• Natural Product Sciences
• /
• 제6권2호
• /
• pp.79-81
• /
• 2000

Investigation of the fruits of Chaenomeles sinensis (Rosaceae) resulted in the isolation of a minor flavonoid. The structure of flavanone glycoside was determined to be as $2-hydroxynaringenin-7-O-{\beta}-glucoside$ on the basis of FAB-MS and spectral evidence, especially by 2D-NMR $(^1H-^1H\;COSY,\;HMQC,\;HMBC\;and\;NOESY)$.

• 한국응용약물학회:학술대회논문집
• /
• 한국응용약물학회 2002년도 창립10주년기념 및 국립독성연구원 의약품동등성평가부서 신설기념 국재학술대회:생물학적 동등성과 의약품 개발 전략을 위한 국제심포지움
• /
• pp.247-247
• /
• 2002

• 대한화장품학회지
• /
• 제30권4호
• /
• pp.499-502
• /
• 2004

장미과 식물(에탄을 추출)의 항산화력을 측정하기 위하여 1,1-diphenyl-2-picrylhydrazyl (DPPH) 자유 라디칼 생성 시스템을 이용하여 하였다. 또한 산화 환원 과정을 통하여 피부의 과잉 색소 생성에 관련된 멜라닌 생합성 과정의 조절 가능성을 조사하였다. 장미과 식물중에서 Prunus sargentii, Rubus coreanus, Chaenomeles sinensis, Photinia glabra와 Pyrus pyrifolia은 생합성 과정에서 dopa [3-(3,4-dihydroxyphenyl) alanine]를 도파크롬으로 변환시켜 주는 tyrosinase 저해 효과를 나타내었다. MTT 실험법은 장미과 에탄올 추출물의 사람 섬유아세포에 미치는 독성정도를 실험하기 위해 사용되었다. 장미과 식물중 특히 Prunus sargentii의 껍질, Phorinia glabra의 껍질과 나무 그리고 Chaenomeles sinenis의 잎, 껍질, 나무 모든 부분에서 mushroom tyrosinase에 대해 $100{\;}{\mu}g/mL$에서 50\%$ 이상의 저해 활성을 보였으며, $10{\;}{\mu}g/mL$ 농도에서 강한 라디칼 소거 효과를 나타내었다. 또한 이들 추출물은 사람 섬유아 세포에 대해 높은 생존율을 나타냄으로써 멜라닌 형성 과정을 조절할 수 있을 것으로 기대한다.

• 생약학회지
• /
• 제20권1호
• /
• pp.10-12
• /
• 1989

Chromatographic separation of the hexane-soluble part and chloroform fraction from the fruits of Chaenomeles sinensis Koehne resulted in the isolation of compound 1 and 2, which were characterized as ${\beta}-sitosterol$ and oleanolic acid by chemical and spectral analysis, respectively.

• 한국응용약물학회:학술대회논문집
• /
• 한국응용약물학회 2002년도 창립10주년기념 및 국립독성연구원 의약품동등성평가부서 신설기념 국재학술대회:생물학적 동등성과 의약품 개발 전략을 위한 국제심포지움
• /
• pp.246-246
• /
• 2002

• 생약학회지
• /
• 제42권3호
• /
• pp.223-228
• /
• 2011

Chaenomeles sinensis Koehne (Rosaceae) is a deciduous tree and is distributed in China, Korea and Japan. In previous studies on the fruits of C. sinensis, some triterpenoid compouds such as oleanolic acid, tormentic acid were reported. In an ongoing investigation into biologically active compounds from natural products, the methanol extract of the stems of C. sinensis was investigated. By means of the repeated column chromatography using silica gel, Sephadex LH-20, LiChroprep RP-18, betulin (1), tormentic acid (2), 1-${\beta}$-D-glucopyranosyl-3,4,5-trimethoxybenzene (3), lyoniresinol-2a-O-${\alpha}$-L-rhamnopyranoside (4) were isolated. The chemical structures of compounds 1-4 were determined by the basis of physico-chemical properties and spectroscopic methods such as 1D and 2D NMR. For the isolated compounds (1-4), the inhibitory activity of IL-6 production in TNF-${\alpha}$ stimulated MG-63 cell was examined. Among the isolates, betulin (1), 1-${\beta}$-D-glucopyranosyl-3,4,5-trimethoxybenzene (3), lyoniresinol-2a-O-${\alpha}$-L-rhamnopyranoside (4) showed inhibitory effects on IL-6 production in TNF-${\alpha}$ stimulated MG-63 cell.

• 약학회지
• /
• 제39권6호
• /
• pp.610-615
• /
• 1995

Three acidic triterpense were isolated from the ethyl acetate soluble fraction of the fruits of Chenomeles sinensis (Rosaceae) together with previously reported oleanolic acid and ursolic acid by repeated silica gel colunm chromatography. Their structures have been elucidated as $2{\alpha},{\;}3{\betha}-dihydroxyolean-l2-en-28-oic$ acid(l. maslinic acid), $2{\alpha},{\;}3{\alpha},{\;}19{\alpha}-trihydroxy-urs-12-en-28-oic$ acid (2, euscaphic acid), and $2{\alpha},{\;}3{\betha}-dihydroxyolean-l2-en-28-oic$ acid (3,tormentic acid), respectively, on the basis of chemical and spectral evidence.

• 한국균학회지
• /
• 제44권4호
• /
• pp.342-345
• /
• 2016

모과나무 가지의 일부에서 이상 증상이 있는 부위로부터 균을 순수분리하여 균류에 대한 형태적 특성과 더불어 ${\beta}$-tubulin 유전자 염기서열에 기반한 계통학적 분석을 수행하였다. 동정된 균은 점균류에 속하는 Stemonaria longa로 확인되었으며 국내 미기록 종임을 확인하였다.

• 생약학회지
• /
• 제49권1호
• /
• pp.40-46
• /
• 2018

Chaenomeles sinensis (Thouin) Koehne fruit (Rosaceae) has been used as a traditional medicine in Korea, Japan and China to treat sore throat, diarrhea and inflammation. The ethanol extract of C. sinensis fruit was successively partitioned as methylene chloride, ethyl acetate, n-butanol and $H_2O$ soluble fractions. Among those fractions, the n-butanol fraction showed the most potent DPPH radical scavenging and superoxide quenching activities. To verify antioxidant activities, the n-butanol fraction was checked the activities of superoxide dismutase (SOD) and catalase activities, and intracellular ROS levels and oxidative stress tolerance in Caenorhabditis elegans. Furthermore, to see if increased stress tolerance of worms by treating of the n-butanol fraction was due to regulation of stress-response gene, we quantified SOD-3 expression using transgenic strain. Consequently, the n-butanol fraction elevated SOD and catalase activities of C. elegans, and reduced intracellular ROS accumulation in a dose-dependent manner. Moreover, the n-butanol fraction-treated CF1553 worms exhibited significantly higher SOD-3::GFP intensity.

• Archives of Pharmacal Research
• /
• 제25권6호
• /
• pp.842-850
• /
• 2002

Tissue factor (TF, tissue thromboplastin or coagulation factor III) accelerates the blood clotting, activating both the intrinsic and the extrinsic pathways to serve as a cofactor. In order to isolate TF inhibitors from the fruits of Chaenomeles sinensis, an activity-guided purification utilizing a bio-assay method of prothrombin time prolongation, was carried out to yield five active flavoniods such as hovetrichoside C (1) ($IC_{50}$ = 14.0 $\mu$g), luteolin-7-Ο-$\beta$-D-glucuronide (3) ($IC_{50}$ = 31.9$\mu$g), hyperin (4) ($IC_{50}$ = 20.8 $\mu$g), avicularin (6) ($IC_{50}$ = 54.8 $\mu$g) and quercitrin (10) ($IC_{50}$ = 135.7 $\mu$g), along with other inactive compounds such as ($\pm$)-(2E,4E)-Ο-$\beta$-D-glucopyranosyl-4'-hydroxy-$\beta$-ionylideneacetic acid ester (2), genistein-7-Ο-$\beta$-D-glucopyranoside (5), luteolin-3'-methoxy-4'-Ο-$\beta$-D-glucopyranoside (7), luteolin-7-Ο-$\beta$-D-glucuronide methyl ester (8), tricetin-3'-methoxy-4'-Ο-$\beta$-D-glucopyranoside (selagin-4'-Ο-$\beta$-D-glucopyranoside) (9), (-)-epicatechin (11), luteolin-4'-Ο-$\beta$-D-glucopyranoside (12) and apigenin-7-Ο-$\beta$-D-glucuronide methyl ester (13). The structures of the isolated compounds were elucidated through spectral analysis. Among them, compounds 1 to 9, 12 and 13 were isolated for the first time from the fruits of this plant and the compound 9 is a new flavonoid.