• Title/Summary/Keyword: ROSACEAE

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Triterpenoids from the Roots of Rubus parvifolius

  • Choi, Yoon-Soo;Son, Kun-Ho;Do, Jae-Chu
    • Archives of Pharmacal Research
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    • v.14 no.3
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    • pp.225-230
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    • 1991
  • From the roots of Rubus parvifolius L., four triterpenoidal sapogenins, ursolic acid 1. $2\alpha$-hydroxyursolic acid 2. causapic acid 3. $2\alpha$, $3\beta$, $19\alpha$-trihydroxyurs-12-en-23.28-dioic acid 4 and one triterpenoidal glycoside. suavissimoside $R_1$ 5. were isolated. The structures were elucidated by spectroscopic methods and chemical transformations. Compound 4 was first isolated as free form.

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Chemical Investigation of the Constitutive Flavonoid Glycosides of the Leaves of Crataegus sinaica

  • El-Mousallamy, Amani M. D.
    • Natural Product Sciences
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    • v.4 no.2
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    • pp.53-57
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    • 1998
  • Leaves of Crataegus sinaica Boiss, contain the new C-glycosyl flavone $3"',4”’-di-O-acetyl-2“-O-{\alpha}-rhamnosylvitexin$, together with the hitherto unknown, dihydroflavonol 3-O-xyloside, (2R:3R)-dihydroquercetin-$3-O-{\beta}-xylopyranoside$. The known compounds (+)-catechin, (-)-epicatechin, vicenin-II, $2"-O-{\alpha}-rhamnosylvitexin$, and $4"'-O-acetyl-2"-O-{\alpha}-rhamnosylvitexin$ were also characterized. Structures were established by conventional methods of analysis and confirmed by $^1H-,\;^{13}C-NMR$, and ESI-MS.

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Pharmacognostical Studies on the Korean Folk Medicine 'Jin Hae Cho' (민간약 "진해초"의 생약학적 연구)

  • Park, Jong-Hee;Do, Jin-Kyoung
    • Korean Journal of Pharmacognosy
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    • v.25 no.2
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    • pp.178-187
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    • 1994
  • Korean folk medicine 'Jin Hae Cho' has been used as a remedy for neuralgia and an invigorating drug after a childbirth in Korea. The botanical origin of the crude drug has been no pharmacognostical confirmation on it. To clarify the botanical origin of 'Jin Hae Cho', studied on the morphological and anatomical characteristics of the roots of Potentilla species growing wild in Korea i.e. Potentilla chinensis Ser., P. cryptotaeniae Maxim., P. dickinsii Fr. et Sav., P. discolor Bunge, P. fragarioides L. var. major Maxim., P. freyniana Bornm., P. kleiniana Wight et Arnott, P. paradoxa Nutt., P. yokusaiana Makino and 'Jin Hae Cho' from Korea on Korean market. As a result, it was made clear that 'Jin Hae Cho' from Korea was derived from the roots of Potentilla chinensis Ser. and Potentilla discolor Bunge.

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In vitro screening of 3-hydroxy-3-methy1g1utaryl-Coenzyme A reductase inhibitor from plant extracts (식물 추출물로 부터 3-hydroxy-3-rnethylglutaryl-Coenzyme A Reductase의 활성저해제 탐색)

  • 이윤형;신용목
    • KSBB Journal
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    • v.6 no.1
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    • pp.55-61
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    • 1991
  • The objective of this in vitro study is to screen a possible inhibitor, originated from some chinese herb medicines, of 3-hydroxy-3-methylglutaryl Coenzyme A (HMG-CoA) reductase that is the major regulatory enzyme of hepatic cholesterol biosynthesis. Fourteen kinds of herbal plant were extracted with water and evaporated for prescreening. The methanol extracts of the effective 3 kinds (9 species) were fractionated with chloroform, ethylacetate, butanol and water, and vacuum evaporated. The degree of inhibition of the extracts to HMG-CoA reductase activity was calculated by the spectrophotometric method using microsomal protein of Saccharomyces cerevisiae ATCC 42949 as an enzyme source. Among these samples, marked inhibitory effects were observed in the extracts of ethylacetate and chloroform fractions of the Rosa rugosa roots, and those of butanol, ehtylacetate and water fractions of pine leaves. Also, the inhibitory effects of the extracts obtained from buckwheat shell and the roots of Rosaceae were found.

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Phenolic Compounds from Leaves of Spiraea salicifolia (꼬리조팝나무 잎의 페놀성 화합물)

  • Ahn, Byung-Tae;Oh, Kap-Jin;Park, Si-Kyung;Chung, Sun-Gan;Cho, Eui-Hwan;Kim, Jae-Gil;Ro, Jai-Seup;Lee, Kyong-Soon
    • Korean Journal of Pharmacognosy
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    • v.27 no.3
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    • pp.178-183
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    • 1996
  • Seven phenolic compounds were isolated from the leaves of Spiraea salicifolia. Their structures were characterized as cinnamic acid, ${\rho}-hydroxy$ cinnamic acid, ${\rho}-methoxy$ cinnamic acid, $1-O-coumaroyl-{\beta}-D-glucopyranose$, $1-O-caffeoyl-{\beta}-D-glucopyranose$, hyperoside and quercetin $3-O-(6'-O-{\alpha}-L-arbinopyranosyl)-{\beta}-D-galactopyranoside$ by chemical and spectroscopic evidence.

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Anti-HIV-1 Protease Activity and in Vivo Anti-lipid Peroxidative Effect on Rosa davurica (생열귀나무의 항 HIV-1 protease 작용과 생체내 과산화지질생성 저해효과)

  • Kim, Suk-Nam;Chang, Kwang-Jin;Choi, Jong-Won;Park, Jong-Cheol
    • Korean Journal of Pharmacognosy
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    • v.31 no.3
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    • pp.264-267
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    • 2000
  • Anti-human immunodeficiency virus (HIV) type I protease (PR) and anti-lipid peroxidation effects on Rosa davurica were investigated. Of the various parts tested from R. davurica, the water extracts of stem and leaves inhibited the HIV-1 PR activity by more than 45% at a concentration of $100\;{mu}g/mL$. Hyperoside from the percarp of title plant showed 25% inhibition on HIV-1 PR at $200\;{mu}M$. The methanol extract of the root of R. davurica reduced the level of lipid peroxides induced by bromobenzene in vivo.

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Parmacognostical Studies on the Korean Folk Medicine "Ma Ga Mog" (민간약 "마가목"의 생약학적 연구)

  • Park, Jong-Hee;Do, Won-Im;Kim, Mi-Hee
    • Korean Journal of Pharmacognosy
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    • v.40 no.1
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    • pp.32-34
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    • 2009
  • Korean folk medicine 'Ma Ga Mog' has been used as a remedy for rheumatis, cough and bronchitis in Korea. The botanical origin of the crude drug has been no pharmacognostical confirmation on it. To clarify the botanical origin of 'Ma Ga Mog', the anatomical characteristics of the bark of Sorbus amurensis Koehne, S. commixta Hedl. and S. sambucifolia (Cham. et Schltdl.) Roemer var. psuedo-gracilis C. K. Schneid. were studied. As a result, it was clarified that 'Ma Ga Mog' from Korea was the bark of Sorbus amurensis Koehne and S. commixta Hedl.

EFFECTS OF SPIRAMINE ALKALOIDS ON THE PLATELET AGGREGATION

  • jiang, Hao-Xiao
    • Proceedings of the Korean Society of Applied Pharmacology
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    • 1998.11a
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    • pp.66-71
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    • 1998
  • Spiraea japonica L. F., a plant species belongs to the Spiraea genus of Rosaceae family, has seven varieties. There are all varieties distributed in Yunnan province of China, and S. japonica var. acuminata and S. japonica var. fortunei were used as the folk medicines to treat malaria and inflammation etc.. Since 1960s, Japanese and Russian scholars obtained C$\_$20/-diterpenoid alkaloids from S. japonica L.F., also Chinese scholars got a series of Hetisine-type C$\_$20/-diterpenoid alkaloids from S. japonica var. fortunei in 1985. Since then, we started the chemical and pharmaceutical studies of this complex. Here we wish to report the bioactive effects of spiramine alkaloids and their derivatives on the platelet aggregation induced by AA, PAF, or ADP.

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A Basic Study on Development of Medical Wild Plant Resouces in Mt. CHU-WOL (추월산 한약자원식물의 분포 및 분류체계에 관한 기초적 연구)

  • EuiSooYoon
    • Korean Journal of Plant Resources
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    • v.3 no.1
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    • pp.41-63
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    • 1990
  • The plants medicinal resources of Mt. Chu-woL were investigated 21times from APril, 1975 to August , 1977 and from JuLy, 1988 to August 1989In orther to analyze the vegetation of Chu-woL mountain area , medical wildplants structure and distribution. MedicaL wild plants of Chu-woL moun-tain consisted of 113 familis, 428 species in alL. The resources of important herb drugs were Polypodiaceae, Graminea, Liliaceae , Polygonaceae,Ranunculaceae, Brassicaceae, Rosaceae , Fabaceae, Apiaceae, tabiatae, so-lanaceae, Scrophulariaceae, Campanulaceae, Compositae. The herb drugswere comparatively more than in other mountains in our country .

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A Phenolic Glucoside Isolated from Prunus serrulata var. spontanea and its Peroxynitrite Scavenging Activity

  • Jung Hyun Ah;Chung Hae Young;Kang Sam Sik;Hyun Sook Kyung;Kang Hye Sook;Choi Jae Sue
    • Archives of Pharmacal Research
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    • v.28 no.10
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    • pp.1127-1130
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    • 2005
  • A new phenolic glucoside (1), pursargentoside, was isolated from the leaves of Prunus serrulata var. spontanea, along with three other known compounds, orobol 7-O-glucoside (2), $1{\beta}$, $2{\alpha}$, $3{\alpha}$, 24-tetrahydroxy-urs-12-en-28-oic acid (3), and chlorogenic acid (4). The structure of pursargentoside (1) was identified by spectroscopic data analysis including 1D and 2D NMR spectroscopy, as 2-O-${\beta}$-(6'-benzoyl)-glucopyranosyl o-(Z)-coumaric acid. Compounds 1, 2, and 4 exhibited ONOO- scavenging activity, whereas compound 3 was determined to be virtually inactive.