• 제목/요약/키워드: syringin

검색결과 26건 처리시간 0.026초

진피로부터 정제한 Syringin의 항산화 및 항균 활성 (The Anti-oxidant and Anti-microbial Activities of Purified Syringin from Cortex Fraxini)

  • 설민경;배은영;조영제;박순기;김병오
    • 생명과학회지
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    • 제30권8호
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    • pp.695-700
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    • 2020
  • 본 연구에서는 물푸레나무 껍질인 진피로부터 Syringin을 효과적으로 분리, 정제하고 항산화 및 항균 활성을 평가하여 기능성 소재로써의 가능성을 탐구하고자 하였다. Syringin은 DPPH radical 소거활성 평가에서 50 ㎍/ml의 적은 농도로도 BHT보다 높은 활성을 나타내었으며 ABTS radical 소거활성 평가에서는 모든 농도에서 BHT의 활성과 비슷한 정도의 활성을 나타냈다. PF 측정에서는 Syringin의 농도가 증가함에 따라 활성이 다소 높아지는 듯했으나 증가폭이 크지 않았고 모든 농도에서 1.2 PF 이상의 활성이 나타나 항산화력이 있다고 판단하였다. TBARs 활성 측정에서는 모든 농도에서 BHT의 활성보다 낮지만 농도 의존적으로 항산화력이 증가하는 것을 확인할 수 있었다. 그람양성, 그람음성, 진균에 대한 생육 억제 활성 평가에서는 L. monocytogenes KCTC 13064, S. aureus KCTC 1916, E. coli KCTC 2571, H. pylori HPKCTC B0150의 네 균주에 대한 생육억제환의 크기가 Syringin의 농도에 의존적으로 증가하였고 C. albicans ATCC 10231에 대해서는 생육억제환이 관찰되지 않았다. 위의 결과를 종합한 결과 Syringin의 수용성 물질의 항산화 활성은 지용성 물질의 항산화 활성보다 우수하고 진균을 제외한 그람양성 및 그람음성 균주에 대한 성장을 억제함으로써 항균 활성을 나타낸다고 판단하였다. 본 연구를 토대로 Syringin의 항산화 및 항세균 기작에 대한 연구와 다른 생리활성 작용, 인체 적용성에 대한 연구를 추가로 진행한다면 천연 유래의 안전한 기능성 소재로 활용 가능할 것으로 사료된다.

Isolation of Triterpenoid and Phenylpropanoid from Codonopsis ussuriensis

  • Lee, Ihn-Rhan;Ko, Jeong-Hyun
    • Archives of Pharmacal Research
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    • 제15권4호
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    • pp.289-291
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    • 1992
  • From the roots of Codonopsis ussuriensis (Rupr. et Maxim) Hemsley (Campanulaceae), taraxerol (mp 280-$282^\circ$), syringin (mp.$192^\circ$) and a new phenylpropanoid, ussurienoside I (syringin-3'-hydroxy-3'-methyl glutarate, mp. 102-$104^\circ$) were isolated.

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Metabolism of Liriodendrin and Syringin by Human Intestinal Bacteria and their Rlation to in Vitro Cytootoxicity

  • Kim, Dong-Hyun;Lee, Kyung-Tae;Bae, Eun-Ah;Han, Myung-Joo;Park, Hee-Juhn
    • Archives of Pharmacal Research
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    • 제22권1호
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    • pp.30-34
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    • 1999
  • When liriodendrin or syringin was incubated for 24 h with human intestinal bacteria, two metabolites, (+)-syringaresinol$\beta$--D-glucopyranoside and (+)-syringaresionl, from liriodendrin and one metabolite, synapyl alcohol, from syringin were produced. The metabolic time course of liriodendrin was as follows: at early time liriodendrin was converted to (+)-syringaresinol-$\beta$-D-glucopyranoside, and then (+)-syringaresinol. The in vitro cytotoxicities of these metabolites, (+)-syringaresinol and synapyl alcohol, were superior to those of liriodendrin and syringin.

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HPLC 분석에 의한 해동피와 개두릅의 성분함량 비교 (Quantitative Determination on the Constituents of the Stem Bark and the Leaf Shoot of Kalopanax pictus by HPLC Analysis)

  • 김민영;유영민;남정환;최종원;박희준
    • 생약학회지
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    • 제38권3호통권150호
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    • pp.270-276
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    • 2007
  • To evaluate the leaf shoots and stem barks of Kalopanax pictus (Araliaceae) as an edible vegetable and a traditional medicinal drug, respectively, the compounds of syringin, liriodendrin, astragalin, quercetin, and kalopanaxsaponins were quantitatively measured by HPLC analysis. The leaf shoot exhibited low contents of syringin, liriodendrin and kalopanaxsaponins but a high chlorogenic acid content, whereas the grown leaves contained very high amounts of kalopananxsaponins. In contrast, the stem bark had very high amounts of syringin and liriodendrin and relatively low kalopanaxsaponins. In particular, the kalopanaxsaponin contents were rapidly increased with monthly variation until October but decreased from September. It was also observed that the leaf shoot contained chlorogenic acid by 30.73 mg/g and the barks showed the concentration of liriodendrin by 20.75 mg/g. These results indicate that high contents of syringin and liriodendrin in the stem bark and high contents of chlorogenic acid in the leaf shoot support scientific bases on the traditional uses of K. pictus as a medicinal drug and a functional food, respectively.

함박꽃나무(Magnolia sieboldii)의 추출성분 (Extractives from Magnolia siebildii)

  • 최인호;이학주;최돈하;박재인;최태호
    • Journal of the Korean Wood Science and Technology
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    • 제32권2호
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    • pp.33-39
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    • 2004
  • 함박꽃나무 수피 및 목부의 EtOH 조추출물로부터 prep. TLC, silica gel 및 Sephadex LH-20 칼럼 크로마토그라피를 이용하여 4종의 화합물을 단리하였다. 이들 화합물들은 NMR, MS 등의 기기분석에 의해 sesquiterpene lactone 구조의 costunolide (I)를 비롯하여, 리그난 배당체 화합물인 syringin (II)과 1, 2-dihydroxyxanthone (III) 및 vanillic acid (IV)으로 각각 동정하였다.

함박꽃나무 잎으로 부터 새로운 Aporphine계 Alkaloid 성분의 분리 (A New Aporphin-Type Alkaloid from the Leaves of Magnolia sieboldii K. Koch)

  • 박희준
    • 생약학회지
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    • 제27권2호
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    • pp.123-128
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    • 1996
  • From the leaves of Magnolia sieboldii a new aporphine-type alkaloid named magnoporphine was isolated. The structure of magnoporphine was all assigned by $^1H-^1H$COSY, $^1H-^{13}C$ COSY and $^1H-^{13}C$ long range NMR. In addition, costunolide, syringin, syringenin $4-O-{\beta}-cellobioside$ and echinacoside was isolated.

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Anti-Platelet Effect of the Constituents Isolated from the Barks and Fruits of Magnolia obovata

  • Pyo, Mi-Kyung;Lee, Yong-Yook;Yunchoi, Hye-Sook
    • Archives of Pharmacal Research
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    • 제25권3호
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    • pp.325-328
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    • 2002
  • In the course of our work on anti-platelet constituents from plants, five phenolic compounds, magnolol, honokiol, obovatol, methyl caffeate, and syringin, were isolated from the methanol extracts of the barks and fruits of Magnolia obovata. The compounds were identified based on the spectroscopic data. Methyl caffeate was isolated for the first time from the genus Magnolia and it showed 3∼4-folds higher potency than ASA. The activities of obovatol and honokiol were comparable to ASA. Magnolol and syringin showed only very mild inhibitory effects to all the stimulators.

Studies on the Constituents of the Stem Barks of Acanthopanax gracilistylus W. W. Smith

  • Liu, Xiang Qian;Chang, Seung-Yeup;Park, Sang-Yong;Nohara, Toshihiro;Yook, Chang-Soo
    • Natural Product Sciences
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    • 제8권1호
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    • pp.23-25
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    • 2002
  • Ten compounds were isolated from the stem barks of Acanthopanax gracilistylus WW Smith (AGS) by steam distillation, they were p-menta-1,5,8-triene, n-butyl isobutylphthalate, p-mentha-1,5-diene-8-ol, 8-hydroxy-p-cymene, myrtenol, trans-(+)-carveol, 1,3-di-tert-butylbenzene, 4-methyl-2,6-di-butylphenol, valencene and verbenone, respectively, characterized by GS-Mass spectra. And we have also extracted and isolated from the MeOH extracts of the stem barks of AGS, two compounds were obtained. On the basis of chemical and spectral evidence, they were syringin(l), ${\beta}-sitosterol(2)$.

Phytochemical Constituents of Acanthopanax senticosus (Rupr. & Maxim.) Harms Stem

  • Ryu, Ji-Young;Son, Dong-Wook;Kang, Jung-Il;Lee, Sang-Yun;Kim, Hyun-Su;Shin, Kuk-Hyun;Lee, Sang-Hyun
    • 한국약용작물학회지
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    • 제11권4호
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    • pp.306-310
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    • 2003
  • Five constituents were isolated from the stem of Acanthopanax senticosus. Their structures were elucidated as (-)-sesamin (1), iso-fraxidin (2), 5-hydroxymethylfurfural (3), syringin (4) and acanthoside D (5) by spectral analysis. Among these compounds, 5-hydroxymethylfurfural (3) was isolated for the first time from this plant.

상기생의 트라이테르펜 및 페놀성 성분 (Triterpenes and Phenolic Constituents from Viscum album L.)

  • 최상진;권학철;정애경;최상운;김경란;이선미;표석능;이강노
    • 약학회지
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    • 제45권6호
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    • pp.591-598
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    • 2001
  • The photochemical study of Viscum album (Loranthaceae) led to the isolation of twelve compounds, lupeol (1), betulonic acid (2), betulinic acid (3), terminic acid (4), ursolic acid (5), $\beta$-sitosterol (6), $\alpha$- spinasterol (7), oleanolic acid (8) , 5-hydroxy-1- (4′-hydoxyphenyl) -7- (4"-hydroxyphenyl) -hepta-1- en-3-on (9), 2′-hydroxy -4′, 6′- dimethoxychalcone -4-O-glycoside (10) ,2′-hydroxy-4′, 6′-dimethoxychalcone -4-O- [apiosal(1longrightarrow12)]glucoside (11) and syringin (12). Their structures were established by chemical and spectroscopic methods. The cytotoxicity of the isolated compounds was evaluated by sulforhodamine B assay against five cultured human tumor cell lines.

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