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7-티아지닐 세파로스포린 유도체의 합성과 생리활성에 관한 연구
이영행(Young Haeng Lee),채규윤(Kyu Yun Chai),황선암(Sun Am Hyang),최원식(Won Sik Choi) 대한약학회 1997 약학회지 Vol.41 No.4
New cephalosporin antibiotics, 7-[(3,4-dihydro-6-methoxycarbonyl-2,2-dimethyl-2H-1,4-thiazin-3-yl)acetamido]-3-substituted-3-cephem-4-carboxylic acid derivatives 2a-2d, 7-[(3,4-dihydro-6-ethoxycarbonyl-2,2-dimethyl-2H-1,4-thiazin-3-yl)acetamido] -3-substituted-3-cephem-4-carboxylic acid derivatives 3a-3d and 7-[(3,4-dihydro-6-methoxycarbonyl-2,2-dimethyl-2H-1,4-thiazin-3-yl-1-(S)-oxide)acetamido]-3-substituted-3-cephem-4-carboxylic acid derivatives 4a-4d were synthesized. Antibacterial activities of these new cephalosporin derivatives and the relationship between their structures and their activities were examined. Among them, 7-[(3,4-dihydro-6-methoxycaronyl-2,2-dimethyl-2H-1,4-thiazin-3-yl-1-(S)oxide)-acetamido]-3-[(1,2,3-triazol-5-yl)thiomethyl]-3-cephem-4-carboxylic acid 4d exhibited the antibacterial activities against Gram(+)and Gram(-) bacteria.
A Study on the Usefulness of 3D Imaging in Micro-CT for Observing the Microstructure of Mice
이상호,이종석,임청환,정홍량,채규윤,한범휘,한상현,홍동희,한태종,박성훈,모은희,전홍영,Lee, Sang-Ho,Lee, Jong-Seok,Lim, Cheong-Hwan,Jung, Hong-Ryang,Chai, Kyu-Yun,Han, Beom-Hee,Han, Sang-Hyun,Hong, Dong-Hee,Han, Tae-Jong,Park, Sung-Hoon,Mo The Society of Digital Policy and Management 2014 디지털융복합연구 Vol.12 No.3
본 연구는 실시간 동적영상(Real-time dynamic image)을 획득할 수 있는 고해상도 엑스선 영상장치인 마이크로 CT 을 이용하여 흰쥐의 미세 혈관구조를 관찰함은 물론 국내 원광 방사선영상 과학연구 센터에서 개발한 마이크로 CT 에 대한 유용성을 알아보고자 한다. 흰쥐 몸 전체의 2D 영상을 얻은 후 MIP(maximum intensity projection), VRT(volume rendering technique)기법을 이용하여 혈관구조의 조영된 3D 영상을 얻을 수 있었고 이 3D 혈관 영상을 머리, 복부, 심장과 몸 전체의 혈관시스템으로 각각 분류하였다. In this thesis we observe microvascular structure in mice by using micro-computed tomography (CT), which is high-resolution X-ray imaging equipment that can acquire Real-time dynamic image, and it aims to investigate the usefulness of micro-CT developed by Institute for Radiological Imaging Science Wonkwang University School of Medicine. After acquiring the systemic images of rats, contrast-enhanced 3D images of vascular structures could be acquired by using Maximum Intensity Projection (MIP) and Volume Rending Technique (VRT), This was divided into each vascular system of head, abdomen and heart and systemic vascular system.
정공피 추출물의 (1,3)$\beta$-Glucan Synthase에 대한 억제효과
유명자,김보미,이정호,이영행,채규윤,백승화,You, Myung-Ja,Kim, Bo-Mi,Lee, Jeong-Ho,Lee, Young-Hang,Chai, Kyu-Yun,Baek, Seung-Hwa 대한동의생리학회 2008 동의생리병리학회지 Vol.22 No.5
A examination of the kinetic properties of UDP-glucose : (1,3)-$\beta$-glucan (callose) synthase from mung bean seedings (Sorbus cortex) shows that these enzymes have a complex interaction with UDP-glucose and various effectors. Deoxynojirimycin increased the inhibitory effect of (1,3)-$\beta$-glucan synthase at the concentration-dependent manner by fluorescence assay. The inhibitory effect of Fr. 2-16 (97.15%) showed higher than that of deoxynojirimycin (80.63%). Fr. 2-3 inhibited the growth of the Candida albicans at 1 mm inhibition zone by disk diffusion method. These results suggest that Sorbus cortex extract can be used as a stable antifungal material.
1-Benzyl-4-Iodomethyl-2-Azetidinone의 합성과 Iodo기에 대한 전기화학적 환원반응
김일광,이영행,이채호,채규윤,김윤근,Kim Il Kwang,Lee Young Haeng,Lee Chai Ho,Chai Kyu Yun,Kim Yoon Geun 대한화학회 1991 대한화학회지 Vol.35 No.1
1-Benzyl-4-iodomethyl-2-azetidinone(BIMA)을 합성하여 iodomethyl기에 대한 전기화학적 환원을 direct current, differential pulse polarography, cyclic voltammetry 그리고 controlled potential coulometry 방법으로 연구하였다. BIMA의 환원과정은 1단계(-1.35 volts vs. Ag-AgCl)에서 완전비가역과 2전자이동후에 양성자가 첨가되는 EEC 반응기구로 진행되었으며 1-benzyl-4-methyl-2-azetidinone이 생성되었다. 양이온 계면활성제(cetyltrimethylammonium bromide)의 농도가 진하여질수록 양전위 이동이 있었으나 음이온 계면활성제(sodium lauryl sulfate)의 경우에는 2단계로 세분화되는 현상이 나타났다. pH변화에 따른 전극환원과정과 생성물 분석의 결과를 바탕으로 전기화학적 반응기구를 제안하였다. 1-Benzyl-4-iodomethyl-2-azetidinone(BIMA) was synthesized and its electrochemical reduction was investigated by direct current, differential pulse polarography, cyclic voltammetry and controlled potential coulometry. The irreversible two electron transfer on reductive dehalogenation of iodo group proceeded to form 1-benzyl-4-methyl-2-azetidinone by EEC electrode reaction mechanism at the first reduction step(-1.35 volts vs. Ag-AgCl). The polarographic reduction waves separated into two reduction steps due to anionic surfactant (sodium lauryl sulfate) effects, while the waves were shifted to the positive potential as the concentration of cationic surfactant (cetyltrimethylammonium bromide) increased. Upon the basis of results on the product analysis and interpretation of polarogram with pH variable, EEC electrochemical reaction mechanism was suggested.
${\alpha},{\beta}$-Dibenzyl N-Benzylidene L-Aspartate 의 Imino 기에 대한 선택적 전해환원반응
김일광,김윤근,이영행,채규윤,Kim, Il-Kwang,Kim, Youn-Geun,Lee, Young-Haeng,Chai, Kyu-Yun 대한화학회 1989 대한화학회지 Vol.33 No.6
0.1M LiCl의 ethanol 용액에서 ${\alpha},{\beta}$-dibenzyl N-benzylidene L-aspartate의 전기화학적 환원을 direct current, differential pulse polarography, cyclic voltammetry 그리고 controlled potential coulometry 방법으로 연구하였다. ${\alpha},{\beta}$-dibenzyl N-benzylidene L-aspartate의 환원과정은 1단계(-0.92 volts vs. Ag-AgCl)에서 양성자 첨가와 2전자이동에 의한 완전 비가역의 CEC 혹은 CE 반응기구로 진행되었으며 ${\alpha},{\beta}$-dibenzyl N-benzyl L-aspartate가 생성되었다. 계면활성제가 포함된 용액에서 polarography 환원파는 전체적으로 약간 억제되었으며 Triton X-100의 농도가 진해질수록 비가역성을 증가시키는 것으로 나타났다. 생성물 분석과 pH 변화에 따른 전극환원과정에 대한 고찰로 전기화학적 반응기구를 제안하였다. The electrochemical reduction of ${\alpha},{\beta}$-dibenzyl N-benzylidene L-aspartate in 0.1M LiCl ethanol solution was investigated by direct current (DC), differential pulse (DP) polarography, cyclic voltammetry and controlled potential coulometry(CPC). The irreversible reductive amination of imino group proceeded to form ${\alpha},{\beta}$-dibenyl N-benzyl L-aspartate by CEC or CE electrochemical reaction mechanism at the first reduction step (-0.92 volts vs. Ag-AgCl). The polarographic reduction wave was slightly suppressed due to inhibitory effect of micelle, while the irreversibility was increased according to the increase of Triton X-100 concentration. Upon the basis of product analysis and polarogram interpretation with pH change, possible CE electrode reaction mechanism was suggested.
L1210 및 $P388D_1$ 세포에 대한 고삼 에틸 아세테이트 추출물의 세포독성에 관한 연구 (III)
류홍선,신민교,양은영,조훈,채규윤,강길웅,백승화,Ryu, Hong-Sun,Shin, Min-Kyo,Yang, Eun-Yeong,Cho, Hoon,Chai, Kyu-Yun,Kang, Kil-Ung,Baek, Seung-Hwa 한국생약학회 2000 생약학회지 Vol.31 No.1
This study was carried out to evaluate cytotoxic effects of the roots of Sophora flavescens Ait. extracts on murine leukemia tumor cells lines $(P388D_1\;and\;L1210)$. Disruptions in cell organelles were determined by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay. The comparison of $IC_{50}$ values of the ethyl acetate of Sophora flavescens Ait. extract in leukemia cell lines showed that their susceptibility to these extracts decreased in the following order : Adriamycin>Fr.4>Fr.5>Fr.3>Fr.1>Fr.2 by the MTT assay. These results suggest that the fraction 4 of the ethyl acetate soluble extract of Sophora flavescens Ait. may be a valuable choice for the studies on the treatment of murine leukemia cell lines.
김보미,김의성,이영행,유병수,채규윤,Kim, Bo-Mi,Kim, Eui-Sung,Lee, Young-Hang,Yu, Byung-Soo,Chai, Kyu-Yun 대한한의학방제학회 2010 大韓韓醫學方劑學會誌 Vol.18 No.2
The Geranium nepalense has been used traditionally for treatment of various diseases. However, the molecular studies on the effect of Geranium nepalense have not been carried out. In the present study, Quercetin, quercitrin, and afzelin were isolated from the methanol extract of Geranium nepalense were tested for their anti-inflammatory effect. The anti-inflammatory effect of the compounds was studied in lipopolysaccharide(lps)-treated mouse macrophage cells, RAW 264.7. RAW 264.7 cells were pre-incubated with isolated compounds(0, 5, 10, 20, 40, $50\;{\mu}g/ml$) for 4h and treated with $1\;{\mu}g/ml$ lps for 18h, and then the anti-inflammatory effects of compounds were determined. The results are as follows: Quercetin at various concentration inhibited the viability of Raw 264.7 from 7% to 45%, quercitrin from 25% to 80%, and afzelin from 13% to 52%. Isolated compounds showed a significant decrease in iNOS (inducible nitric oxide synthase) and COX-2 (cyclooxygenase-2). These results suggest that these compounds can be used as stable anti-inflammatory materials.
윤용갑(Young Gab Yun),채규윤(Kyu Yun Chai),록란잔밭(Kyung Kwan Lee),이경관(Lok Ranjan Bhatt),백승화(Seung Hwa Baek) 대한약학회 2009 약학회지 Vol.53 No.6
Sakuranetin, prunetin and dihydroquercetin were isolated from the methanol extract of Sorbus commixta by 1D/2D-NMR and LC-MASS spectrometry. Medicating these compounds to RAW264.7 cell that was pre-treated by lipopolysaccharide revealed anti-inflammatory effects that greatly inhibited the production of NO (nitric oxide) and PEG2 (prostaglandin E2), which are well known to cause the expression of iNOS (inducible nitric oxide synthase) and COX-2 (Cyclooxygenase-2). These results suggest that these compounds can be used as stable anti-inflammatory materials.
김보미,유명자,송미선,권태오,이영행,채규윤,Kim, Bo-Mi,Yoo, Myung-Ja,Song, Mi-Seon,Kwon, Tae-Oh,Lee, Young-Hang,Chai, Kyu-Yun 대한한의학방제학회 2011 大韓韓醫學方劑學會誌 Vol.19 No.2
Objectives : The Lycoris squamigera Maxim has been used traditionally for treatment of various diseases. However, the studies on the effect of Lycoris squamigera Maxim have not been carried out. In the present study, extract of Lycoris squamigera Maxim were tested for their anti-inflammatory and anti-oxidation effect. Methods : The anti-inflammatory effect of the various solvent extract was studied in lipopolysaccharide (lps)-treated mouse macrophage cells. RAW 264.7 cells were pre-incubated with Lycoris squamigera Maxim extracts for 4h and treated with $1\;{\mu}g/m{\ell}$ lps for 18h, and then the anti-inflammatory effects of extracts were determined. The anti-oxidation effect of extracts measured by DPPH method, reductive potential test, total phenolics test. Results : Extracted root's ethyl acetate layer showed a significant decrease in nitric oxide. And that layer (root's ethyl acetate extract) was showed decrease in TNF-${\alpha}$ concentration dependently. Separated from Root's ethyl acetate extract was fraction 1 has $0.1{\sim}5\;{\mu}M$ range, fraction 2 has $0.1{\sim}10\;{\mu}M$ range did not showed cytotoxicity. Anti-oxidation result as DPPH test showed the best was root ethyl acetate extract. Redusing power was made a comparison between fractions and standard. They were showed similar value. Fraction's total phenol containing result was better then standard. Conclusions : These results suggest that these extracts can be used as anti-inflammatory, anti-axidation materials.