• 제목/요약/키워드: Diterpene

검색결과 83건 처리시간 0.021초

생강나무 잎과 가지의 정유성분 (Essential Oils from Leaves and Twigs of Lindera obtusiloba)

  • 권동주;김진규;배영수
    • 한국산림과학회지
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    • 제96권1호
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    • pp.65-69
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    • 2007
  • 생강나무(Lindera obtusiloba Blume) 잎과 가지의 정유성분을 수증기 증류법으로 분리하고 GC-MS로 NIST와 Wiley 6 Library 스펙트럼과 비교하여 구성성분을 분석하였다. 생강나무 잎과 가지에서 총 24개의 성분을 동정하였으며 sesquiterpene 화합물들이 주요 구성성분이었다. 생강나무 잎에서 분리한 정유의 주요 구성성분은 germacrene B(17.78%), ${\beta}-caryophyllene$(17.50%), phytol isomaer(13.36%), $(-)-{\beta}-elemene$(11.07%) 등이었고, 가지에서는 ${\beta}-elemol$(24.47%), ${\alpha}-cadinol$(13.73%), camphor(9.83%) and ${\beta}-citronellol$ (9.54%) 등이 주요 구성성분이었다. Acyclic diterpene인 phytone, phytol 및 phytol isomer 등의 화합물들은 생강나무 잎에서 처음 분석되었다.

Salvatrione: A Diterpene-monoterpene Conjugate from Salvia bucharica

  • Ahmad, Viqar Uddin;Zahid, Muhammad;Ali, Muhammad Shaiq;Jassbi, Amir Reza;Ahmad, Shakeel;Ali, Zulfiqar;Iqbal, Muhammad Zafar
    • Natural Product Sciences
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    • 제6권2호
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    • pp.66-69
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    • 2000
  • Salvia bucharica belonging to the family Lamiaceae (Labiatae), afforded a novel terpenoid (1) named as salvatrione. The structure of 1 was elucidated through extensive 2-D NMR experiments and the biogenetic pathway of 1 has also been proposed. On biogenetic grounds, 1 may be considered to be a pseudo-triterpenoid as it is derived from the coupling of mono/ diterpenic units and not from squalene.

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희첨의 새로운 Diterpene 배당체에 관하여 (A New Diterpenic Glucoside of Siegesbeckia pubescens)

  • 김제훈
    • 생약학회지
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    • 제3권1호
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    • pp.21-22
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    • 1972
  • 우리 나라 한방요법(漢方療法)에서 고혈압치료(高血壓治療)에 널리 쓰이고 있는 희염은 털진득찰 Siegesbeckia pubescens의 전초(全草)로서 그 유효성분(有成分)으로서는 이미 물질(物質) $A\;C_{20}H_{34}O_4\;mp\;192{\sim}193^{\circ}\;[{\alpha}]^{20}_D\;-22\;(in\;dioxane),\;B\;C_{20}H_{32}O_4\;260.2^{\circ}[{\alpha}]^{20}_D\;-88\;(in{\;}pyridine)$의 화학구조(化學構造) 및 생리작용(生理作用)을 밝힌 바 있다. 본 연구에서는 또하나의 새로운 배당체(配糖體) $compound(I)\;C_{26}H_{44}O_8\;mp\;225{\sim}6^{\circ}[{\alpha}]^{20}_D\;-40$을 얻어 그의 이화학적(理化學的) 성상(性狀) 및 유도체(誘導體)의 합성(合成)으로서 화학구조(化學構造)를 구명(究明)하였다.

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Screening and Isolation of Antibiotics Resistance Inhibitors from Herb Materials. V.- Resistance Inhibition by Acorenone from Acorus gramineus Solander

  • Kim, Hye-Kyung;Moon, Kyung-Ho;Lee, Chung-Kyu
    • Natural Product Sciences
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    • 제6권1호
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    • pp.36-39
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    • 2000
  • Acorenone, a diterpene isolated from Acorus gramineus, showed strong resistance inhibitory activity against multi-drug resistant microorganisms such as Staphylococcus aureus SA2, which has resistance to 10 usual antibiotics including chloramphenicol (Cm). At the level of $5\;{\mu}g/ml$ when combined with $50\;{\mu}g/ml$ of Cm. Bacterial resistance to Cm is due to the presence in resistant bacteria of an enzyme, chloramphenicol acetyltransferase (CAT), which catalyses the acetyl-CoA dependent acetylation of the antibiotic at C-3 hydroxyl group. To elucidate the mechanism of resistant inhibitory effect, the acorenone which had the strongest resistant inhibitory activity, was investigated on the CAT assay. As the result, the combination of Cm and acorenone showed the strongest inhibitory activity on CAT as noncompetitive and dose dependent manner.

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초오 성분이 포함된 화풍단 복용 후 발생한 심실 부정맥 2례 (Ventricular Arrhythmia Following Aconitine-Ingestion - 2 Case Reports -)

  • 김미란
    • 대한임상독성학회지
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    • 제4권2호
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    • pp.180-186
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    • 2006
  • The various species of aconitum contain diterpene (C-20) and norditerpene (C-19) forms of the natural alkaloid aconitine that cause neurologic, gastrointestinal, cardiovascular symptoms. In chinese medicine, these plants has been used as drugs to treat pain, dyspepsia, cerebrovascular disease, and so on. Because the therapeutic window is narrow, poisoning may occur from unintentional exposure, with a variety of toxic effects such as arrhythmia, hypotension, paresthesia, paralysis, nausea, vomiting, and abdominal pain. Aconitine-containing folk remedies are widely used in Korea. We encountered two cases of ventricular arrhythmia in patients who ingested tablets, known as 'Wha-Pung-Dan' made with aconitine extracts and were subsequently admitted to the ED. A 42 year-old man who took 35 tablets presented with ventricualr tarchycardia, and 40 year-old woman who took 40 tablets showed premature ventricular contractions. Both patients were discharged normally without any complications after three days.

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글루타메이트에 의한 신경독성에 미치는 징코라이드의 영향 (Ginkgolides Attenuate Glutamate-Induced Neurotoxicity in Primary Cultures of Rat Cortical Cells)

  • 김소라;전미희;김영중
    • 약학회지
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    • 제40권6호
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    • pp.720-726
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    • 1996
  • The neurotoxicity induced by L-glutamate in primary cultures of rat cortical cells could be attenuated by diterpene constituents of Ginkgo biloba leaves, ginkgolides A, B and C. At the concentration of 100 nM, ginkgolides up-regulated the activity of glutathione reductase in primary cultures of rat cortical cells exposed to 100 ${\mu}$M glutamate. Furthermore, ginkgolides increased the content of reduced glutathione in glutamate-treated cortical cells. However, ginkgolides showed little effect in reducing superoxide dismutase activity. Ginkgolides did, however, markedly block the production of malondialdehyde, a byproduct of lipid peroxidation in glutamate-treated rat cortical cells.

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Anti-tumor Activity of Dendrostellera lessertii and the Inhibitory Effect of One of Its Purified Diterpene Ester on Wehi-164 cell Adhesion

  • Yazdanparast, R.;Mianabadi, M.;Abdolmohammadi, M.H.
    • Natural Product Sciences
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    • 제9권3호
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    • pp.161-166
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    • 2003
  • In the course of our studies for new anticancer medicinal plants, we evaluated the effects of an alcohol-water (1:1, V/V) extract of Dendrostellera lesserii (Thymelaeaceae) leaves on the growth rates of breast tumors of rats. The breast tumors were induced in a group of rats by Dimethylbenz[a]anthracene (DMBA) injection. Our data showed that daily oral feeding of the crude extract to the rats, for 20 consecutive weeks, significantly repressed the growth rates of the breast tumors. In addition, the probable effect of D. lessertii crude extract or one of its purified active components on metastasis was evaluated using wehi-164 cells. Treatment of the cells with a single nontoxic dose of the purified active component for 48 hours inhibited the adhesion of the cells to the immobilized fibronectin molecules by almost 80% compared to the untreated control cells.