• Archives of Pharmacal Research
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• 제24권6호
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• pp.532-535
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• 2001

A new guaiane type sesquiterpene was isolated from the fruit of Torilis japonica (Umbelliferae). Based on NMR, IR and mass spectroscopy its structure was confirmed as deangeloyloxy torilin, $1{\beta},{\;}7{\alpha},{\;}10{\alpha}$H-11-acetoxy-guaia-4-en-3-one (1). This is the first report showing that this compound can be isolated from Torilis japonica.

• Journal of Ginseng Research
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• 제21권3호
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• pp.214-218
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• 1997

New simple methods for the Isolation of sesquiterpenes from Panax ginseng were developed. First, volatile compounds were isolated by simultaneous distillation and extraction (SDE) with 30% methanol and $\alpha$-hexane instead of water and ethyl ether/pentane (1:1). Secondly, head space volatiles in U-shaped tube at 7$0^{\circ}C$ were passed through C18 Sep-Pak by nitrogen gas streaming and the adsorbed volatiles were fluted by $\alpha$-hexane. TLC analysis showed that the volatile concentrates consisted mainly of terpenes when colored by vanillin-sulfuric and. GC/MS data revealed that approximately 30 sesquiterpenes of molecular weight 204 occupied 81.1% or more of the volatile concentrates isolated by those two newly developed methods. Among these, alloaromadendrene, germacrene B, isocaryophyllene, $\alpha$-neoclovene, ${\gamma}$-muurolene, $\beta$-panaslnsene, and $\alpha$-humulene were identified as being major sesqulterpenes by authentic samples or literatme search Key words : Panax ginseng, volatile compound, sesquiterpene, isolation, new method, GC/MS.

• 생약학회지
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• 제30권1호
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• pp.70-73
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• 1999

Nine sesquiterpene lactones, which were isolated from Hemisteptia lyrata Bunge. Chrysanthemum zawadskii Herbich var. latilobum Kitamura and Chrysanthemum boreale Makino were evaluated for the farnesyl-protein transferase (FPTase) inhibitor, conducted by the scintillation proximity assay (SPA). The angeloylcumambrin B and tigloylcumambrin B inhibited a recombinant rat FPTase with $IC_{50}$ value of $78\;{\mu}g/ml$ $(225\;{\mu}M)$ and $90\;{\mu}g/ml$ $(260 \;{\mu}M)$, respectively.

• Natural Product Sciences
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• 제11권2호
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• pp.55-57
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• 2005

Three known sesquiterpene lactones were isolated from the n-BuOH traction of the roots of Ixeris sonchifolia. Their structures were identified as macrocliniside A (1), glucozaluzanin C (2), and ixerin H (3), by spectral analyses. Compounds 1 and 2 are guaiane-type, while compound 3 is a germacrane-type sesquiterpene lactone. Compounds 1-3 are first isolated from I. sonchifolia.

• 약학회지
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• 제45권2호
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• pp.147-152
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• 2001

The phytochemical study of the aerial parts of Artemisia sylvatica (Asteraceae) led to the isolation of nine sesquiterpene lactones, l$\alpha$-hydroperoxy-rupicolin A acetate (1), rupicolin B acetate (2), rupicolin A acetate (3), l$\alpha$-hydroxy-4$\alpha$-hydroperoxy-bishopsolicepolide (4), 1$\alpha$-hydroperoxy-4$\beta$-hydroxy-8$\alpha$-acetoxy-guaia-2,9,11 (13)-triene-6$\alpha$,12-oxide (5), 1$\alpha$-hydroperoxy-4$\alpha$-hydroxybishopsolicepolide (6), l$\alpha$,4$\beta$-dihydroxy-8$\alpha$-acetoxy-guaia-2,9,11(13)-triene-6$\alpha$,12-olive (7), rupicolin A (8) and l$\alpha$,4$\alpha$-dihydroxy-bishopsolicepolide (9). Their structures were established by chemical and spectroscopic methods.

• Archives of Pharmacal Research
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• 제27권10호
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• pp.1016-1019
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• 2004

The chromatographic separation of a methylene chloride extract of Artemisia rubripes led to the isolation of a new sesquiterpene lactone (3), together with four known compounds, a coumarin (2) and three terpenes (1, 4, and 5). Their structures were characterized to be $1{\beta},6{\alpha}$- dihydroxy-4(15)-eudesmene (1), scopoletin (2), $1{\alpha},4{\beta}-dihydroxy-8{\alpha}$-acetoxy-guaia-2,10(14), 11(13)-triene-6,12-olide (3), $1{\alpha},4{\beta}$ -dihydroxy-8${\alpha}$-acetoxy-guaia-2,9,11(13)-triene-6,12-olide (4), and $\beta$ -sitosterol-3-O-${\beta}$-D-glycoside (5) by spectroscopic means.

• Bulletin of the Korean Chemical Society
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• 제24권5호
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• pp.541-542
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• 2003

• 생약학회지
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• 제24권2호
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• pp.107-110
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• 1993

From the ethanol extract of the leaves of Artemisia selengensis a new sesquiterpene endoperoxide, bisabolene-2,5-endoperoxide, has been isolated. The structure of the peroxide was established on the basis of spectroscopic evidence.

• Bulletin of the Korean Chemical Society
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• 제35권11호
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• pp.3346-3348
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• 2014

• 한국산림과학회지
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• 제110권4호
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• pp.543-553
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• 2021

피톤치드는 식물체에서 방출되는 생물유래 휘발성유기화합물(BVOCs)에 포함되어있는 isoprene, monoterpene, sesquiterpene과 같은 화합물들 형태로 존재한다. 또한 피톤치드는 중요한 산림치유 인자인 동시에 질소화합물과 광학반응을 하여 오존 및 이차 유기에어로졸 생성에 영향을 미치는 물질로 보고되고 있다. 본 연구에서는 우리나라 도시숲 주요 30 수종을 선정하여 표준환경조건(온도: 30℃, 광도: 1,000 μmol/m²/sec)에서 400 L Tedlar bag의 순환형 챔버를 이용하여 시료를 포집하여 열탈착-GC/MS로 분석하였고, 해당 수종의 잎을 건조시켜 건중량 당 수종별 isoprene 및 terpene류의 방출량을 분석하였다. Isoprene 방출량은 전체 수종 중에서 왕대에서 가장 높았으며 졸참나무, 굴거리나무, 회양목이 주요 isoprnen 방출 수종으로 나타났다. Monoterpene 방출량은 리기다소나무에서 가장 높았으며 고로쇠, 일본잎갈나무, 백목련, 메타세쿼이아, 잣나무, 소나무, 전나무가 주요 monpterpene 방출 수종으로 나타났다. Monotrerpene 주요 물질은 α-pinene, myrcene, limonene, β-pinen, sabinene이였으며, sesquiterpene의 주요 물질은 caryophyllene, farnesene으로 나타났다. Oxygenated monoterpene의 주요 물질은 pulegone, borneol, menthol, eucalyptol, nerol이였고 oxygenated sesquiterpene에서는 carypphyllene oxide가 주요 물질로 검출되었지만 30개 수종에서 sesquiterpene과 oxygenated sesquiterpene의 방출량은 상대적으로 낮았다.