• YAKHAK HOEJI
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• v.41 no.2
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• pp.149-152
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• 1997

Three compounds were isolated from the n-BuOH fraction of buds of Eugenia caryophyllata and their structures were identified as 3,3',4-tri-O-methylellagic acid, 3-O--${\beta}$ -D-glucopyranosyl-3,5,4'-trihydroxy-7,3'-dimethoxyflavone and gallic acid by chemical and spectral evidence.

• Archives of Pharmacal Research
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• v.15 no.1
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• pp.62-68
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• 1992

From the roots of Caragana sinica (Buc'hoz) Rehder (Leguminosae), a new saponin named caraganoside A was isolated and elucidated as 3-0-$\beta$-D-xylopyranosyl (1$\rightarrow$2)-[$\beta$-D-glucopyranosyl (1$\rightarrow$3)]-$\alpha$-L-arabinopyranosyl oleanolic acid 28-O-[$\beta$-D-glucopyranosyl ester by means of chemical and spectral studies. Kalopanax-saponin F, hemsloside Ma3 and araloside A were also isolated and characterized. The former two compounds were separated as their methylesters.

• Natural Product Sciences
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• v.11 no.2
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• pp.75-78
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• 2005

A new acetophenone named rumexin $(3-hydroxy-5-methyl-4-O-{\beta}-D-glucopyranosyl\;acetophenone)$ was isolated from methanolic extract of Rumex aquatica together with eight known compounds, $quercetin-3-O-{\beta}-D-glucuropyranoside$, $musizin-8-O-{\beta}-D-glucopyranoside$, $quercetin-3-O-{\alpha}-L-rhamnoside$, $emodin-8-O-{\beta}- D-glucopyranoside$, caffeic acid, $1-O-caffeoyl-{\beta}-D-glucopyranoside$, 1-methyl caffeic acid, $kaempferol-3-O-{\beta}-D-glucuropyranoside$. All of the above compounds were isolated from Rumex aquatica for the first time, and structures of compounds were established by spectroscopic means.

• Korean Journal of Pharmacognosy
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• v.33 no.1 s.128
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• pp.1-4
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• 2002

The phytochemical study of the underground parts of Gardenia jasminoides var. radicans Makino (Rubiaceae) led to the isolation of five coumarins. On the basis of spectroscopic evidences, the structures of these compounds were charaterized as ferulic acid(l), 5,8-di-(3-methyl-2,3-dihydroxybutyloxylpsoralen)(2), skimmin(3), uracil(4), $3-0-{\alpha}-D-glucopyranosyl-(1{\rightarrow}4)-{\beta}-D-glucopyranosyloxypeucedanin$ hydrates(5), respectively.

• Korean Journal of Pharmacognosy
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• v.22 no.3
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• pp.156-161
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• 1991

Four furocoumarins and two dihydrofuranocoumarin glycosides have been isolated from the benzene-soluble and butanol-soluble portions of the roots of Ostericum koreanum Kitagawa, respectively. Four furocoumarins have been determined as imperatorin, isoimperatorin, oxypeucedanin and oxypeucedanin hydrate, and two dihydrofuranocoumarin glycosides determined as marmesinin and $4'-O-{\beta}-D-glucopyranosyl-3'-hydroxymarmesin$ on the basis of spectral data and physico-chemical evidence.

• Proceedings of the Korean Society of Life Science Conference
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• 2003.05a
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• pp.23-37
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• 2003

A novel inhibitor against maltose-producing a-amylase was prepared via stepwise degradation of a high molecular weight acarbose (HMWA) using Thermus maltogenic amylase (ThMA). The structure of the purified inhibitor was determined to be ${\alpha}$-D-glucopyranosyl-${\alpha}$-acarviosinyl-D-glucopyranose (GlcAcvGlc). Progress curves of p-nitrophenyl-${\alpha}$-D-maltoside (PNPG2) hydrolysis by various amylolytic enzymes, including maltogenase (MGase), ThMA, and cyclodextrinase(CDase) I-5, in the presence of acarbose or GlcAcvGlc indicated a slow-binding mode of inhibition. The inhibition potency of GlcAcvGlc for MGase, ThMA, and CDase I-5 was 3 orders of magnitude higher than that of acarbose.

• Archives of Pharmacal Research
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• v.25 no.5
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• pp.621-624
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• 2002

From the leaves of Brassica juncea, a new rare kaempferol 7-Ο-triglucoside isolated and characterized as kaempferol 7-Ο-$\beta$-D-glucopyranosyl-(1longrightarrow3)-[$\beta$-D-glucopyranosyl-(1longrightarrow6)]-glucopyranoside (1) based on the spectroscopic evidences. This compound was found to be a scavenger of 1, 1-diphenyl-2-picrylhydrazyl radical.

• Applied Biological Chemistry
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• v.39 no.6
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• pp.512-516
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• 1996

Sophorose $(2-O-{\beta}-D-glucopyranosyl-D-glucopyranose)$ was chemically synthesized from D-glucopyranose through six steps of chemical reactions with the yield of 21%. The chemical structures of sophorose and some compounds obtained during reactions were confirmed by interpretations of spectral data, NMR, IR, etc.

• Archives of Pharmacal Research
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• v.20 no.2
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• pp.194-196
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• 1997

A C-glycosyl chromone, named as 7-O-methylaloesinol, was newly isolated from the leaf exudate of Aloe capensis and identified as $8-C-{\beta}-D-glucopyranosyl$${\beta}-2-[2-(R)-hydroxypropyl]-7-methoxy-5-methyl-4H-1-benzopyran-4-one$ by chemical and spectral evidence.

• YAKHAK HOEJI
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• v.44 no.4
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• pp.334-339
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• 2000

The present study was carried out to evaluate biologically active components of the rhizomes of Sparganium stoloniferum and to supply the preliminary data for the chemotaxonomy and the medicinal application. Extraction and systematic fractionation of the rhizomes by column chromatography led to the isolation of six compounds from ethylacetate and n-butanol soluble fractions. Elucidation of the chemical structures of these compounds by physicochemical and apectral analysis demonstrated that compound I,II ,III,IV,V and Ⅵ were $\beta$-sitosterol, $\beta$-sitosterol-3-$\beta$-D-glucuronopyranoside, 3- (4-hydroxyphenyl)-2-propenoic acid, sorbose, 1-O-$\beta$-D-glucopyranosyl-(2S, 3R, 4E, 8Z)-2-[(2(R)-hydroxyeicosanoyl)amido]-4,8-octadecadiene-1,3-diol, and $\beta$-sitosterol-3-O-$\beta$-D-glucopyranoside, respectively.