• 식물분류학회지
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• 제44권4호
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• pp.261-275
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• 2014

한국산 산박하속(Isodon)에 대하여 최근 몇몇 종에 있어서는 종내 분류군의 구분에 대한 연구가 이루어진 바 있지만, 현재까지 한국산 종들의 형태학적 형질에 대한 종합적 고찰은 이루어진 바는 없다. 본 연구에서는 지금까지 한반도에 자생한다고 보고된 분류군들에 대하여 한국 및 일본의 주요 표본관으로부터 대여한 약 600여점의 표본을 조사하여 외부형태학적 형질들 도출해 내고, 각각의 형질에 대한 형질상태의 유형을 파악하여 도해하였다. 그 결과 한국산 산박하속은 4종 2변종 1품종으로 정리되었고, 한국산 분류군들을 구분할 수 있는 기존의 문헌상의 식별형질들을 재확인 하였으며, 또한 새로운 식별형질들을 제시하였다: 1) 줄기에 있는 털의 높은 밀도(줄기 한쪽 면에 70개/mm 이상)는 털산박하(I. inflexus var. canescens)를 다른 분류군들로 부터 구분하는 형질이었고, 2) 잎 뒷면의 선모의 높은 밀도(40개/$mm^2$ 이상)는 I. serra와 다른 분류군을 구분할 수 있는 형질이었으며, 3) 화관에 있어서 하순으로부터 암술과 수술이 하순길이 이상으로 돌출하는 것은 I. japonicus 만의 특징이었으며, 4) 과실표면 전체에 비선모가 존재하는 것은 I. inflexus var. microphyllus만의 식별형질이었다.

• Bulletin of the Korean Chemical Society
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• 제23권4호
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• pp.617-618
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• 2002

• Natural Product Sciences
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• 제4권1호
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• pp.38-41
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• 1998

From the dried leaves of Isodon eriocalyx (Labiatae) six flavonoids were isolated and two of them were elucidated to be novel ones named 5,7,8,4'-tetrahydroxy-6-methoxyflavone (1), and $isothymusin-8-O-{\beta}-D-glucoside$ (2).

• 식물분류학회지
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• 제41권3호
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• pp.223-229
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• 2011

The taxonomy of the Isodon excisus complex has been ambiguous and problematic because the morphological characters, especially characters related to the leaf distinguishing subgroups of the complex in the original descriptions, are variable. To elucidate the taxonomic structure of the I. excisus complex in Korea, 34 characters were measured from 70 OTUs representing different locations and analyzed by principal component analysis (PCA). The analysis showed that principle component axis 1, 2, 3 (PC1, PC2, PC3) represents 52.0% of the total variance and characters showing high loading values for PC1 were leaf shape, density of non-glandular hairs on the lower surface of the leaf, and characters related to the teeth of the leaf. The length of apical tooth and the angle between two widest points of the leaf were highly correlated to PC2 and PC3, respectively. Three-dimensional scatter plotting of OTUs for PC1, PC2, and PC3 axis showed that the areas of previously recognized three subgroups of I. excisus completely overlapped. Our result supported that just one taxon, I. excisus var. excisus, should be recognized in the complex at the variety level.

• 생약학회지
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• 제34권2호통권133호
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• pp.132-137
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• 2003

The effect of aqueous extract of Isodon japonicus Hara (Labiatae) (IJAE) on mast cell-mediated immediate-type allergic reactions was investigated. IJAE inhibited compound 48/80-induced systemic anaphylaxis and immunoglobulin E (IgE)-mediated local anaphylaxis. When IJAE was pretreated at the same concentration with systemic anaphylaxis, serum histamine levels were reduced in a dose-dependent manner. IJAE dose-dependently inhibited histamine release from rat peritoneal mast cells (RPMC) activated by compound 48/80. The level of cAMP in human mast cell line (HMC-1) cells, when IJAE was added, significantly was increased, compared with that of normal control. These results indicate that IJAE will beneficial in the treatment of immediate-type allergic reaction.

• Natural Product Sciences
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• 제4권3호
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• pp.143-147
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• 1998

Examination of the chemical constituents of the dried leaves of Isodon eriocalyx (Dunn.) Hara led to the isolation of four new diterpenoids, named maoecrystal Q-T (1-4). Their structures were elucidated as $16(R)-methoxymethyl-6{\beta},\;7{\beta}-dihydroxy-7{\alpha},20-epoxy-ent-kaur-2,3-ethenylene-1$, 15-dione(1), $1{\beta},18-diacetoxy-6{\beta},7{\beta}-dihydroxy-7{\alpha},20-epoxy-ent-kaur-16-en-15-one\;(2),\;6{\beta},\;7{\beta}-dihydroxy-15{\beta}-acetoxy-7{\alpha},20-epoxy-ent-kaur-16-en-1-one$ (3) and $7{\beta}-hydroxy-6{\beta},15{\beta}-diacetoxy-1{\alpha},11{\beta}-acetonide-7{\alpha},20-epoxy-ent-kaur-16-ene$ (4), respectively, on the basis of spectroscopic methods. Meanwhile, five known diterpeonids eriocalyxin B (5), maoecrystal B-D (6-8) and trichokaurin (9) were also obtained.

• Archives of Pharmacal Research
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• 제20권3호
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• pp.291-296
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• 1997

The studies were carried out to evaluate the constituents in the aerial part of Isodon excisus var. coreanus (Labiatae). From the aqueous fraction of methanol extract, compound I (${\alpha}$-[[3-(3, 4-dihydroxyphenyl)-1-oxo-2-propenyl]oxy]-3,4-dihydroxy-benzenepropanoic acid), compound II (9-methyl-dihydroferulic acid-4-O-.betha.-D-glucopyranosyl $(1{\rightarrow}2)$-${\alpha}$-L- rhamnopyranosyl (1.rarw.4)-.betha.-D-glucopyranoside), compound III (ent-7.alpha., 11${\alpha}$,15.betha.-trihydroxy-kaur-16-en-1-O-.betha.-D-glucopyranoside) and compound IV ($2{\alpha}$,3${\beta}$,$7{\alpha}$,23-tetrahydroxy-olean-12 -en-28-oic acid 28-O-${\beta}$-D-glucopyranoside) were isolated and identified on the basis of their physicochemical and spectroscopic evidences[IR, FAB(-)MS,$^{1}H-NMR,$$^{13}C-NMR,$$ HMQC$$^{1}H-^{1}H $COSY and HMBC (Heteronuclear Multiple Bond Connectivity)]. Especially, New compounds II and III were named Isodonin A and Isodonin B respectively.

• 한국식품영양학회지
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• 제9권2호
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• pp.137-142
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• 1996

To develop antioxidant substances in plant, phenolic compounds in Bangah (Igodon japonicus, Hara) and antioxidative effects of cell extracts were investigated. Defatted samples of Bangah were extracted with acetone/methanol and the extracts were fractionated Into the free and bound types of phenolics. The equal amounts of fractions were dissolved In soybean oil and autoxidized at 45$^{\circ}C$ for 25 days. Peroxide value and TBA values were determined every 5 days during oxidation. Changes of peroxide and TBA values showed antioxidant effects, which were lower than control during the oxidation periods. The effects of cell extracts were evaluated as high as BHT, 0.02 ppm. The antioxidative effect of insoluble-bound phenolic extract was higher than that of free. The contents of phenolic compounds in insoluble-bound fraction were also higher than free fraction.

• Archives of Pharmacal Research
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• 제23권3호
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• pp.243-245
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• 2000

The diethyl ether extract of isodon excisus var. coreanus exhibited significant inhibitory activity in aromatase assay. Bioactivity-guided fractionation of the extract led to the isolation of three active compounds: inflexin(ent-1${\alpha}$-hydroxy-3${\beta}$,6a-diacetoxykau r-16-en-11,15-dione) (1), ursolic acid (2), and ursolic acid 3-O-acetate (3).

• 대한약학회:학술대회논문집
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• 대한약학회 2000년도 NEW STRATEGY FOR DRUG DEVELOPMENT IN POST-GENOMIC ERA(대한약학회)
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• pp.229.3-230
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• 2000