on catecholamine biosynthesis in PC12 cells were investigated. Among them, the BuOH fraction $(5{\mu}g/ml\;medium)$ showed 68.8% and 63.6% inhibition on dopamine and norepinephrine content in PC12 cells, respectively. Tyrosine hydroxylase (TH) activity was also reduced markedly by treatment of the BuOH fraction (41.8% inhibition at $5{\mu}g/ml$ in the medium). Each solvent fraction did not show cytotoxicity towards PC12 cells by trypan blue exclusion test. This result suggests that the BuOH fraction has an inhibitory effect on catecholamine biosynthesis by reducing TH activity in PC12 cells.

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