• Korean Journal of Pharmacognosy
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• v.23 no.4
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• pp.280-282
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• 1992

Quercitrin and hyperin were isolated from the leaves of Kalopanax pictum and these structures were characterized on the basis of chemical and spectral data.

• Archives of Pharmacal Research
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• v.14 no.2
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• pp.124-129
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• 1991

One new triterpenoidal bisdesmoside, saponin C (3) were isolated from the leaves of Kalopanax pictum var. chinense along with two known saponins, saponin B (2, sapindoside C) and saponin A (1, sapoindoside B). On the basis of chemical and spectral evidences, the structure of a new triterpenoidal saponin has been elucidated to be 3-O-$\beta$-D-glucopyranosyl (1$\rightarrow$4)$\beta$-D-xylopyranosyl (1$\rightarrow$3)-$\alpha$-L-rhamnopyranosyl (1$\rightarrow$2)-$\alpha$-L-arabino-pyranosyl-23-hydroxyolean-12-en-28-O-$\alpha$-L-rhamnopyrano syl (1$\rightarrow$4)-$\beta$-D-glucopyranosyl (1$\rightarrow$6)-$\beta$-D-glucopyranosyl ester.

• Archives of Pharmacal Research
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• v.14 no.1
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• pp.19-24
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• 1991

One new triterpenoidal saponin, saponin F(2) has been isolated from the bark of Kalopanax pictum Nakai var. typicum (Araliaceae), together with one known saponin, kizuta saponin $K_{12}$ (1). On the basis of chemico-spectral evidences, the structure of 2 has been elucidated to be 3-O-${\beta}$-D-xylopyranosyl$(1{\rightarrow}3)$-${\alpha}$-L-rhamnopyranosyl$(1{\rightarrow}2)$-${\alpha}$-L-arabinopyranosyl-23-hydroxyolean-12-en-28-O-${\alpha}$-L-rhamnopyranosyl$(1{\rightarrow}4)$-${\beta}$-D-glucopyranosyl$(1{\rightarrow}6)$-${\beta}$-D-glucopyranosyl ester.

• Archives of Pharmacal Research
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• v.14 no.1
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• pp.7-11
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• 1991

Three triterpenoid saponins were isolated from the methanol extract of the stem bark of Kalopanax pictum Nakai var. magnificum (Araliaceae). The structures of these saponins were identified as hederagenin 3-O-${\alpha}$-L-arabinopyranoside, hederagenin-3-O-${\alpha}$-L-rhamnopyranosyl$(1{\rightarrow}2)$-${\alpha}$-L-arabinopyranoside and 3-O-${\alpha}$-L-rhamnopyranosyl(1{\rightarrow}2)-${\alpha}$-L-arabinopyranosyl hederagenin 28-O-${\alpha}$-L-rhamnopyranosyl$(1{\rightarrow}4)$-${\beta}$-D-glucopyranosyl$(1{\rightarrow}6)$-${\beta}$-D-glucopyranosyl ester.

• Korean Journal of Pharmacognosy
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• v.17 no.1
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• pp.78-84
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• 1986

Among the Araliaceae plants indigenous to Korea, those whose medicinal usage are comparatively high have been selected in this serial studies. Chiisanoside and acanthoside D were isolated and identified from the Acanthopanax chinensis leaves and root bark. Chiisanoside and acanthoside D have been found to have the lowering S-GPT, S-GOT value and BSP-retention rate and survival rate, anti-histaminic effect in the toxic state through the bio-pharmacological experiments. ${\alpha}-hederin$, hederagenin pentaglycoside were isolated both stem bark of Kalopanax pictum Nakai var. magnificum and Kalopanax pictum Nakai var. Max. respectively. Syringoside, acanthoside D were also isolated from the root bark of Acanthopanax koreanum. The biological activity of ginsenoside $Rb_1$, $Rg_1$, Re were examined. Ginsenoside $Rb_1$, $Rg_1$, Re promotes the antileaking effect in X-ray (Co 60) irradiated toxic state.

• Korean Journal of Environment and Ecology
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• v.19 no.2
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• pp.188-192
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• 2005

To seek for proper regeneration methods with under-planting, Photosynthetic rate and chlorophyll contents of three broad-leaved species seedlings, Kalopanax pictum, Fraxinus rhynchophylla and Cornus controversa, were measured and compared between growing sites, below the canopy of Larix kaemferi and open land in the forest. Nursery stocks was planted in open nurs- ery in the forest in late April, 1997, and under-planting below the canopy of Larix kaemferi was conducted in late April, 1998. This experiment examined the relationships between shade-tolerance and physiological response to different light environment by tree species. To adapt the shade environment, leaves of Kalopanax pictum might be increased the more chlorophyll con- tents and photosynthetic ability than other species. From these results, shade-tolerance of the tree might be ordered Kalopanax pictum, Fraxinus rhynchophylla, and Cornus controversa.

• Journal of Pharmaceutical Investigation
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• v.5 no.1
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• pp.23-27
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• 1975

Hederine, m. p. $256{\sim}257^{\circ}\;C_{41}H_{64}O_{11}\;{\cdot}\;2H_{2}O$ : $23-hydroxy-3{\beta}-({\beta}-{\alpha}-arabinosidor hamnoside)-olenana-12-ene-oique,$ was obtained from the cortex of Kalopanax pictum. Acid hydrolysis of hederine yielded hederagenin, arabinose and rhamnose. Hederagenin was identified by comparison of it's mixed melting point and IR spectra against authentic sample. Arabinose and rhamnose were identified by TLC against standards.

• Journal of Pharmaceutical Investigation
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• v.4 no.4
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• pp.5-16
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• 1974

Liriodendrin, m. p. $269-270^{\circ}$, $C_{22}$ $H_{46}$ $O_8$ as one of the antihypertensive components was obtained from the cortex of Kalopanax pictum. Acid hydrolysis of liriodendrin yielided liriresinol-A, -B and glucose. The stereochemistry of liriodendrin was established by the NMR spectrum of liriodrin octaacelate. The NMR spectrum of liriodendrin octaacetate showed that $di-{\beta}-glucoside$ of lirioresinol-B type occurs in nature.

• Korean Journal of Weed Science
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• v.7 no.3
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• pp.289-298
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• 1987

This study was conducted to investigate the presence of biologically active substances such as phenolic acids, fatty acids and organic acids in the medical plants like Kalopanax pictum and Acanthopanacis cortex. Alcohol extracts of K. pictum and A. cortex showed complete inhibition of lettuce seed germination, indicating that these plants contained the biologically active substances. Eleven phenolic acids including protocatechuic acid were identified from K. pictum and A. cortex by GLC, and the contents of total phenolic acid were 1.7917mg/g in K. pictum, and 0.9567mg/g in A. cortex. Polyphenols such as neochlorogenic acid, chi orogenic acid, scopoletin, rutin and kaempferolglycoside which were not detected by GLC were anayzed by HPLC, and among phenolic acids indentified chi orogenic acid seemed to be the major acid in both K. pictum and A. cortex presented in amount of 23.7 and 13.0ppm, respectively. K. pictum contained 5.26mg/g of fatty acids and 27.69mg/g of organic acids, and A. cortex possessed 3.22mg/g of fatty acids and 9.80mg/g of organic acids, linoleic and oxalic acid appeared to be the major fatty and organic acids, representing more than 50% of total fatty acids and 80% of total organic acids.

• Journal of Korean Society of Forest Science
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• v.87 no.3
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• pp.483-492
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• 1998

The objective of this study was to investigate the site and growth characteristics of Kalopanax septemlobus mixed with other hardwoods growing at Mt. Joongwang area located in Pyungchang-gun, Kangwon-do. The K. septemlobus stands were located at 1,000m to 1,200m in altitude, steep slope, and ridge-slope areas with aspects facing northeast to northwest. The K. septemlobus stands showed deep A soil layer with high soil moisture and soil nutrients. Major over-story species were Quercus mongolica, Acer pictum, Acer pseudosieboldianum and Carpinus cordata. The herbaceous vegetation was predominantly consisted with Pimpinella brachycarpa, Meehania urticifolia, Ainsliaea acerifloia and Polystichum species. The annual mean diameter increment of K. septemlobus was 2.4mm/year, with high diameter growth at lower altitude, south aspect and valley areas.