• 제목/요약/키워드: compositae

검색결과 416건 처리시간 0.037초

민간약 "들국화"의 생약학적 연구 (Pharmacognostical Studies on the Folk Medicine 'DulGugWha')

  • 박종희;박성수;배지영
    • 생약학회지
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    • 제41권1호
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    • pp.1-5
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    • 2010
  • Korean folk medicine 'DulGugWha' has been used to cure common cold, cough and chronic and acute gastiritis in Korea. The botanical origin of the crude drug has never been studied pharmacognostically. To clarify the botanical origin of 'DulGugWha', the morphological and anatomical characteristics of Chrysanthemum species growing in Korea, i.e. C. boreale, C. indicum, C. zawadskii and C. zawadskii var. latilobum were studied. As a result, 'DulGugWha' was proved to be the whole plant body of Chrysanthemum boreale of Compositae.

감국(Chrysanthemi Flos)의 새로운 알킬알콜배당체 성분에 관한 연구 (A New Alkyl Alcohol Glycoside from Chrysanthemi Flos)

  • 정근영;오세량;김천석;김정희;이형규
    • 생약학회지
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    • 제27권1호
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    • pp.15-19
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    • 1996
  • In the course of phytochemical studies of Chrysanthermi Flos(Chrysanthemum indicum L., Compositae), two compounds were isolated by repeated column chromatography. Compound 1 is identified as adenosine on the basis of spectroscopic means and comparison with an authentic standard. Compound 2 is determined to be a new alkyl alcohol glycoside, 1-octen-3-ol $3-O-{\beta}-D-xylopyranosyl(1{\rightarrow} 6)-{\beta}-D-glucopyranoside$ on the spectroscopic evidence. Compounds 1 and 2 are reported for the first time from this plant.

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한국산 창출의 성분연구 (Phytochemical Study on the Rhizome of Atractylodes japonica from Korea)

  • 임동술;유승조;지형준
    • 생약학회지
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    • 제19권4호
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    • pp.228-232
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    • 1988
  • From the rhizome of Atractylodes japonica Koidzumi (Compositae) which is the original plant of oriental medicine 'Cang-Zhu', four essential oil compounds were isolated. Three of them were identified as atractylon, hydroxyatractylon and $5{\alpha}H,\;10{\beta}-selina-4(14),\;7(11)-diene-8-one$, which were already known as the constitutents of Atractylodes Rhizoma. The fourth is a novel polyacetylene type compound, and the structure is postulated as 1, 4-diacetoxytetradeca-6, 12-diene-8, 10-diyne by the spectral data.

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포공영의 자유라디칼 소거 및 간세포 보호활성 (In Vitro Free Radical Scavenging and Hepatoprotective Activities of Taraxacum mongolicum)

  • 백흠영
    • 생약학회지
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    • 제34권4호통권135호
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    • pp.324-326
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    • 2003
  • The methanol (MeOH) extract and ist fractions of Taraxacum mongolicum (Compositae) were examined for their scavenging effects on 1,1-diphenyl-2- phenylhydrazyl (DPPH) and superoxide radicals, and hepatoprotective effects on tacrine-induced cytotoxicity in human hepatoma cell line, Hep G2 cells. Both methylene chloride $(CH_2Cl_2)$ and butanol (n-BuOH) soluble fractions of the MeOH extract showed the free radicals scavenging and hepatoprotective effects. From these results, it is suggested that hepatoprotective effect of these fractions partly relies on their free radical scavenging activity.

누로의 생약학적 연구 (Pharmacognostical Studies on the 'NuRo')

  • 박종희;이유진;배지영;김성룡
    • 생약학회지
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    • 제40권3호
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    • pp.161-164
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    • 2009
  • 'NuRo (漏蘆)' is one of the crude drugs which has been used for removal of fever and skin disease. With regard to the botanical origin of 'NuRo', it has been considered to be Echinops species of Compositae, but there has no pharmacognostical confirmation on it. To clarify the botanical origin of 'NuRo', the anatomical characteristics of the root of Echinops latifolius and E. setifer were studied. As a result, it was clarified that 'NuRo' from Korea was the root of Echinops setifer.

Cytotoxic Terpenes and Lignans from the Roots of Ainsliaea acerifolia

  • Choi Sang-Zin;Yang Min-Cheol;Choi Sang-Un;Lee Kang-Ro
    • Archives of Pharmacal Research
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    • 제29권3호
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    • pp.203-208
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    • 2006
  • The chromatographic separation of the MeOH extract of the roots of Ainsliaea acerifolia (Compositae) led to the isolation of six known terpenes and two known lignans. Their structures were identified by spectroscopic methods as mokko lactone (1), betulonic acid (2), betulinic acid (3), zaluzanin C (4), $1{\beta}-hydroperoxygermacra-4(15)$, 5, 10(14)-triene (5), pluviatilol (6), (+)-syringaresinol (7), and glucozaluzanin C (8). Compounds $1{\sim}4$ and 8 showed non-specific significant cytotoxicity against five human tumor cell lines with $ED_{50}$ values ranging from $0.36{\sim}5.54{\mu}g/mL$.

목향(Saussureae Radix)으로부터 Costunolide의 분리 및 함량분석 (Isolation and Quantitative Determination of Costunolide from Saussurea Root)

  • 김주선;지형준;장승엽;하광원;강삼식
    • 생약학회지
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    • 제30권1호
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    • pp.48-53
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    • 1999
  • Isolation and quantitative determination of costunolide from Saussurea lappa Clarke (Compositae) has been conducted by using HPLC method. Costunolide in an acetone extract from the crude drug was separated on a RP-18 column using a $MeOH-H_20$ mixture (65:35) as an eluent and the average content is about $1.32{\sim1.42%.$ The content of costunolide in dried extract was decreased by about 24% in seven days. However it showed a slight decrease in solution. It is highly recommended that quantitative determination of costunolide from Saussureae Radix should be conducted as early as possible after solvent extraction.

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The Constituents of Siegesbeckia orientalis

  • Xiong, Jiang;Ma, Yunbao;Xu, Yunlong
    • Natural Product Sciences
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    • 제3권1호
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    • pp.14-18
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    • 1997
  • Two new diterpenoids, orientalin A (1), and B (2), have been isolated together with six known compounds, kirenol (3), $ent-16{\beta},17-dihydroxykauran-19-oic$ acid (4), $ent-16{\beta},17-dihydroxykauran-19-oic$ $acid-16{\beta},l7-acetonide$ (5), $3,7-dimethylquercetin$ (6), ${\beta}-sitosterol$ (7), and daucosterol (8) from the ethanol extract of Siegesbeckia orientalis (Compositae). Their chemical structures have been elucidated as $ent-15-acetoxy-2{\alpha},16,19-trihydroxypimar-8(14)-ene$ (1), $ent-16-acetoxy-2{\alpha},15,19-trihydroxypimar-8(14)-ene$ (2), respectively, on the basis of chemical and spectral evidence.

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미국가막사리 지상부의 항산화 성분 (Antioxidant Components of the Aerial Parts of Bidens frondosa L.)

  • 안달래;김대근
    • 생약학회지
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    • 제47권2호
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    • pp.110-116
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    • 2016
  • As a part of an ongoing search for natural plants with antioxidant compounds by measuring the radical scavenging effect on 1,1-diphenyl-2-picrylhydrazyl (DPPH), a total extract of the aerial parts of Bidens frondosa L. (Compositae) was found to show potent antioxidant activity. Subsequent activity-guided fractionation of the methanolic extract led to the isolation of five compounds, quercetin-3-O-${\beta}$-D-glucopyranoside (1), luteolin-7-O-${\beta}$-D-glucopyranoside (2), 7,8,3',4'-tertrahydroxy-flavanone (3), okanin-4-O-${\beta}$-D-glucopyranoside (4), and okanin (5). Their structures were elucidated by spectroscopic studies. Compounds 3-5 were isolated for the first time from this plant. Among them, compounds 3 and 5 showed the significant radical scavenging effects on DPPH, and compounds 3 and 5 also showed the potent riboflavin and xanthine originated superoxide quenching activities.

고지방 식이 흰쥐에서 섬쑥부쟁이 Caffeoylquinic Acid 고함유 추출물의 동맥경화 위험지수, 산화적 스트레스 및 체중에 대한 효과 (The Extract of Aster glehni Leaves Rich in Caffeoylquinic Acids Prevents Atherogenic Index, Oxidative Stress, and Body Weight Increase in High-Fat Diet-induced Rats)

  • 김명회;누그로호 아궁;최종원;박희준
    • 생약학회지
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    • 제42권1호
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    • pp.54-60
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    • 2011
  • In an attempt to find the activity of Aster glehni (Compositae) leaves on the obesity in vivo, 30% ethanolic extract rich in caffeoylquinic acids was orally treated with 100 and 200 mg/kg for consecutive four weeks during feeding high-fat diet in rats for 6 weeks. This extract prevented the increase of atherogenic index and body weight and oxidative stress from dietinduced obese rats probably due to the pharmacological mechanism of the CQ complex.