• 한국식생활문화학회지
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• 제5권2호
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• pp.243-251
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• 1990

두릅나무 순의 saponin을 추출하여 그 구조를 밝혀 본 결과는 다음과 같다. 1. 자연산 날 것 식용적기의 crude saponin에서 aglycon으로 oleanolic acid와 hederagenin외에 1,3-methylenedioxy-3-dehydroxyoleanolic acid를 동정하였으며 당으로 ${\alpha},\;{\beta}-glucose$와 arabinose, rhamnose를 확인하였다. 2. 자연산 날 것 식용적기에 가장 많은 ‘b’ saponin(elatoside $Fh_2$)을 분리하여 동정한 결과 그 구조는 3-0-$[{\alpha}-L-arabinopyranosyl(1{\rightarrow}2)-{\beta}-D-glucopyranosyl]$-28-O-${\beta}-D-glucopyranosyl$ oleanolic acid라 추정된다.

• 생약학회지
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• 제22권3호
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• pp.162-165
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• 1991

Four triterpenoids were isolated from the leaves and stems of Lycopus lucidus and identified as betulinic acid, oleanolic acid, 3-epimaslinic acid and euscapic acid by spectroscopic methods.

• Archives of Pharmacal Research
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• 제20권3호
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• pp.269-274
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• 1997

Solubilities of oleanolic acid and ursolic acid in aqueous surfactant solutions, liquid polyethylene glycols (PEG), and solvents of various polarity were measured. The results showed that the solutes were slightly or moderately solubilized in the surfactant solutions and the liquid PEGS. It was also revealed that the solutes were slightly soluble in the solvent of either extreme polarity or nonpolarity, but moderately soluble in solvents of intermediate polarity of which solubility parameters are around 10. The solubility parameters of these solutes were calculated from the group contribution to be 10.2 for both of them. Of the solvents tested, tetramethylurea was exceptionally effective in solubilizing the solutes. The solutes were also moderately soluble in the aqueous cosolvents containing tetramethylurea. This suggests that the mixed systems of tetramethylurea could be employed for the solubilization in the formulation of these compounds as an aqueous system.

• 생약학회지
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• 제24권3호
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• pp.247-250
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• 1993

From the Paeoniae Radix, gallic acid methyl ester, (+)-catechin, paconiflorin, albiflorin, paeonol, ${\beta}-sitosterol$ and campesterol, benzoic acid, oleanolic acid, hederagenin and ${\beta}-sitosterol$ 3-O-glucoside were isolated and characterized by means of spectral data. Oleanolic acid and hederagenin have been isolated for the first time from the genus Paeonia.

• 생약학회지
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• 제19권2호
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• pp.97-98
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• 1988

A triterpene was isolated from the roots of Agastache rugosa(Labiatae) and identified as 3-O-acetyl oleanolic acid.

• 약학회지
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• 제35권3호
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• pp.147-153
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• 1991

Chemical constituents of fruits, leaves and barks of Acanthopanax senticosus forma inermis were studied. Their fruits have higher contents of crude ash, crude protein, crude fat, fructose and glucose than those of other Acanthopanax species, and contained larger amount of glutamic acid and malic acid among amino acid and organic acid, respectively. The compounds identified from their barks and leaves, were $\beta$-sitosterol and stigmasterol, sesamin, savinin, syringaresinol diglucoside, oleanolic acid, chiisanoside and polyacetytene ($C_9H_{10}O_2$, mp. 62~63).

• Archives of Pharmacal Research
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• 제27권8호
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• pp.840-844
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• 2004

A triterpene was isolated as a cytotoxic principle from the dichloromethane extract of Korean mistletoe (KM； Viscum album colora turn) by repeated silica gel chromatography and recrystalli-zation. In in vitro analysis of cytotoxic activity using various human and murine tumor cell lines, the dichloromethane extract of KM was highly cytotoxic against these cells. We isolated the most active compound, referred to VD-3, from the dichloromethane extract of KM. The VD-3 was shown to be less cytotoxic to normal cells (murine splenocytes). From the identification of the chemical structure of VD-3 by spectral data and chemical synthesis, the compound was proven to be epi-oleanolic acid. Tumor cells treated with VD-3 showed a typical pattern of apo-ptotic cell death, such as apparent morphological changes and DNA fragmentation. These results indicate that epi-oleanolic acid is an important compound responsible for antitumor activity of KM.

• 생약학회지
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• 제22권1호
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• pp.18-21
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• 1991

Campanulin, ${\alpha}-amyrin$, ${\beta}-amyrin$, uvaol, simiarenol, ursolic acid and oleanolic acid were isolated from the ethyl acetate fraction of the leaves of Rhododendron brachycarpum and their structures were identified by spectroscopic and chemical methods.

• 생명과학회지
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• 제20권3호
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• pp.321-325
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• 2010

구강에 상주하는 미생물 중, Streptococcus mutans는 충치 및 치주염의 원인인 치아플라그를 형성하는데 중요한 역할을 한다. Phytochemical은 식물에서 추출된 화학성분으로서, 사람의 건강에 유익한 영양물질로서 많은 연구들이 진행되어왔다. 본 연구는 이 phytochemical이 중요 구강미생물인 S. mutans에 대한 효과를 살펴보았다. 최근에 Thomson seedless raisin에서 여러 phytochemicals가 추출되었는데, 그 중 oleanolic acid (OA)와 5-(hydroxymethyl)-2-furfural (HF)의 임상적으로 중요한 여러 미생물에 대한 항균활성효과를 확인한 결과, OA가 그람음성균들에게는 항균활성효과가 나타나지 않았고, 그람양성균들에만 항균활성효과를 보였다. 그러나, HF의 경우에는 모든 균주에 대해 항균활성을 나타내지 않았다. 또한, OA는 S. mutans 균주의 표면부착과 생균막의 형성을 저해하기도 하였다. 따라서, 이 연구결과들은 OA가 치아에 존재하는 S. mutans의 생육 및 여러 생리적 특성들을 저해하므로 항플라그제나 항충치약으로서의 활용가능성을 확인할 수 있었다.

• 치위생과학회지
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• 제11권1호
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• pp.37-40
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• 2011

Triterpenoid saponins 유도체인 OA와 UA가 치아우식증 원인균종의 하나인 Streptococcus downei의 표준균주(ATCC $33748^T$) 및 임상균주(4주)에 대하여, 액체배지희석법을 이용한 MIC값 측정 및 time-kill 분석법을 통한 살균작용 유무를 측정하여 다음과 같은 결과를 얻었다. 1. S. downei ATCC $33748^T$ 및 S. downei 임상균주(4주)들의 OA 대한 MIC 값은 $8{\mu}g/ml$로 동일하였고, UA의 대한 MIC 값은 S. downei 표준균주와 임상균주 간에 차이가 있었다. 2. Time-kill 분석법을 실시한 결과 OA와 UA는 S. downei $33748^T$에 대하여 $2{\times}MIC$ (각각 $16{\mu}g/ml$과 $8{\mu}g/ml$) 이상의 농도에서 살균작용을 갖는다는 것을 알 수 있었다. 이상의 연구결과를 종합할 때, triterpenoid saponins 유도체인 OA와 UA는 뮤탄스 연쇄상구균 중 최근에 사람의 구강 내 치면세균막에 서식하는 것으로 밝혀진 S. downei,에 대해 살균제로 작용할 수 있음을 알 수 있었다.