• 제목/요약/키워드: Triterpene acetate

검색결과 12건 처리시간 0.021초

산씀바귀의 Triterpenoid 성분조성 (Triterpenoid constituents of the Herbs of Lactuca raddeana)

  • 박희준;윤세영;곽태순;최재수;박종희
    • 한국약용작물학회지
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    • 제3권2호
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    • pp.151-155
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    • 1995
  • 국화과 식물인 산씀바귀(Lactuca raddeana)를 식물화학적 방법에 의하여 연구한 바 primaylong chain alcohol인 1-hexacosanol과 1-tetracosa not을, triterpene acetate로 ${\beta}-amyrin\;acetate,\;{\alpha}-amyrin acetate$, lupeol acetate, pseudotaraxasterol acetate, taraxasterol acetate 및 germanicol acetate등을, fatty acyl triterpene은 이들의 구성 triter pone alcohol이 triterpone acetate의 경우와 같았으며 acyl moiety는 myristate, palmitate, stearate및 arachidate로 각각 나타났다.

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왕고들빼기로부터 얻은 Triterpene Acetate의 혈청 콜레스테롤 저하효과 (Serum Cholesterol Lowering Effect of Triterpene Acetate Obtained from Lactuca indica)

  • 김미정;이은;차배천;최무영;임태진;박희준
    • 생약학회지
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    • 제28권1호
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    • pp.21-25
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    • 1997
  • The diets with three types of triterpenoid constituents, which were isolated from Lactuca indica, provoked significant changes of serum lipoprotein-cholesterol meta bolisms of hypercholesterolemic rats induced by high-cholesterol diet, together with the reduction of atherogenic index. Especially, triterpene acetates which have triterpene moieties such as ${\beta}-amyrin$, ${\alpha}-amyrin$, lupeol, pseudotaraxasterol, taraxasterol and germanicol showed a considerable hypocholesterolemic activity. The rat given orally with triterpene acetates did not exhibit a significantly higher value of atherogenic index than that of normal rats.

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뽀리뱅이의 세포독성 트라이테르펜 하이드로퍼옥사이드 성분 (A new Cytotoxic Triterpene Hydroperoxide from the Aerial Part of Youngia japonica)

  • 이강노;이원빈;권학철;이재훈;최상운
    • 약학회지
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    • 제46권1호
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    • pp.1-5
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    • 2002
  • A new cytotoxic triterpene hydroperoxide (3) was isolated from the methylene chloride extract of the aerial part of Youngia japonica together with four known triterpenes (1, 2, 4 and 5). Their structures were identified by means of physico-chemical and spectral data to be $\beta$-amyrin acetate (1), taraxasterol (2), 2l$\alpha$-hydroperoxy-taraxasterol (3), oleanolic acid (4) and ursolic acid (5). Compounds 3 and 5 showed moderate cytotoxicity against five tumor cell lines.

Anti-Complementary Activity of Protostane-Type Triterpenes from Alismatis Rhizoma

  • Lee, Sang-Myung;Kim, Jung-Hee;Zhang, Ying;An, Ren-Bo;Min, Byung-Sun;Joung, Hyouk;Lee, Hyeong-Kyu
    • Archives of Pharmacal Research
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    • 제26권6호
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    • pp.463-465
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    • 2003
  • Four protostane-type triterpenes, alisol B 23-acetate (1a), alisol C 23-acetate (2a), alisol B(3a), and alisol A 24-acetate (4a), were isolated from the rhizome of Alismatis plantago-aquatica L. var. orientale Samuelson (Alismataceae) and eleven protostane derivatives (compounds 1-11) were obtained by selective modification from alisol B 23-acetate (1a). These compounds were investigated for their anti-complement activity against the classical pathway of the complement system. Alisol B (3a) and alisol A 24-acetate (4a) exhibited anti-complement activity with $IC_{50} values of 150 and 130 \mu$ M. Among the synthetic derivatives, the tetrahydroxylated protostane triterpene (9) showed moderate inhibitory activity with $IC_{50} value of 97.1 \mu$ M. Introduction of an aldehyde group at C-23 (10; $IC_{50} value, 47.7 \mu$ M) showed the most potent inhibitory effect on the complement system in vitro.

고들빼기 생리활성물질의 검색 (Exploitation of the biologically active components in Youngia sonchifolia Max)

  • 신수철
    • Applied Biological Chemistry
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    • 제36권2호
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    • pp.134-137
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    • 1993
  • 우리나라 전지역의 산과 들에 야생하고 있는 고들빼기(Youngia sonchifolia Max.)는 전통식품인 고들빼기 김치의 원료로 이용될 뿐만 아니라 오래전부터 민간에서 위장장애 치료재로 이용되어 왔다. 그래서 고들빼기의 생화학적 활성 및 항암 실험과 그 특수성분을 분석하였는데 hexane 추출물 중에서 silica gel column chromatography와 재결정으로 얻어낸 화합물은 무색판상 결정으로 융점이 $280{\sim}282^{\circ}C$ 이었으며 구조결정을 위해 $^{13}C-NMR$, $^1H-NMR$, MS로 분석한 결과 pentacyclic triterpene인 bauerenyl acetate인 것을 확인하였다.

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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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Two New Antiinflammatory Triterpene Saponins from the Egyptian edicinal Food Black Cumin (Seeds of Nigella sativa)

  • Elbandy, Mohamed;Kang, Ok-Hwa;Kwon, Dong-Yeul;Rho, Jung-Rae
    • Bulletin of the Korean Chemical Society
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    • 제30권8호
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    • pp.1811-1816
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    • 2009
  • An extensive phytochemical investigation of the polar fractions of a methanolic extract of Egyptian medicinal food, black cumin (seeds of Nigella sativa L.) led to the isolation of two new triterpene saponins, named sativosides A and B (1-2), along with four known saponins (3-6). Sativoside A (1) is the first example of saponins containing 18-ene triterpene aglycon not only in this Nigella genus but also in the family Ranunculaceae. The structure of the new saponins was elucidated mainly by a combination of 1D and 2D NMR data, together with HRFABMS and acid hydrolysis. Three compounds (1-3) showed the significant inhibition effect of phorbol 12-myristate 13-acetate (PMA) plus calcium ionophore A23187-induced production of IL-6 in a human mast cell (HMC-1) line.

Highly Sweet Compounds from North and South American Medicinal Plants

  • Kinghorn, A.Douglas
    • 생약학회지
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    • 제22권1호
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    • pp.1-12
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    • 1991
  • Nearly 50 highly sweet substances have been isolated and structurally characterized from green plants, and such compounds comprise mainly various types of terpenoids, flavonoids, and proteins. Among the sweet substances that have been studied as constituents of North and South American medicinal plants are the sesquiterpene, hernandulcin, the triterpene glycosides, abrusosides A-D, the steroidal saponins, polypodosides A and B, and the dihydroflavonol, dihydroquercetin-3-acetate. In addition, safety studies have been performed on the potently sweet substance, stevioside, from the 'sweet herb of Paraguay' (Stevia rebaudiana), a compound now produced on a commercial scale.

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Phytochemical Constituents from Saussurea nutans

  • Choi, Sang-Zin;Lee, Sung-Ok;Yang, Min-Cheol;Nam, Jung-Hwan;Lee, Kyu-Ha;Jang, Ki-Uk;Lee, Jong-Hwa;Lee, Kang-Ro
    • 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.198.1-198.1
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    • 2003
  • As part of our systematic study for Korean Compositae plants, we have studied Saussurea nutans, collected at Gangwon Province on August 2001. Phytochemical studies on various species of genus Saussurea have resulted in the isolation sesquiterpene, triterpene and flavonoid$\^$1)/. S. nutans has been used for the treatment of rheumatic arthritis and dysmenorrhea in the Chinese folk medicine$\^$2)/. However, chemical constituents of this plant have not been reported until now. The MeOH extract of the aerial parts of this source was solvent fractionated into n-hexane, methylene chloride, ethyl acetate and BuOH soluble portions. (omitted)

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