• 대한화학회지
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• 제9권1호
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• pp.61-65
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• 1965

有機클로로酸, 또는 에스타와 各種金屬(亞鉛, 硅素, 마그네슘, 錫)과의 여러 溶媒存在下(아세트나이트라일, 디옥센 및 토루엔)의 反應에서 얻은 反應生成物, 또는 反應系中의 金屬分布狀態를 (n,${\gamma}$)反應으로 製造한 各種放射性 金屬트레이서를 使用하여 決定하였다. 有機클로로 金屬 콤푸렉스의 溶解度는 親水性溶媒에서는 顯著하게 增加하였으며, 無極性溶媒에는 減少하였다. 이 事實은 回收된 金屬, 또는 回收된 金屬混合物의 水洗液中의 金屬分布狀態의 增加로서 確認되었다. 카보닐化合物 存在下에서 反應시켰 때에도 같은 事實을 나타내었다. 親水性溶媒中의 金屬콤푸렉스의 溶解度는 亞鉛, 硅素, 錫 및 마그네슘이 順序로 減少되었으며 無極性溶媒下에서는 硅素, 錫, 마그네슘 및 亞鉛의 順으로 減少되었다. 有機할로겐化合物과 金屬과의 反應生成物로 普通 豫期되는 有機金屬化合物은 全反應을 通하여 거의 없었다. 反應結果를 論議하였으며, 本反應過程에서 觀察한 溶媒의 影響에 關하여 論及하였다.

• Asian Pacific Journal of Cancer Prevention
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• 제16권14호
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• pp.5883-5887
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• 2015

Despite recent advances in therapeutic strategies for lung cancer, mortality still is increasing. In the present study, we investigated the anti-cancer effects of KMU-193, 2-(4-Ethoxy-phenyl)-N-{5-[2-fluoro-4-(4-methylpiperazine-1-carbonyl)-phenylamino]-1H-indazol-3-yl}-acetamide in a human non-small cell lung cancer cell line A549. KMU-193 strongly inhibited the proliferation of A549 cells, but it did not have anti-proliferative effect in other types of cancer cell lines. KMU-193 further induced apoptosis in association with activation of caspase-3 and cleavage of PLC-${\gamma}1$. However, KMU-193 had no apoptotic effect in untransformed cells such as TMCK-1 and BEAS-2B. Interestingly, pretreatment with z-VAD-fmk, a pan-caspase inhibitor, strongly abrogated KMU-193-induced apoptosis. KMU-193 treatment enhanced the expression levels of p53 and PUMA. Importantly, p53 siRNA transfection attenuated KMU-193-induced apoptosis. Collectively, these results for the first time demonstrate that KMU-193 has strong apoptotic effects on A549 cells and these are largely mediated through caspase-3- and p53-dependent pathways.

• Bulletin of the Korean Chemical Society
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• 제31권4호
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• pp.934-940
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• 2010

The reduction of [$Os_3(CO)_{11}P(OMe)_3$] and subsequent ionic coupling of the reduced species with $[Ru({\eta}^5-C_5H_5)(CH_3CN)_3]^+$ resulted in the formation of [$Os_3(CO)_{11}P(OMe)_3(Ru({\eta}^5-C_5H_5))_2$] which can be converted to spiked tetrahedral cluster, [$HOs_3(CO)_{11}P(OMe)_3Ru_2({\eta}^5-C_5H_5)(C_5H_4)$] via the intramolecular hydrogen transfer. Due to the unavailability of a suitable single crystal, the PW91/SDD and LDA/SDD density functional methods were used to predict possible structures and the available spectroscopic information (IR, NMR) of [$Os_3(CO)_{11}P(OMe)_3(Ru({\eta}^5-C_5H_5))_2$]. The most probable geometry found by constrained search is the isomer (a2) in which the phosphite, $P(OMe)_3$, occupies an axial position on one of the two osmium atoms that is edge bridged by the $Ru(CO)_2({\eta}^5-C_5H_5)$ unit. By using the most probably geometry, the predicted infrared frequencies and $^1H$, $^{13}C$ and $^{31}P$ NMR chemical shifts of the compound are in the same range as the experimental values. For this type of complex, the LDA/SDD method is appropriate for IR predictions whereas the OPBE/IGLO-II method is appropriate for NMR predictions. The activation energy and reaction energy of the intramolecular hydrogen transfer coupled with the structural change of the transition metal framework were estimated at the PW91/SDD level to be 110.32 and -0.14 kcal/mol respectively.

• Bulletin of the Korean Chemical Society
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• 제28권11호
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• pp.1958-1962
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• 2007

The title complex, Ir(H)(CO)(PEt3)2(η 2-C60) (2), has been prepared by the reaction of excess C60 (4 equiv) with a tetrairidium complex Ir4(CO)8(PEt3)4 (1) in refluxing chlorobenzene in 40% yield as green crystals. Compound 2 has been characterized by cyclic voltammetry (CV), spectroscopic methods (mass, IR, 1H and 31P NMR), and a single crystal X-ray diffraction study. The molecular structure reveals that the iridium atom of 2 is coordinated by two axial ligands of a hydrogen atom and a carbonyl group, and three equatorial ligands of two phosphorus atoms and an η 2-C60 moiety. The CV study exhibits three reversible one-electron redox waves for the successive reductions of 2, together with additional four redox waves due to free C60 reductions, which was formed by decomposition of 2 in the reduced states. The three reversible redox waves of 2 are shifted to more negative potentials by ca. 270 mV compared to free C60, reflecting both metal-to-C60 π-back-donation and the electron-donating nature of the two phosphorus ligands.

• 한국연초학회지
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• 제29권1호
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• pp.30-40
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• 2007

The objective of this study was to investigate the contribution of various smoke constituents to the toxicological activity of total particulate matter(TPM) or the gas/vapor phase(GVP). These components included phenol compounds, aromatic amines, polycyclic aromatic hydrocarbons, heterocyclic amines, and carbonyl compounds. The mutagenic and cytotoxic potencies were assessed using the Salmonella mutagenicity assay with S. typimurium TA98 strain and the neutral red uptake cytotoxicity assay(NRU) with BALB/c 3T3 fibroblast cells, respectively. The Salmonella mutagenicity test showed that heterocyclic amines exhibited significantly higher levels of toxicity compared to other smoke constituents. Among them, 2-amino-3,4-dimethylimidazo[4,5-f]quinoline(MeIQ) was shown the most mutagenic compound with a specific mutagenicity of $7.9{\times}10^5\;revertants/{\mu}g$. An analysis of the possible contribution revealed that MeIQ account for only 0.85% of the 2R4F-TPM mutagenicity in TA98. NRU data demonstrated that high cytotoxic activity was obtained for hydroquinone, formaldehyde, and acrolein. Based on the results of the present study, the contribution of acrolein to the cytotoxicity of the GVP fraction was calculated as 61%. Thus, a large proportion of the cytotoxic activity of this complex mixture, cigarette smoke gas phase, can be attributed to the acrolein.

• 한국식품과학회지
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• 제34권6호
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• pp.984-991
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• 2002

순수 참기름과 채종유, 옥수수유, 대두유를 10%, 30%, 50%씩 첨가한 참기름 혼합유를 제조하여 $60^{\circ}C$의 incubator에서 8주간 저장하면서 혼합유의 산화 안정성과 향기 성분의 변화 그리고 관능 검사를 실시하였다. 모든 시료의 POV는 저장 6주에 최고값을 나타내었으며 채종유와 옥수수유 10%, 30%, 50%씩 그리고 대두유 10%를 첨가한 참기름 혼합유는 순수 참기름 보다 저장 기간 동안 과산화물 생성이 억제되어지는 효과가 있음을 나타났다. 산패 유도기간도 채종유와 옥수수유 10%, 30%, 50%씩 그리도 대두유 10%를 첨가한 참기름 혼합유에서는 대조구인 참기름 보다 그 기간이 더 연장되었다. 상대적 항산화 효과(Relative Antioxidant Effectiveness: RAE)는 10% 채종유를 첨가한 혼합유가 순수한 참기름 보다 6배의 효과가 있었다. 그리고 산가는 모든 혼합유 시료가 참기름 보다 더 낮은 결과를 나타내었으나 단일 식물성유 보다는 그 수치가 높았다. 혼합유의 향기 성분은 참기름에서 확인된 참기름의 독특한 방향을 나타내는 pyrazine류가 참기름 혼합유에서도 확인되었으며 저장 기간이 연장됨에 따라 모든 시료에서 산패의 지표가 되는 aldehyde, ketone, acid등의 carbonyl 화합물의 함량이 증가되었다. 관능평가에서는 10%의 채종유, 옥수수유, 대두유를 첨가한 참기름 혼합유 시료는 대조구인 순수 참기름과 유의적인 차이가 없는 것으로 밝혀졌다. 이와 같은 결과로 미루어 볼 때 참기름과 식물성유의 혼합은 매우 바람직하며 단일 식물성유보다 산화 안정성이 크게 증대되었을 뿐 아니라 관능적인 품질에도 차이가 없으므로 경제적인 면에서도 매우 유용할 것으로 생각된다.

• Bulletin of the Korean Chemical Society
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• 제16권2호
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• pp.112-120
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• 1995

The conformational study on malonic acid, hydrogen malonate, malonate, malonyl methyl sulfide, and malonyl methyl sulfide anion, as the model compounds of malonyl-CoA, was carried out using the semiempirical MO methods (MNDO, AM1, and PM3) and hydration shell model. On the whole, the feasible conformations of malonic acid, hydrogen malonate, and malonate seem to be similar to each other. In malonic acid and malonate, two carboxyl groups are nearly perpendicular to the plane of the carbon skeleton, despite of different orientation of two carboxyl groups themselves. In particular, two carboxyl groups of hydrogen malonate are on the plane formed by carbon atoms with an intramolecular hydrogen bond. The calculated results on the geometry and conformation of three compounds are reasonably consistent with those of X-ray and spectroscopic experiments as well as the previous calculations. The orientation of two carbonyl groups of malonyl methyl sulfide is quite similar to that of malonic acid, but different from that of its anion. Especially, the computed probable conformations of the sulfide anion by the three methods are different from each other. The role of hydration seems not to be crucial in stabilizing the overall conformations of malonic acid, hydrogen malonate, malonate, and malonyl methyl sulfide. However, the probable conformations of the unhydrated sulfide anion obtained by the MNDO and AM1 methods become less stabilized by including hydration. The AM1 method seems to be appropriate for conformational study of malonyl-CoA and its model compounds because it does not result in the formation of too strong hydrogen bonds and significant change in conformational energy from one compound to another.

• 한국환경보건학회지
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• 제45권5호
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• pp.474-486
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• 2019

Objectives: This study was performed to investigate the emission characteristics of aldehydes emitted by the printing industry and to evaluate their impact on adjacent residential areas. Methods: Aldehydes and THC were measured from the front of the control device in the printing and coating process. Aldehydes and ketones were measured by workplace area, residential area, and background area to evaluate their impact. Results: The concentrations of formaldehyde (<0.047 ppm) and acetaldehyde (<0.068 ppm) in the printing and coating process were relatively low, and the methyl ethyl ketone used as the primary solvent was the main carbonyl compound in the printing process. The daily mean concentrations of formaldehyde and acetaldehyde were not significantly different by workplace area, residential area, or background area. However, the concentration of methyl ethyl ketone was high in the order of workplace area, residential area, and background area. Conclusions: The concentrations of formaldehyde and acetaldehyde in the adjacent residential areas are considered to be more influenced by secondary sources of photochemical reactions than by primary sources. Methyl ethyl ketone is considered to be highly influenced by the primary source, which is printing facilities.

• Safety and Health at Work
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• 제10권2호
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• pp.229-236
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• 2019

Background: Emerging reports suggest the potential for adverse health effects from exposure to emissions from some additive manufacturing (AM) processes. There is a paucity of real-world data on emissions from AM machines in industrial workplaces and personal exposures among AM operators. Methods: Airborne particle and organic chemical emissions and personal exposures were characterized using real-time and time-integrated sampling techniques in four manufacturing facilities using industrial-scale material extrusion and material jetting AM processes. Results: Using a condensation nuclei counter, number-based particle emission rates (ERs) (number/min) from material extrusion AM machines ranged from $4.1{\times}10^{10}$ (Ultem filament) to $2.2{\times}10^{11}$ [acrylonitrile butadiene styrene and polycarbonate filaments). For these same machines, total volatile organic compound ERs (${\mu}g/min$) ranged from $1.9{\times}10^4$ (acrylonitrile butadiene styrene and polycarbonate) to $9.4{\times}10^4$ (Ultem). For the material jetting machines, the number-based particle ER was higher when the lid was open ($2.3{\times}10^{10}number/min$) than when the lid was closed ($1.5-5.5{\times}10^9number/min$); total volatile organic compound ERs were similar regardless of the lid position. Low levels of acetone, benzene, toluene, and m,p-xylene were common to both AM processes. Carbonyl compounds were detected; however, none were specifically attributed to the AM processes. Personal exposures to metals (aluminum and iron) and eight volatile organic compounds were all below National Institute for Occupational Safety and Health (NIOSH)-recommended exposure levels. Conclusion: Industrial-scale AM machines using thermoplastics and resins released particles and organic vapors into workplace air. More research is needed to understand factors influencing real-world industrial-scale AM process emissions and exposures.

• 한국수산과학회지
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• 제31권4호
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• pp.594-598
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• 1998

패류 건제품의 지질산화는 주로 단백질과의 상호반응에 의해 변색, 산패취 등을 일으키며 또한 산화로 인해 hydroperoxide나 불포화 aldehyde 등과 같은 독성물질을 생성한다고 알려져 있다. 특히 건제품의 저장 중에 발생하는 지질과 단백질의 반응에 의한 품질저하는 상품가치의 저하는 물론 영양가 손실 등을 야기한다. 본 실험에서는 이들 패류 건제품의 저장온도 ($4{\pm}2^{\circ}C$ 및 $25{\pm}2^{\circ}C$)에 따른 지질산화 경향을 지질산화생성물과 단백질 등의 amino 화합물과의 반응정도를 조사하였다. 산가의 변화는 홍합이나 바지락 모두 $25^{\circ}C$에서 저장한 것이 $4^{\circ}C$에서 저장한 것보다 높았으며 또한 저장온도에 관계없이 바지락이 홍합보다 다소 높았다. 그러나 생성된 유리지방산은 저장 60일까지 증가한 후 거의 변화가 없었다. 과산화물가는 $25^{\circ}C$ 저장구의 경우 홍합 및 바지락이 각각 저장 60일과 30일까지 증가한 후 감소하였으나, $4^{\circ}C$ 저장구에서는 120일간의 저장기간 중 과산화물이 분해되지 않고 지속적으로 축적되었다. TBA가와 카르보닐가는 홍합의 경우 $4^{\circ}C$ 저장구가 저장 30일경에만 $25^{\circ}C$ 저장구보다 낮은 값을 나타내었을 뿐 그 이후는$25^{\circ}C$ 저장구보다 높은 값을 나타내며 증가하는 경향이었다. 또한 바지락도 $4^{\circ}C$ 저장구가 $25^{\circ}C$ 저장구보다 다소 높은 값을 유지하였다. 아미노질소의 함량은 두 제품모두 저장 60일까지 증가한 후 감소하였으며, $25^{\circ}C$ 저장시료가 $4^{\circ}C$ 저장시료보다 감소폭이 컸다. 형광강도는 $25^{\circ}C$ 저장시료가 $4^{\circ}C$ 저장시료보다 그리고 바지락이 홍합보다 높았으며, 저장 60일 이후 감소하는 경향을 나타내었다.