• 대한한방내과학회지
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• 제1권1호
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• pp.64-69
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• 1976

Kami Eui In Tang is being used as a treatment oral medicament on the appendicitis and peritonitis without surgical operation resulting good effect. The component of the medicament are as follow : Coix ma yuen, Paeonia moutan, Patrinia scabiosifolia, Rheum, Coreanum, Cory-dalis nakaii, Trichosanthes kirilowii, Lonicera japonica, Prunus persica, Tarxacum officinale, Author tried to make clear the ant inflammatory effect on rat paw which has become edema formation by carrageenin and detect the active ingredients by thin layer chromatography method. The material was extracted with three kind of solvent; distilled water, 50% ethyl alcohol, and ether which were immersed in material for 48 hours and concentrated to 10ml by evaporation of solvents. The result was as follow: 1. The anti-inflammatory effect of the sample material on the. edema formed at the rat paw was obviously clear. 2. Many spots of active ingredients were detected on the silica gel G plate spotted by ether extracted material than water one. 3. The good developing solvent was the mixture of $CHCl_3$ ; Acetone : Diethylamine (5:4:1).

• Bulletin of the Korean Chemical Society
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• 제26권3호
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• pp.423-427
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• 2005

The bis(2,4,4-trimethylpentyl)phosphinic acid (Cyanex-272) and sodium diethyl- dithiocarbamate (NaDDC) ligands were used to extract of metal ions ($Cd^{2+},\;Co^{2+},\;Cu^{2+},\;Pb^{2+},\;Zn^{2+}$) in supercritical $CO_2$. Experiments showed a strong synergistic effect and better extraction efficiency if the two ligands were used together. In-situ UV-visible observation indicates that NaDDC in the water/supercritical $CO_2$ started to decompose slowly. The synergistic effect seems to come from the deprotonation of the organophosphorus ligand by amines from the decomposed NaDDC. The enhancing role of amines was confirmed using the mixture of Cyanex-272 and diethylamine(DEA) in the metal extraction.

• 약학회지
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• 제54권6호
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• pp.466-473
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• 2010

A series of $3{\beta}$-substituted 5-androstene-$17{\beta}$-carboxamides were synthesized from analogs of $3{\beta}$-hydroxy-5-androstene-$17{\beta}$-carboxylic acid (1) with tert-butylamine, N,N-diethylamine and 3-aminopyridine and some compounds were epoxidized with mCPBA. A rat prostate testosterone $5{\alpha}$-reductase inhibitory activity of synthesized compounds was assessed by radioimmunoassay using [1,2,6,7-3H]-testosterone as substrate. All synthesized compounds showed lower activity than finasteride and the N-(3-pyridino)-$3{\beta}$-carboxycarbonyloxy-5-androstene-$17{\beta}$-carboxamide (12) showed weak inhibitory activity ($IC_{50}$: $2.4{\times}10^{-7}M$).

• Archives of Pharmacal Research
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• 제26권12호
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• pp.985-989
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• 2003

An efficient synthesis of 5-chloro-3-[4-(3-diethylaminopropoxy)benzoyl]-2-(4-methoxyphenyl)benzofuran (8), a potent $\beta$-amyloid aggregation inhibitor, is described. 5-Chloro-2-(4-methoxyphenyl)benzofuran (3) was obtained by the one-pot synthesis of 4-chlorophenol with $\omega$(methylsulfinyl)-p-methoxyacetophenone (1) under Pummerer reaction conditions, and it was followed by the desulfurization of the resultant 5-chloro-3-methylthio-2-(4-methoxyphenyl)benzofuran (2e). Acylation of benzofuran 3 with 4-(3-bromopropoxy)benzoyl chloride (6) gave the ketone 7, which was converted into compound 8 by the treatment of diethylamine.

• 한국자기학회:학술대회 개요집
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• 한국자기학회 2002년도 동계연구발표회 논문개요집
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• pp.104-105
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• 2002

Ni$_{1-x}$-Zn$_{x}$ ferrite는 매우 큰 저항과 적은 eddy current loss를 가지고 있어 transfomer core나 radio frequency coil같은 high power device등의 전자 재료로 이용된다[1]. Ni$_{1-x}$-Zn$_{x}$ ferrite의 합성에는 여러 가지 방법이 이용되고 있으나 oxide/carbonate를 이용하여 120$0^{\circ}C$ 이상의 고온의 열을 가해 하소하는 solid-state reation과 diethylamine을 이용하여 metal nitrate를 공침 하는 coprecipition방법, sol-gel 방법 등의 wet chemical method가 가장 일반적이다[2-3]. (중략)

• Korean Chemical Engineering Research
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• 제48권1호
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• pp.121-127
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• 2010

본 연구의 목적은 효소법을 이용한 바이오디젤의 생산에서의 효소(lipase) 활성화를 최적화함에 있다. 효과적인 방법으로 효소를 고정하기 위해 방사선 그라프트 중합법을 이용한 부직포에 음이온 교환기인 ethanolamine과 diethylamine을 도입시켜 음이온 교환 부직포(이때 얻어진 부직포는 EtA, DEA-EtA 부직포라 함)를 합성하였다. 기존에 사용하던 다공성 중공사막의 경우 시간이 지남에 따라 막힘 현상에 따라 유속이 현저하게 줄어드는 점을 보완하고자 기공(pore size)이 $300{\mu}m$인 부직포를 선택하였다. 이 부직포에 음이온 교환기가 도입된 EtA, DEA-EtA 부직포의 최적효소 흡착 특성과 효소 활성도에 대하여 고찰하였다. 그 결과 효소 흡착량은 EtA, DEA-EtA 부직포가 비슷하였으나(EtA non-woven fabric: 15.69 mg/g, DEA-EtA non-woven fabric: 14.45 mg/g) 기름을 투과시킨 결과 효소 활성화는 DEA-EtA 부직포가 EtA 부직포에 비해 현저히 떨어짐(EtA non-woven fabric: $3.50mol/h{\cdot}kg$, DEA-EtA non-woven fabric: $0.38mol/h{\cdot}kg$)을 알 수 있었다. 이 음이온교환기를 이용해 효율적인 바이오디젤 생산을 위한 온도, 효소고정량, 기름과 알코올과의 관계 등의 최적의 조건을 도출하였다.

• Archives of Pharmacal Research
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• 제29권9호
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• pp.808-813
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• 2006

Two methods for the chiral purity determination of bevantolol were developed, namely capillary electrophoresis (CE) using carboxymethyl-${\beta}$-cyclodextrin (CM-${\beta}$-CD) as a chiral selector and high-perfomance liquid chromatography (HPLC) using a chiral stationary phase. In the HPLC method, the separation of bevantolol enantiomers was performed on a Chiralpak AD-H column by isocratic elution with n-hexane-ethanol-diethylamine (10:90:0.1, v/v/v) as mobile phase. In the CE method, bevantolol enantiomers were separated on an uncoated fused silica capillary with 50 mM amonium phosphate dibasic adjusted to a pH 6.5 with phosphoric acid containing 15 mM CM-${\beta}$-CD as running buffer. Validation data such as linearity, recovery, detection limit, and precision of the two methods are presented. The detection limits of S-(-)-bevantolol were 0.1% and 0.05% for CE and HPLC method, respectively and R-(+)-bevantolol were 0.15% and 0.05% for CE and HPLC method, respectively. There was generally good agreement between the HPLC and CE results.

• KSBB Journal
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• 제31권3호
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• pp.186-191
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• 2016

A liquid chromatographic method for the enantiomer separation of fluoxetine was performed using covalently bonded and coated type polysaccharide-derived chiral stationary phases (CSPs). The degree of enantioseparation is affected by the used CSPs and mobile phases. The performance of Chiralpak IC was superior to the other CSPs used in this study. Out of various solvent composition and additives, the greatest separation and resolution was observed using Chiralpak IC with mobile phase of 2-propanol in hexane with diethylamine as an additive. Semi-preparative separation of fluoxetine was performed on the analytical Chiralpak IC column to obtain (R)- and (S)-fluoxetine enantiomer with high chemical and optical purity. From the overall study, the developed liquid chromatographic method on polysaccharide-derived CSPs is expected to be very useful for the enantiomer separation of fluoxetine.

• 대한화학회지
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• 제57권2호
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• pp.234-240
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• 2013

The synthesis of title compounds were accomplished by synthetic sequence shown in Scheme 1. Chalcones on cyclocondensation with thiourea in ethanol and potassium hydroxide under reflux yielded the respective dihydropyramidin-2(1H)-thiones. Each of the dihydropyrimidin thiones was, then subjected to the Mannich condensation in alkaline medium using three different secondary amines, viz., dimethylamine, diethylamine and morpholine to obtain a new series of S-Mannich bases. All the synthesised compounds ($C_1-C_{15}$) were evaluated for their antiulcer and antibacterial activities. Compounds $C_4$, $C_5$, $C_6$, $C_{14}$ and $C_{15}$ exhibited relatively more potent antiulcer activity but not comparable to the standard; Omeprazole, while $C_1$, $C_2$, $C_3$ and $C_{13}$ were moderate in activity at 100 mg/kg p.o. All the compounds ($C_1-C_{15}$) showed mild to moderate activity against both Gram-positive (S.aureus, L.delbrueckii) and Gram-negative (P.vulgaris, E.coli) bacteria. Amongst the compounds tested, only $C_6$, $C_9$, $C_{12}$ and $C_{15}$ were found to be potent.

• 센서학회지
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• 제32권2호
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• pp.67-74
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• 2023

A microfluidic paper-based analytical device (µPAD) is proposed for the selective detection of ammonia in water by using the modified Berthelot reagent and a fluidic channel consisting of hollow paper. The modified Berthelot reagents were uniformly dispersed in cyclohexane and then immobilized in a detection zone of the µPAD. The loading position of the reagents and the type of a sample flow channel were optimized to achieve a sensitive ammonia detection within a short analytical time. The NH₃ µPAD exhibits a linear colorimetric response to the concentration of ammonia dissolved in water in the range of 1-100 mg L^-1, and its limit-of-detection is 1.75 mg L^-1. In addition, the colorimetric response was not influenced by the addition of 100 mg L^-1 nitrogen containing compounds (sodium nitrate, sodium nitrite, uric acid, hydroxylamine, butylamine, diethylamine) or inorganic salts (NaCl, Na₂HPO₄), presenting the enough selectivity in the detection of water-dissolved ammonia against possible interferents.