• 멤브레인
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• 제26권3호
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• pp.179-186
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• 2016

당뇨병 환자의 혈당을 측정하기 위해 새로운 형태의 페녹시-메틸아미노 포스파젠 진단막을 제조하였다. 먼저 측정 환경이 혈당 측정에 미치는 영향을 조사하였다. 활성화된 진단막을 가지고 5, 15, 25, 35, $45^{\circ}C$ 그리고 상대습도 20%에서 80%까지 변화시키면서 시간에 따른 680 nm에서의 흡광도 변화량(K/S)를 측정하였다. 높은 측정온도와 습도에서도 K/S와 글루코우즈 농도와의 기울기 값(Dose-Response Slope : DRS)은 크게 영향을 받지 않았다. 두 번째로, 제조된 진단막을 여러 환경에서 보관한 후, 보관 환경이 글루코우즈의 농도 측정에 미치는 영향을 조사하였다. 새로운 포스파젠 진단막을 $50^{\circ}C$에서 8주 보관한 후 측정한 결과, 보관시간과 온도가 크게 영향을 주지 않았다. 또 상대습도 80%에서도 새로운 포스파젠 진단막의 안정성이 확인되었다.

• 대한화학회지
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• 제58권5호
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• pp.450-455
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• 2014

In the present study, a series of novel N-(1H-benzo[d]imidazol-2-yl)methyl-5-[(hetero)aryl-1,3,4-oxadiazol-2-yl]methanamine (4a-4j) were efficiently synthesized. Condensation of hydrazide derivative 3 with various carboxylic acid derivatives yielded N-[(1H-benzo[d]imidazol-2-yl)methy](5-substituted-1,3,4-oxadiazol-2-yl)methanamine (4a-4j) and compound 5-{[(1H-benzo[d]imidazol-2-yl)methylamino]methyl}-1,3,4-oxadiazole-2-thiol (4k) was obtained on treating hydrazide 3 with carbon disulfide. All the newly synthesized analogues were characterized by IR, $^1H$ NMR, $^{13}C$ NMR and mass spectral data.

• 미생물학회지
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• 제27권3호
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• pp.304-309
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• 1989

광합성 세균인 Rhodopseudomonus sphaeroiders의 질소고정 효소 합성 및 암모니아 동화 경로에 중요한 glutamine synthetase(GS), glutamate synthase(GOGAT) 및 glutamatc dehydrogenase(GDH) 활성에 미치는 TriazinerP 제초제인 simazine의 영향을 조사하였다. 배양중에 simazine을 처리할 경우 성장 및 in vivo 질소고정효소의 합성 및 GS의 합성이 크게 저해되었다. 그리고 정상 배지에서 배양한 Rp. sphaeroides의 GOGAT 및 GDH의 활성이 GS의 활성보다 simazinc에 의해 더 큰 저해를 받았다. 이상의 결과는 simazine이 Rp. sphacroides의 광합성 과정을 억제하여, 질소고정효소의 합성을 저해하며 이로인해 GS의 합성이 저해될 가능성이 있음을 시사한다고 하겠다.

• Journal of Plant Biology
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• 제31권3호
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• pp.217-226
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• 1988

Effects of simazine [2-chloro-4,6-bis(methylamino)-s-triazine] on the photochemical reactions of isolaed spinach chloroplasts and crude thylakoids of Anabaena inequalis UTEX B-381 were compared. Simazine inhibited photosynthetic O2 evolution and increased the chlorophyll fluorescence in whole cells of Anabaena. The electron transfer from diphenylcarbazide to 2,6-dichlorophenolindophenol was inhibited by simazine treatment in spinach chloroplasts, but not in crude thylakoids of Anabaena. In spinach chloroplasts, the chlorophyll fluorescence was increased by simazine treatment in the presence of diphenylcarbazide and ferricyanide, but not in the presence of diphenylcarbazide and silicomolybdate. In crude thylakoids of Anabaena, simazine treatment did not increase the chlorophyll fluorescence in the presence of either diphenylcarbazide and silicomolybdate, or diphenylcarbazide and ferricyanide. There results suggest that the inhibitory site of simazine on photosynthetic electron transport chain of anabaena is different from that of spinach chloroplasts. And there may be a possiblity that the inhibition site of simazine in Anabaena lies on the donor side of photosystem II, before the site of electron donation by diphenylcarbazide.

• 대한치과의사협회지
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• 제11권1호
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• pp.45-52
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• 1973

Ketamine HC1(Phencyclidine derivative) is a white, crystalline substance with melting point 259℃. It is soluble in water to a 20% clear, colorless solution. a 10% aqueous solution has a pH 3.5. The chemical structure is 2-(O-chlorophenyl)-2-(methylamino) cyclohexanone hydrochloride. It is a rapid acting, nonhypnotic, nonbarbiturate drug with a wide safety margin. The author used the anesthetic ketamine hydrochloride for oral surgery procedure in 16 patients(2 to 33 years). Anesthesia was achieved with a single intramuscular injection by introduction of manufacture. Result obtained as follows : 1. It was easily administered. 2. Onset time was rapid and duration was short. 3. The mild cardiac stimulation resulted in moderate increase in the blood pressure and pulse. 4. There was no significant respiratory depression. 5. The airway can be maintained without artificial support or endotracheal intubation. 6. All protective reflex maintained, which was important in oral surgery. 7. The best results were achieved in pediatric patients than adults.

• Rapid Communication in Photoscience
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• 제2권3호
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• pp.85-88
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• 2013

Silica nanoparticles were synthesized with various silane coupling agents to make specific pathway of electrons and anti-recombination system when solidifying liquid electrolytes. In this study, we used an appropriate method of synthesis for activated silica nanoparticles and silane coupling agents with 3-(triethoxysilyl)propionitrile, Trimethoxy[3-(methylamino)propyl]silane, Triethoxyoctylsilane, and octadecyltrimethoxy silane. Dye-sensitized solar cells using solidified electrolytes with silica nanoparticles exhibit comparatively excellent efficiency, ranging from 2.3 to 7.0% under similar conditions.

• Elastomers and Composites
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• 제34권4호
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• pp.285-291
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• 1999

Effects of catalysts on network structure, hard segment length and distribution of polyurethane foams in the absence of catalysts were investigated. CFC free all MDI-based poly urethane foams were prepared from poly(ethylene adipate)glycol, 4,4'-diphenylmethane diisocyanate, and water. Amino catalysts used were 1,4-diazabicyclo[2,2,2]octane(DABCO), N, N,N',N'-tetramethyl--hexane-1,6-diamine(MR), bis(2-methylamino ethyl)ether(ET), 1,8-diazabicyclo-[5,4,0]-undecene-7(DBU). Dibutyltindilaurate(DBTL) as control was also used. Hard segment components of polyurethane foams were obtained by a selective degradation of polyester chains with 0.01N KOH-methanol solution. The PUFs with DBU catalyst contained more amount of isocyanurate components than other PUFs. On the other hand, the PUFs with ET, MR, DBTL catalysts contained more amount of allophanate and biuret component than the other PUFs.

• Bulletin of the Korean Chemical Society
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• 제19권11호
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• pp.1165-1168
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• 1998

2-Tetrahydropyranyl methacrylate with a self-crosslinkable moiety was copolymerized with methyl methacrylate and 4-[(2-methacryloxyethyl)methylamino]-4'-nitrostilbene or 4-[(2-methacryloxyethyl)ethylamino]-4'nitroazobenzene to provide second-order nonlinear optical property. Glass transition temperatures (Tg of the copolymers are around 140 ℃. The copolymers were soluble in common organic solvents such as tetrahydrofuran (THF), cyclohexanone, and N,N-dimethylformamide (DMF). Poling was carried out at 140 ℃ for 20 min and identified with UV-Vis spectroscopy. Electro-optic coefficient (r33) of copolymer was 62 pm/V for polymer 2 at 633 nm, and relaxation did not remarkably occur due to the formation of a crosslinked network at 200 ℃ for 15 min.

• Archives of Pharmacal Research
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• 제24권6호
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• pp.503-507
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• 2001

trans-Metanicotine, a subtype (${\alpha}_4{\beta}_2$)-selective ligand for neuronal nicotinic acetylcholine receptor, is under clinical phase for Alzheimer's disease. An efficient synthetic route for ($\pm$)-methyl-(1-aryl-4-pyridin-3-yl-but-3-enyl)-am ices, derivatives of tracts-metanicotine, was explored. Allylation reaction of aryl aldimines with allylmagnesium bromide in THF gave ($\pm$)-methyl-(1-aryl-but-3-enyl)-amines. Protection of the amines with the Boc group and following Heck reaction of the N-Boc amines with 3-bromopyridine gave ($\pm$)-methyl-(1-aryl-4-pyridin-3-yl-but-3-enyl)-carbamic acid tert-butyl esters. Deprotection of the N-Boc group in aqueous 1 N-HCI solution gave the titled amines in good yields. Thus, trans-metanicotine analogues modified at the ${\alpha}-position$ of the methylamino group with amyl groups were obtained in 5 steps.

• Archives of Pharmacal Research
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• 제23권3호
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• pp.202-205
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• 2000

A convenient pathway for synthesis of trans-metanicotine analogues was developed. trans-Metanicotine, a subtype(${\alpha}4{\beta}2$)-selective ligand for neuronal nicotinic acetylcholine receptor, is under clinical phase for Alzheimer's disease. Zn-mediated allylation of allyl bromide and acetaldehyde followed by Heck reaction with 3-bromopyridine gave 5-pyridin-3-yl-pent-4-en-3-ol (2). Tosylation of 5-pyridin-3-yl-pent-4-en-3-ol followed by substitution reaction with methylamine in sealed tube gave methyl-(1-methyl-4-pyridin-3-yl-but-3-enyl)-amine (4) in good yields. Thus, trans-metanicotine analogues modified at the $\alpha$-position of the methylamino group with various functional groups can be obtained in 4 steps.