• 제목/요약/키워드: triterpene glycosides

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병풀 잎에서 triterpene glycosides의 시기별 함량변화 (Seasonal variations of triterpene glycosides contents in the leaf of Centella asiatica (L.) Urban)

  • 김옥태;김민영;김수정;김유정;김광수;안준철;김시욱;황백
    • 한국약용작물학회지
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    • 제10권5호
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    • pp.375-378
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    • 2002
  • 5월부터 10월까지 병풀의 지상부에 triterpene glycosides인 madecassoside와 asiaticoside의 시기별 함량변화를 조사하였다. 잎에서는 9월에 약 108.1 mg/g으로 가장 높은 수준의 함량을 보였다. 엽병에서는 19.02 mg/g으로 잎에서 보이는 수준보다는 낮은 수준을 나타냈다. 병풀의 triterpene glycosides는 잎에 주로 축적되며, 가장 적절한 병풀의 수확시기는 9월로 잠적 확인되었다.

Synthesis of $^3H$-Labeled dammarane triterpene glycosides of Korean ginseng

  • Han, Byung-Hoon;Woo, Lin-Keun
    • Archives of Pharmacal Research
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    • 제1권1호
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    • pp.27-32
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    • 1978
  • A procedure of $^3H$-radio labeling synthesis for the dammarane triterpene glycosides of Korean ginseng was established by using the ginsenoside $Rg_1$ as starting material. The protons in $C-{11}$ and $C_{13}$ of the aglycone moiety of the glycoside were exchanged with tritium by keto-enol tautomerization of 12-keto-ginsenoside $Rg_1$ which was prepared by partial acetylation, Sarett oxidation and saponification, producing nona-acetate, nonaside $Rg_1$. The acety1-ketone and 12-keto-derivative of ginsenotritated ketone was reduced by metallic sodium and isoproponol to produce the end product $^3H$-ginsenoside $Rg_1$ with 3% radio-chemical recovery in one experiment.

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A Triterpene Glucosyl Ester from the Roots of Rubus crataesifolius

  • Jung, Sung-Wook;Shin, Myung-Hee;Jung, Jee-H.;Kim, Nam-Deuk;Im, Kwang-Sik
    • Archives of Pharmacal Research
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    • 제24권5호
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    • pp.412-415
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    • 2001
  • Along with five known triterpene glycosides, a new triterpene glucosyl ester, named crataegioside, was isolated from the roots of Rubus crataesifolius Bunge. The structure was established as ilexosapogenin A 28-O-$\beta$-D-glucopyranosyl ester by chemical and spectroscopic methods.

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Further Triterpene Glycosides from Echinosophora koreensis

  • Byun, Ji-Hye;Kim, Ju-Sun;Kang, Sam-Sik
    • 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.135.1-135.1
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    • 2003
  • We have previously reported three new oleanene-type glycosides and kudzusaponin $A_3$ methyl ester and subproside II methyl ester from the roots of Echinosophora koreensis. Further study has now led to the isolation of three known oleanen-type glycosides. sophoraflavoside I, azukisaponin V, and kudzusaponin $SA_3$ as their methyl esters. The structures of theses compounds were characterized by spectroscopic and chemical methods.

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병풀 (Centella asiatica L. Urban) 식물체 배양을 이용한 Triterpene Glycoside 생산 (Production of Triterpene Glycosides from Whole Plant Cultures of Centella asiatica (L.) Urban)

  • 김옥태;김민영;박윤정;홍민희;안준철;오만호;황백
    • Journal of Plant Biotechnology
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    • 제29권4호
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    • pp.281-285
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    • 2002
  • 기내에서 병풀의 식물체 배양을 확립하였고 기본배지 설정 및 대량원소들, sucrose 농도가 triterpene glycoside (Made-cassoside와 Asiaticoside: M&A) 생산에 대한 영향을 조사하였다. 병풀 식물체가 각각의 배지에서 배양되었을 때, MS와 RCM배지는 각각 식물체 생장과 M&A 생산에 대해 가장 좋은 결과를 나타냈다. 하지만, M&A에 대해 가장 높은 생산성은 B5 배지로 나타내었다. B5 배지의 대량영양소인 KNO$_3$는 25 mM, NaH$_2$PO$_4$는 1 mM, CaC1$_2$는 1 mM 그리고 MgSO$_4$는 1~10 mM에서 M&A 생산이 최적을 이루거나 증가시켰다. Sucrose를 농도별로 처리했을 때, 6% sucrose 농도에서 가장 높은 M&A 생산을 얻을 수 있었다.

A New Lupane-Triterpene Glycoside from the Leaves of Acanthopanax gracilistylus

  • Liu, Xiang-Qian;Chang, Seung-Yeup;Park, Sang-Yong;Nohara, Toshihiro;Yook, Chang-Soo
    • Archives of Pharmacal Research
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    • 제25권6호
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    • pp.831-836
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    • 2002
  • A new and two known lupane-triterpene glycosides were isolated from the hot MeOH fraction of the leaves of Acanthopanax gracilistylus W. W. Smith. Based on the physical properties and spectroscopic data, their chemical structures were determined as acankoreoside A (1), acankoreoside D (2), and $3{\alpha}-hydroxy-lup-23-al-20(29)-en-28-oic$ acid $28-O-{\alpha}-L-rhamnopyranosyl-(1{\rightarrow}4)-{$beta}-D-glucopyranosyl-(1{\rightarrow}6)-{\beta}-D-glucopyranosyl$ ester (3), respectively. To our best knowledge, compand 3 appears to be novel, which was named as wujiapioside A.