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오좌섭,지옥표,문형인,Oh, Joa-Sub,Zee, Ok-Pyo,Moon, Hyung-In 한국생약학회 2000 생약학회지 Vol.31 No.4
In search for plant-derived cytotoxic compounds, it was found that the $CHCl_3$ and EtOAC extracts obtained from the flowers of Paulownia coreana Uyeki (Scrophulariaceae) exhibited significant cytotoxic activity against human tumor cell lines, A549, SK-OV-3, SK-MEL-2, XF498, and HCT15. Activity-guided fractionation on the basis of the inhibitory activity against the growth of human tumor cell lines, in vitro, and repeated column chromatography afforded several cytotoxic compounds from P. coreana. The structures and stereochemistry of these compounds were established, on the basis of analysis of spectra including IR, UV, EI-MS, $^{1}H-NMR,\;^{13}C-NMR$ and some chemical transformations, as Compound PCCl $(2-hydroxy-4(15),11(13)-eudesmadien-8{\beta},12-olide)$, Compound $PCC2(2,3-dihydro-4-hydroxy-1(15),11(13)-xanthadien-8{\beta},12-olide)$, Compound PCE1 (chrysophanol), Compound PCE2 (emodin), Compound PCE3 (physcion). Cytotoxic activity of compounds obtained from P. coreana. on five tumor cells lines was evaluated by procedure of SRB methods.
율무근의 식물화학적 성분 연구 및 Tyrosinase 저해 활성
최윤혁 ( Yun-hyeok Choi ),최춘환 ( Chun Whan Choi ),이재연 ( Jae Yeon Lee ),안은경 ( Eun-kyung Ahn ),오좌섭 ( Joa Sub Oh ),홍성수 ( Seong Su Hong ) 한국응용생명화학회 2017 Journal of Applied Biological Chemistry (J. Appl. Vol.60 No.1
In the course of screening tyrosinase inhibitory activity, EtOAc-soluble fraction of Coix lachryma-jobi var. mayuen Stapf. (Gramineae) roots showed significant inhibition. Further fractionation of the EtOAc-soluble fraction resulted in six compounds, which were identified as (+)-icariol A<sub>2</sub> (1), zhepiresionol (2), 4-hydroxybenzaldehyde (3), trans-ρ-coumaric acid (4), N-(2- hydroxy-4-methoxyphenyl)-2-hydroxyacetamide (5), and coixol (6). The chemical structures of these compounds were identified on the basis of spectroscopic methods (MS, 1D and 2D NMR) and comparison with literature values. Compound 1 was first reported from this plant. Also, this is the first time that the isolation of compound 5 has been reported from nature source. Among the isolated compounds, compounds 4 and 6 showed enzyme inhibitory activity, with IC<sub>50</sub> values of 6.5 and 62.4 μM, respectively, in comparison with these of positive control, arbutin.
3T3-L1 지방전구세포에서 용아초 에틸아세테이트 추출물의 항비만 효과
이정아(Jung A Lee),안은경(Eun-Kyung Ahn),홍성수(Seong Su Hong),오좌섭(Joa Sub Oh) 한국식품영양과학회 2012 한국식품영양과학회지 Vol.41 No.2
본 연구에서는 3T3-L1 지방전구세포를 이용하여 용아초 에틸아세테이트 추출물의 항비만 활성을 확인하고자 하였다. 용아초 에틸아세테이트 추출물에 의한 지방세포 분화 및 adipogenesis 저해 활성을 확인하기 위해 추출물을 3T3-L1 지방전구세포에 분화를 유도하면서 농도별(50, 100 μg/mL)로 처리하였고, 그 결과 용아초 에틸아세테이트 추출물은 지방세포의 분화를 억제시켰다. 이 같은 활성에 대한 기전을 확인하기 위해 PPARγ 전사활성과 지방세포 분화에 관여하는 유전자들의 활성을 확인해 보았다. 실험 결과 용아초 에틸아세테이트 추출물은 PPARγ 전사 활성을 억제시켰고 PPARγ 및 C/EBPα의 mRNA 발현을 농도 의존적으로 감소시켰으며 지방세포 분화에 관여하는 adipokine들의 발현을 조절하는 것으로 나타났다. 따라서 용아초 에틸아세테이트 추출물의 항비만 효과는 지방 생성의 주요 전사인자인 PPARγ와 C/EBPα의 유전자 발현조절을 통해 지방 분화억제 및 지방 축적을 효과적으로 감소시키는 것으로 보이며, 효과가 있는 농도가 100 μg/mL로 천연물질로써 비교적 낮은 농도에서 효과가 나타나는 것으로 보아 항비만 소재로의 개발 가능성이 있을 것으로 사료된다. To evaluate the anti-obesity effect of Agrimonia pilosa L., this study investigated that ethyl acetate extract from A. pilosa L. (EAAP) suppresses lipid accumulation and inhibits expression of adipogenic marker genes, such as peroxisome proliferator activated receptor γ (PPARγ), CCAAT-enhancer-binding protein α (C/EBPα), glucose transporter 4 (GLUT4), and adiponectin in 3T3-L1 preadipocytes. We demonstrated that EAAP inhibited adipocyte differentiation and expression of PPARγ and C/EBPα mRNA levels in a dose-dependent manner. In addition, EAAP reduced the PPARγ transcriptional activity stimulated by rosiglitazone in HEK 293T cells and decreased the expression of GLUT4 and adiponectin in 3T3-L1 cells. These results suggest that EAAP inhibits preadipocyte differentiation and adipogenesis by blocking of PPARγ and C/EBPα gene expression in 3T3-L1 cells.
권진관(Jin Gwan Kwon),서찬곤(Changon Seo),홍성수(Seong Su Hong),서동완(Dong-Wan Seo),오좌섭(Joa Sub Oh),김진규(Jin Kyu Kim) 한국식품영양과학회 2016 한국식품영양과학회지 Vol.45 No.11
본 연구는 HPLC를 이용하여 닥나무 추출물을 건강기능식품 원료로 개발하기 위하여 지표성분인 marmesin의 분석법설정과 분석법에 대한 검증을 하고자 하였다. 표준액과 닥나무 추출물은 다른 물질의 간섭 없이 분리되었으며, 표준액과 추출물의 피크 유지시간이 일치한 spectrum을 나타내었다. 또한, blank에서 표준액과 겹치는 피크가 없는 것으로 특이성을 확인하였다. 검량선의 상관계수(R²)는 0.9999로 모두 양호한 직선성을 보였으며, 직선상의 검출한계는 2.8~6.2μg/mL였고 정량한계는 8.4~18.6 μg/mL로 나타났다. 닥나무 추출물 1.3, 2.6, 3.9 mg/mL의 세 농도의 회수율은 100.35~101.18%였으며 정밀도는 0.27~0.30%로 나타나 정밀도 2.0% 이하로서 정확성이 있음을 알 수 있었다. 정밀성은 0.04~0.30%의 정밀도를, 실험실 내 정밀성에서는 0.03~0.30%의 정밀도를 나타내었고 intra-day에서의 정밀도는 0.25~0.42%, inter-day에서는 0.32~0.70%의 정밀도를 나타내어 닥나무 추출물의 지표성분 marmesin의 분석법은 적합한 시험법임이 검증되었다. 본 분석법은 닥나무 추출물의 건강기능식품 원료 개발을 위한 기초자료로 활용될 것으로 생각한다. An HPLC analysis method was developed for standard determination of marmesin as a functional health material in Broussonetia kazinoki extract. HPLC was performed on a C18 Kromasil column (4.6×250 mm, 5 μm) with a gradient elution of 0.1% (v/v) trifluoroacetic acid and acetonitrile at a flow rate of 1.0 mL/min at 30°C. The analyte was detected at 330 nm. The HPLC method was validated in accordance with International Conference on Harmonization guidelines for analytical procedures with respect to specificity, precision, accuracy, and linearity. The limit of detection and quantitation were 6.2 and 18.6 μg/mL, respectively. Calibration curves showed good linearity (r²>0.9999), and the precision of analysis was satisfactory (less than 0.3%). Recoveries of quantified compound ranged from 100.35 to 101.18%. This result indicates that the established HPLC method is very useful for the determination of marker compounds in B. kazinoki extracts.
건강기능식품 기능성 원료로서 곰취잎 추출물의 Caffeoylquinic Acid계 성분 분석법 검증
권진관(Jin Gwan Kwon),김진규(Jin Kyu Kim),서찬곤(Changon Seo),홍성수(Seong Su Hong),안은경(Eun-Kyung Ahn),서동완(Dong-Wan Seo),오좌섭(Joa Sub Oh) 한국식품영양과학회 2016 한국식품영양과학회지 Vol.45 No.1
본 연구는 HPLC를 이용해 개별 인정형 건강기능식품 원료로 개발하기 위하여 곰취잎 추출물의 지표성분인 CA, 3,4-DCQA, 3,5-DCQA 및 4,5-DCQA의 동시분석법 설정과 분석법에 대한 검증을 실시하고자 하였다. 그 검증의 결과 표준액과 곰취잎 추출물의 HPLC 크로마토그램을 비교하여 피크가 분리됨을 확인하고 다른 물질의 간섭 없이 분리되었으며, 표준액의 피크 유지시간과 추출물의 피크 유지시간이 일치하였고 동일한 spectrum을 나타내었다. 또한 blank에서 표준액과 겹치는 피크가 없는 것으로 특이성을 확인하였다. 검량선의 상관계수는 CA, 3,4-DCQA, 3,5-DCQA 및 4,5-DCQA 각각 0.9999, 0.9999, 0.9999 및 0.9999로 모두 양호한 직선성을 보였으며, 직선상의 검출한계는 3.0~13.2 μg/mL였으며 정량한계는 9.2~39.8 μg/mL로 나타났다. 곰취 추출물 0.6, 1.2 및 1.8 mg/mL의 세 농도의 회수율은 98.96~101.81%였으며 RSD는 0.14~0.89%로 나타나 RSD 2.0% 이하로서 정확성이 있음을 알 수 있었다. 정밀성은 0.04~0.51%의 정밀도를, 실험실 내 정밀성에서는 0.02 ~0.90%의 정밀도를 나타내었고 intra-day에서의 정밀도는 0.07~0.63%, inter-day에서는 0.39~0.66%의 정밀도를 나타내어 곰취잎 추출물의 지표성분 CA, 3,4-DCQA, 3,5-DCQA 및 4,5-DCQA의 분석법은 적합한 시험법임이 검증되었다. 본 분석법이 곰취 추출물 개별 인정형 건강기능식품원료 개발을 위한 기초자료로 활용될 것으로 사료된다. An HPLC analysis method was developed for standard determinations of chlorogenic acid, 3,4-di-O-caffeoylquinic acid, 3,5-di-O-caffeoylquinic acid, and 4,5-di-O-caffeoylquinic acid as functional health materials in Ligularia fischeri extract. HPLC was performed on a C18 Kromasil column (4.6×250 mm, 5 μm column) with a gradient elution of 0.1% (v/v) trifluoroacetic acid and acetonitrile at a flow rate of 1.0 mL/min at 30°C. The analytes were detected at 330 nm. The HPLC method was validated in accordance with the International Conference on Harmonization guideline of analytical procedures with respect to specificity, precision, accuracy, and linearity. The limits of detection and quantitation for the four compounds were 3.0∼14.6 and 9.2∼44.4 μg/mL, respectively. Calibration curves showed good linearity (r²>0.999), and the precision of analysis was satisfied (less than 0.9%). Recoveries of quantified compounds ranged from 98.96 to 101.81%. This result indicates that the established HPLC method is very useful for the determination of marker compounds in Ligularia fischeri leaf extracts.
Balb/c 마우스에서 초과 추출물의 3주간 반복 경구투여 독성평가
박주형 ( Ju Hyeong Park ),조영락 ( Young Rak Cho ),고혜진 ( Hye Jin Ko ),정원식 ( Wonsik Jeong ),안은경 ( Eun Kyung Ahn ),오준호 ( Junho Oh ),오좌섭 ( Joa Sub Oh ) 한국응용생명화학회 2015 Journal of Applied Biological Chemistry (J. Appl. Vol.58 No.2
Abstract In the present study, we investigated the oral toxicity of Amomum tsao-ko Crevost et Lemaire, (Zingiberaceae) extract in Balb/c mice (BALB, n=60) for 3 weeks. Balb/c mice (10 mice/ group, 6 group, 20±2 g, 6 weeks) were orally administered for 21 days, with dosage of 250, 500, 1000, 2000 mg/kg/day. Ethanolextract of A. tsao-ko did not affect any significant change of mortality, clinical signs, organs and body weights. Also, there were not significantly difference from the naive group (control) in hematological and serum biochemical examination. Consequently, these findings indicate that 3-week treatment with the ethanol extract of A. tsao-ko was not any toxic effects in Balb/c mice and the no-observed adverse effect level (NOAEL) for oral toxicity was determined to be 2000 mg/kg/day under our experimental conditions.
홍성수 ( Seong Su Hong ),최윤혁 ( Yun Hyeok Choi ),서화진 ( Hwa Jin Suh ),강민정 ( Min Jung Kang ),신정혜 ( Jung Hye Shin ),권오운 ( Oh Oun Kwon ),오좌섭 ( Joa Sub Oh ) 한국응용생명화학회 2015 Journal of Applied Biological Chemistry (J. Appl. Vol.58 No.2
Ten compounds were isolated from the ethanolic extract of the leaves of Acacia catechu (Fabaceae), and their structures were identified as nine flavonoids [(+)-catechin (1), (-)- epicatechin (2), (+)-afzelechin (3), (-)-epiafzelechin (4), (+)- mesquitol (5), kaempferol (6), quercetin (7), quercetin 3-methyl ether (8), and caryatin (9)] and an ellagic acid (10). The chemical structures of these compounds were identified on the basis of spectroscopic methods (mass spectrometry, 1D and 2D nuclear magnetic resonance) and comparison with literature values. This is the first time that the isolation of caryatin (9) has been reported from Acacia genus.
초과(草果)의 RBL-2H3 세포 항원 유도 탈과립 억제성분
정원식 ( Wonsik Jeong ),홍성수 ( Seong Su Hong ),박선미 ( Sun-mi Park ),이정아 ( Jung A Lee ),박주형 ( Ju-hyoung Park ),안은경 ( Eun-kyung Ahn ),최춘환 ( Chun Whan Choi ),오좌섭 ( Joa Sub Oh ) 한국응용생명화학회 2021 Journal of Applied Biological Chemistry (J. Appl. Vol.64 No.1
Bioactivity-guided fractionation of EtOH extract of the dried fruits of Amomum tsao-ko led to isolation of three compounds (1-3). Their structures were elucidated by spectroscopic methods (MS, 1D and 2D-NMR) and comparison with literature values, as naringenin-5-O-methyl ether (1), helichrysetin (2), and cardamomin (3). Compound 2 was obtained from the genus Amomum for the first time. Among them, compounds 2 and 3 inhibited on the release of β-hexosaminidase from RBL-2H3 cells, with 99.1 and 21.3% at the concentration of 50 μM, respectively.