• Natural Product Sciences
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• 제14권1호
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• pp.56-61
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• 2008

Bioactivity guided phytochemical study of the petroleum ether and butanol extracts of Clematis hirsuta resulted in the isolation of 12 compounds. Rat paw edema as a model of acute inflammation was used to evaluate the anti-inflammatory activity of the extracts and the chromatographic fractions. Five known sterols and triterpenes namely: ${\beta}-amyrin$ (1), lupeol (2), ${\beta}-sitosterol$ (3), oleanolic acid (4) and stigmasterol glycoside (5) were isolated from the petroleum ether extract. The n-butanol extract afforded two compounds reported for the first time from natural source: (S)-(+)-dihydro-5-(hydroxymethyl)-2(3H)-furanone (7) and (s)-(-)-5-hydroxymethyl-2(5H)-furanone (8). In addition, anemonin (6), dihydro-4-hydroxy-5-(hydroxymethyl)-2(3H)-furanone (2-deoxy-D-ribono-1,4-lactone) (9), biophenol (cimidahurin) (10), glucose (11) and sucrose (12) were also identified. The structures were determined from spectroscopic data including 1D- and 2D-NMR experiments.

• 생약학회지
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• 제9권2호
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• pp.57-72
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• 1978

The constituents of Ranunculaceae plants are summerized from more than one hundred of papers. Fifteen steroidal alkaloids, thirty two of terpenoids (diterpenes and triterpenes), fifty four isoquinoline alkaloids are recorded. Thirty three papaverines, eighteen berberines, and three hydrastines belong to isoquinoline group. Besides, of alkaloids a number of glycosides are also found. Adonis glycoside, famous cardiotonics, from Adonis and cyanogenin glycoside and calthoside D were identified from the leaves of Thalictrum aquilegifolium and Caltha silvestris. Anemonin, the irritating substance, found in Pulsatilla grandiz $W_{ENDER}$. Kaempf-erol and dihydrokaempferol were isolated and identified from the leaves of Clematis brachyura ^M_{AXIMOWICZ}$ by author in 1968.

• 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.343.2-343.2
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• 2002

Ranunculin (RAN). isolated from Ranunculaceae. exhibited significant cytotoxic activity against KB and Bel-7402 cells with ED$_{50}$ values of 0.21 and 0.35).${\mu}4M respectively. Under physiological condition. the ranunculin was deglycosylated to be protoanemonin. an active form containing ${\alpha}{\beta}$-unsaturated ketone moiety. which successively dimerized to be anemonin inactive form. (omitted)

• 농약과학회지
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• 제7권4호
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• pp.248-257
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• 2003

본 연구의 목적은 국내의 자생식물 중 살초활성이 있는 식물 종을 선발하는데 있다. 국내의 자생식물 73과(科) 200종(種) 시료로부터 MeOH 조추출물을 얻은 다음 24-well plate에서 유채 (Brassica napus L.) 에 대한 살초효과를 검정하였다. 실험에 사용한 200종 식물 중 6종 식물 - 고추나무 (Staphylea bumalda), 등나무(Wistaria floribunda), 산마늘(Allium victorialis), 소리쟁이(Rumex crispus), 이팝나무(Chionanthus retusa), 참느릅 나무 (Ulmus parvifolia)는 높은 살초활성을 나타내었고 ($GR_{50}$ 값, < $1,000{\mu}g\;g^{-1}$), 17종 식물 - 갈퀴덩굴(Galium spurium), 느티나무(Zelkova serrata), 능소화(Campsis gradiflora), 두충(Eucommia ulmoides), 마가목(Sorbus commixta.), 물참대(Deutzia glabrata), 박태기나무(Cercis chinensis), 산오리(Alnus hirsuta), 산초나무(Zanthoxylum schinifolium), 상수리나무(Quercus acutissima), 아까시나무(Robinia pseudoacacia), 주엽나무(Gleditsia japonica), 죽단화(Kerria japonica), 쥐똥나무(Ligustrum obtusifolium), 측백나무(Thuja orientalis), 편백(Chamaecyparis obtusa), 할미꽃(Pulsatilla koreana)은 중정도의 살초활성을 나타내었으나($GR_{50}$ 값, $1,000-2,000{\mu}g\;g^{-1}$), 나머지 177종 식물은 살초활성을 나타내지 않았다. 높은 살초활성을 나타낸 식물로부터 분리되는 천연활성물질들은 향후 새로운 제초제 개발을 위한 모화합물 제공, 상호대립억제 작용성을 갖는 작물 품종 개발 혹은 개량에의 활용, 그리고 친환경 유기농업용 잡초방제에의 활용이 기대된다.