• 한국생산제조학회지
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• 제22권1호
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• pp.119-124
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• 2013

In this paper, we analysed fatty acid methyl ester contents in the biodiesel which is produced from the newly developed biodiesel production equipment. The lard oil was used as the raw material through various experimental conditions. Thirty one experiments were conducted, which were based on the experimental conditions that designed by central composite design method. The effects of four independent variables, including reaction temperature, reaction time, oil to methanol molar ratio, and catalytic amount, were investigated at five levels using central composite design (CCD). Fatty acid methyl ester content was chosen dependent variable. Although the results of analysis of the surface with an irregular surface geometry showed that the biodiesel was partially impure after the reaction due to the natural characteristics of the lard oil as the raw material, we could confirm the relationship between them from the facts that the production amount of fatty acid methyl ester changes according to reaction temperature, reaction time, oil to methanol molar ratio, and catalytic amount.

• 한국미생물·생명공학회지
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• 제29권3호
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• pp.149-154
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• 2001

버섯유래 저분자 대사산물을 탐색하던 중 대전근교에서 채집한 젖비단 그물버섯(Suillus granulatus)으로 부터 9종의 화합물을 분리하였다. 젖비단 그물버섯을 메탄올로 추출한 후 용매분획하여 그 중 대산산물이 많이 함유된 chloro-form 층 및 ethyl acetate층 에 대하여 각각 silica gel 및 Sephadx LH-20 column chromatography를 수행하였다. 주요대사산물을 함유하고 있는 분획물을 TLC및 분취용 HPLC를 사용하여 정제한 결과 9종의 화합물을 분리하였다. 분리된 화합물의 화학구조를 규명하기 위하여 NMR 및 mass 분석을 수행하여쓰며 그 결과 이들의 화합물은 4-hydro-xyphenylacetic acid, 4-hydroxybenzaldhyde, 2, 5-dihydro-xybenzoic acid methyl ester, 5-deoxy-5 methylthioadeno- sine. indole 3-carboxlic methyl ester indole-3-carbox-aldehyde 1,3,5-trihydroxy 7-methylanthraquinone nicotinamide, 3-geranylgeranyl-4-hydroxybenzoic acid로 동정하였다.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2006년도 추계학술대회
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• pp.541-543
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• 2006

The feasibility of biodiesel production from soapstock by acid catalyst was tested. The water content of soapstock was more than 40%. Before the esterification of soapstock, the pre-treatment of soapstock was conducted adding potassium hydroxide and sulfuric acid. The pre-treated soapstock contained 99.6wt% of free fatty acid. When the free fatty acid was esterified with methanol, the fatty acid methyl ester content became 91.7wt% under the solid acid catalyst, Amberlyst-15. When this biodiesel was distilled the methyl ester content was 98.1wt% which satisfied the biodiesel Standard. Amberlyst-15 could be recovered easily because it was the soliid catalyst. When sulfuric acid was used as the acid catalyst, the fatty acid methyl ester content was 91.0wt%. From the results, it was possible to produce biodiesel efficiently from soapstock after pre-treatment. Because soapstock is very cheap, it will become good feedstock for biodiesel product ion.

• Journal of Microbiology and Biotechnology
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• 제11권2호
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• pp.329-332
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• 2001

It has been known that, in enzymatic synthesis of cephalexin, the conversion yield was reduced by high loading of ampicillin acylase. In order to elucidate this phenomena, pH-controlled synthesis of cephalexin was examined using a purified Acetobacter turbidans acylase. When the pH of the reaction mixture was maintained at $6.20{\pm}0.04$, the reduction of the maximal conversion rate was not observed even with high enzyme loading. The kinetic parameters also suggest that pH drop during the enzymatic synthesis of cephalexin was mainly attributed to the rapid hydrolysis of D-${\alpha}$-phenylglycine methyl ester to D-${\alpha}$-phenylglycine, rather than the disappearance of 7-amino-3-deacetoxycephalosporanic acid for cephalexin synthesis. At higher molar ratio of two substrates, [D-${\alpha}$-phenylglycine methyl ester]/[7-amino-3-deacetoxycephalosporanic acid], the conversion rate was also elevated under pH-controlled enzymatic synthesis, which implies that the main reason for the pH drop is due to the production of D-${\alpha}$-phenylglycine methyl easter, the effect of a water-methanol cosolvent system on the ester, the effect of a water-methanol cosolvent system on the conversion profile was also examined. Even the though the conversion rate was increased in 10% methanol solution, a higher than 16% methanol in the reaction mixture caused an inactivation of enzyme.

• Bulletin of the Korean Chemical Society
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• 제32권1호
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• pp.169-174
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• 2011

The synthesis of new pyrazolyl and cyclopropyl derivatives of purpurin-18 methyl ester and purpurin-18-N-butylimide 1a, 1b, 2a, 2b and 8 is described. The new compounds were characterized by NMR, UV-vis spectroscopy and mass spectrometry. UV-vis spectra of the new compounds showed long wavelength absorption of ranges 692 - 708 nm ($\lambda_{max}$). Photodynamic effects of the chlorin derivatives 1a, 1b, 2a and 2b were investigated by WST-1 assay in A549 cells, and showed good photodynamic activities with high photocytotoxicity and low cytotoxicity in the dark. In comparison between pyrazolyl and cyclopropyl derivatives, purpurin-18 methyl ester compounds 1a and 1b showed comparable photocytotoxicity result of the cell viabilities, otherwise, pyrazolyl derivative of purpurin-18-N-butylimide 2a showed better cell viabilities than those of cyclopropyl derivative 2b. And cyclopropyl derivative of purpurin-18-N-butylimide 2b showed higher dark cytotoxicity than that of others.

• Biomolecules & Therapeutics
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• 제2권2호
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• pp.136-140
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• 1994

To prove the hypothesis that NO- and N $O_2$-carrying molecules potentiate photorelaxation by generating NO, investigation was carried out using isolated rabbit and human corpus cavernosum. Corporal smooth muscle, in the presence or absence of endothelium, relaxed only slightly upon ultraviolet light (366 nm) irradiation. But, NO-and/or N $O_2$-containing compounds such as streptozotocin and $N^{G}$-nitro-L-arginine methyl ester significantly (p<0.01) enhanced photorelaxation in this tissue. In addition, $N^{G}$-nitro-D-arginine methyl ester, known to lack inhibitory action on NO synthase, showed concentration-dependent potentiation of the photorelaxation. Oxygen radical generating system via copper＋ascorbic acid and guanylate cyclase inhibitor, methylene blue, significantly (p<0.05) inhibited the streptozotocin-potentiated photorelaxation. Nitrite was accumulated by photolysis of streptozotocin, $N^{G}$-nitro-L-arginine methyl ester and $N^{G}$-nitro-D-arginine methyl ester, in a concentration and exposure time dependent manner. These observations indicate that NO is a potent relaxant of rabbit and human corpus cavernosum and further support the hypothesis that NO is released by photolysis from NO- and N $O_2$-carrying molecules.lecules.

• Archives of Pharmacal Research
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• 제26권9호
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• pp.716-718
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• 2003

In the course of our search for Acyl-CoA: cholesterol acyltransferase (ACAT) inhibitors from natural sources, a new type of ACAT inhibitor was isolated from a methanol extract of Diospyros kaki. On the basis of spectral and structural evidence, the compound was identified as pheophorbide A-methyl ester. Pheophorbide A-methyl ester inhibited ACAT activity in a dose dependent manner with an $IC_{50}$ value of 1.85 $\mu$ g/mL.

• 생명과학회지
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• 제14권1호
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• pp.91-97
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• 2004

앞선 연구의 구조적 특성을 근거로 하여, 한 분자내에 MES 유발경련에 작용하는 cyclicimide의 구조를 포함하면, 그들의 구조가 경련 유발 수용체들에 상호 보완적으로 작용, MES및 PTZ유발 경련에 모두 작용할 수 있는 적용 범위가 넓은 항경련성 화합물이 될 수 있을 것으로 생각하여 N-acyl-$\alpha$-aminosuccinimide 1과 N-acyl-$\alpha$-aminoglutar- imide 2 유도체를 합성하였다. 먼저 (R)-2-benzyloxy carbonylamino-succinic acid 3을 출발 물질로 하여 N-acyl-a-aminosuccinimide 1 유도체인 (R)-Benzoic acid 4-benzyloxycarbonyl-amino-2-oxo-pyrrolidin-l-yl ester 6a, (R)4-nitro-benzoic acid 4-benzyloxycarbon-ylamino-2-oxo-pyrrolidin-1-yl ester 6b, (R)-4-nitro-benzoic acid 4-benzyloxycarbonylamino-2-oxo-pyrrolidin-1-yl ester 6c, 그리고 (R)-propionic acid 4-benzyloxycarbonylamino-2-oxo-pyrrolidin-1-yl ester 64를 합성하였다 또한 (R)-3-car-bobenzyloxy-aminoglutarrnic acid 7를 출발물질로 하여 N-acyl-$\alpha$-aminoglutarimide 2유도체인 (R)-(3-Benzyloxycarbonyl-amino-2,6-dioxo-piperidin-1-yloxy)-acetic acid methyl ester 10a, (R)-(3-benzyloxyarbonylamino-2,6-dioxo-piperidin-1-yloxy)-acetic acid ethyl ester l0b, 그리고 (R)-2-(3-benzylox-ycarbonylanino-2,6-dioxo-piperidin-1-yloxy)-propionic acid methyl ester l0c를 합성하였다. 합성된 화합물 6a, 6b, 6c, 6d, 10a, lOb, l0c에 대한 활성평가는 각 단계별 MES test와 PTZ test의 항경련 활성 시험 방법을 가지고 실험할 예정이다.

• 대한약학회:학술대회논문집
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• 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.1
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• pp.135.1-135.1
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• 2003

We have previously reported three new oleanene-type glycosides and kudzusaponin $A_3$ methyl ester and subproside II methyl ester from the roots of Echinosophora koreensis. Further study has now led to the isolation of three known oleanen-type glycosides. sophoraflavoside I, azukisaponin V, and kudzusaponin $SA_3$ as their methyl esters. The structures of theses compounds were characterized by spectroscopic and chemical methods.

• 공업화학
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• 제5권6호
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• pp.1062-1067
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• 1994

Ethylacetoacetate로부터 2단계의 연속합성을 통하여 생성되는 5-methyl-4-imidazolecarboxylic acid ester의 합성반응 속도론과 중간 생성물인 ${\alpha}$, {\beta}$-dioxobutyric acid(일명 diketone)의 반응 안정성을 연구하였다. 반응속도 결정단계는 ${\alpha}$-acetyl-${\alpha}$-hydroxy iminoacetic acid(oxime)로부터 diketone으로 진행되는 과정으로서 반응속도에 영향을 미치는 주된 인자로는 Oxime, HCl의 농도와 반응온도임을 확인하였고 HCl 농도 4.6~8.0M 반응온도 $8.5{\sim}20^{\circ}C$의 변화에 따른 diketone의 최대 반응수율 변화는 50~74%이었다. Power-law 수식모델 및 회분식 반응기 empirical data로부터 diketone 생성반응 속도식을 구하였으며 이 식이 실험 Data와 잘 일치하고 있음을 보였다. 본 연구는 5-methyl-4-imidazolecarboxylic acid ester 연속반응 공정개발의 기초단계로서 반응속도론 연구를 통하여 합성 반응의 특성을 파악하는데 중요한 의의를 두고 있다.