• 한국수산과학회지
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• 제34권5호
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• pp.509-514
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• 2001

기능성물질인 CLA를 양어사료에 첨가하여 기존의 어류와는 다른 기능성 역돔 생산을 시도하였다. 사육 8주간 매 2주마다 어체내의 CLA축적도를 측정한 결과 8주 후 $1\%$ CLA 첨가구에서는 41.3 mg/g of fat였으며, $10\%$ CLA 첨가구에서는 180.9mg/g of fat으로 역돔의 정상적인 성장을 고려하지 않는다면 $10\%$의 사료내 첨가도 가능한 것으로 생각된다. 그러나 정상적인 성장을 고려하면 CLA의 적정 첨가량은 $1\%$로 나타났으며, 그 이상의 첨가시에는 성장 저하 현상을 나타내었다. 합성된 CLA는 총 6 종류의 이성체로 구성되어 있었고, 그 중 c9, t11 및 t10, c12 이성체가 $85\sim90\%$를 이루고 있었으며, 첨가된 CLA 함량에 따라 축적되는 양도 달라졌다. 사육 8주 후, 육 및 간 중의 지방산 조성은 n-9, 3 계열은 거의 화를 나타내지 않았으나, n-6계열은 첨가된 CLA의 함량에 따라 육 및 간에 축적되는 양은 $5\sim27\%$로, $1\%$ CLA 첨가구가 가장 높았고, $10\%$ CLA 첨가구가 가장 낮은 함량비를 나타내었다.

• Journal of Information Display
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• 제12권3호
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• pp.145-152
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• 2011

Since the discovery of fullerenes as a class of nanostructure compounds, many potential applications have been suggested for their unusual structures and properties. The isolated pentagon rule (IPR) states that all pentagonal carbon rings are isolated in the most stable fullerene. Fullerenes $C_n$ are a class of spherical carbon allotrope group with unique properties. Electron transfer between fullerenes and other molecules is thought to involve the transfer of electrons between the molecules surrounding the fullerene cage. One class of electron transfer molecules is the methanofullerene derivatives ([6,6]-phenyl $C_{61}$-butyric acid methyl ester (PCBM), 4-(2-ethylhexyloxy)-[6,6]-phenyl $C_{61}$-butyric acid methyl ester (p-EHO-PCBM), and 4-(2-ethylhexyloxy)-[6,6]-phenyl $C_{61}$-butyric acid (p-EHO-PCBA), 10-12). It has been determined that $C_{60}$ does not obey IPR. Supramolecular complexes 1-9 and 10-12 are shown to possess a previously unreported host.guest interaction for electron transfer processes. The unsaturated, cis-geometry, thiocrown ethers, (1-9) (described as [X-UT-Y], where X and Y indicate the numbers of carbon and sulfur atoms, respectively), are a group of crown ethers that display interesting physiochemical properties in the light of their conformational restriction compared with a corresponding saturated system, as well as the sizes of their cavities. Topological indices have been successfully used to construct mathematical methods that relate structural data to various chemical and physical properties. To establish a good relationship between the structures of 1-9 with 10-12, a new index is introduced, ${\mu}_{cs}$. This index is the ratio of the sum of the number of carbon atoms ($n_c$) and the number of sulfur atoms ($n_s$) to the product of these two numbers for 1-9. In this study, the relationships between this index and oxidation potential ($^{ox}E_1$) of 1-9, as well as the first to third free energies of electron transfer (${\Delta}G_{et(n)}$, for n = 1-3, which is given by the Rehm-Weller equation) between 1-9 and PCBM, p-EHO-PCBM, and p-EHO-PCBA (10-12) as [X-UT-Y]@R(where R is the adduct PCBM, p-EHO-PCBM, and p-EHO-PCBA group) (13-15) supramolecular complexes are presented and investigated.

• 생명과학회지
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• 제16권3호
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• pp.546-554
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• 2006

식용 및 약용으로 이용되는 산초 (Zanthoxylum schinifolium) 잎에 함유된 항암활성 성분을 분리하기 위하여 산초잎을 유기용매로 추출하여, 각 추출물의 암세포에 대한 독성 및 세포자살 유도 활성을 조사하였다. Methanol, methylene chloride, ethyl acetate, n-butanol로 추출한 각 추출물의 세포 독성을 인체 급성백혈병 Jurkat T 세포주, estrogen receptor-positive 유방암 세포주 MDA 361과 estrogen receptor-negative 세포주 MDA 438를 대상으로 조사한 결과, 이들 암세포주에 대한 세포독성이 methylene chloride 추출물 (SL-14)에서 주로 확인되었다. Methylene chloride 추출물 (SL-14)의 Jurkat T세포주에 대한 세포독성의 기전은 mitochondria로부터cytochrome c 방출, 이에 뒤이은 caspase-9 및 caspase-3의 활성화, PARP 분해, jnternucleosomal DNAfragmentation등의 일련의 생화학적 과정을 통해 유도되며 또한 Bcl-xL의 ectopic overexpression에 의해서는 negative regulation되는 세포자살임을 확인하였다. 또한 SL-14를 GC-MS 분석하여, 9,19-cyclolanost-24-en-3-ol (15.1%), 2-a-methyl-17, b-hop-21-ene (15.1%), 15-methyl-2,3-dihydro-1H benzazepin (11.95%), phytol (10.38%), lupeol (9.92%), 12-methylbenzofuran (8.23%) 등을 포함한 22가지의 구성성분과 그 조성비를 확인하였다. 이상의 연구결과들은 식용 산초잎에 함유된 항암 활성으로서의 세포자살유도 활성의 규명과 이해에 유익하게 활용될 것으로 기대된다.

• Bulletin of the Korean Chemical Society
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• 제33권9호
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• pp.3017-3024
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• 2012

The geometrical parameters, vibrational frequencies, and binding energies for $(H_2O_3)_n$ (n = 1-5) have been investigated using various quantum mechanical techniques. The possible structures of the clusters (n = 2-5) are fully optimized and the binding energies are predicted using energy differences at each optimized geometry. The harmonic vibrational frequencies are also determined and zero-point vibrational energies (ZPVEs) are considered for the better prediction of the binding energy. The best estimation of the binding energy for the dimer is 8.65 kcal/mol. For n = 2 and 3, linear structures with all trans forms of the HOOOH monomers are predicted to be the lowest conformations in energy, while the cyclic structures with all cis-HOOOH monomers are preferable structures for n = 4 and 5.

• Bulletin of the Korean Chemical Society
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• 제35권9호
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• pp.2738-2742
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• 2014

Geometry relaxation effects on the formation of benzene excimer were investigated by means of ab initio calculation at SOS-CIS($D_0$)/aug-cc-pVDZ level. In the case of T-shaped dimer configuration, intermolecular interactions in the excited states are found to be nearly the same as those in the ground state and structural deformations are limited within a single molecule; the geometry relaxation effects are then negligible and singlet-triplet energy gap remains constant. As for face-to-face eclipsed dimer, on the other hand, both molecules undergo structural change. As a result, intermolecular interactions in the excited states are significantly different than those in the ground state. Although the intermolecular distances obtained from potential energy curve calculation with frozen molecular structures are in qualitative agreement, the excited-state binding energies are notably overestimated with respect to those at optimized structures. In particular, the effects are calculated to be larger in $T_1$ state and hence singlet-triplet energy gap, which reduces markedly in this configuration, is underestimated without relaxation.

• Asian Pacific Journal of Cancer Prevention
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• 제13권9호
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• pp.4677-4681
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• 2012

Objective: Egg consumption has been suggested to increase the risk of colorectal and some other cancers. The present study summarized and quantified the current evidence relating dietary intake of eggs and prostate cancer. Materials and methods: Literature searches were conducted to identify peer-reviewed manuscripts published up to July 2012. Twenty manuscripts from nine cohort studies and 11 case-control studies were identified. Summary risk estimates with 95% confidence intervals (CIs) were calculated for case-control and cohort studies separately. Results: Neither the case-control not the cohort studies showed any association of prostate cancer incidence with egg consumption (case-control studies: odds ratio 1.09, 95% CI 0.86-1.31; cohort studies: relative risk 0.97, 95% CI 0.97-1.07). The results were consistent in subgroup analysis. Furthermore, no association was observed between egg consumption and prostate cancer-specific mortality. Conclusions: Our analyses provided no evidence of a significant influence of egg consumption on prostate cancer incidence and mortality. However, more studies, particularly large prospective studies, are needed.

• Journal of Power Electronics
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• 제9권2호
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• pp.198-206
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• 2009

An algorithm is developed that enables a single-phase matrix converter (SPMC) to perform functions of a generalized single phase power electronics converter such as acting as a frequency changer, rectifier, inverter, and chopper. This reduces the need for new converter hardware. The algorithm is implemented first on computer simulation software Orcad Capture CIS version 9.1. Simulation results are presented for five types of converters with a control input variable that decides the 1) type of converter and 2) type of output waveform. The simulated results verify the working and operation of a generalized converter based on SPMC. Simulated results are verified with experimental results. Hardware design is obtained using readily available ICs and other components. The trigger circuit has been tested qualitatively by observing waveforms on CRO. The operation of the proposed system has been found to be satisfactory.

• Bulletin of the Korean Chemical Society
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• 제19권1호
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• pp.86-93
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• 1998

Trans-4-(9-anthrylethenyl)-4'-methyl-2,2'-bipyridine(t-aemb) and its bipyridyl Ru complex $[Ru(bpy)_2(t-aemb)](PF_6)_2$ (bpy=2,2'-bipyridine) 1 have been prepared and their excited state properties have been studied. t-Aemb exhibits solvent-dependent fluorescence and efficient trans→cis photoisomerization. 1 shows very weak fluorescence and its photochemically reactive. Fluorescence is wavelength-dependent. While the excitation into the MLCT band makes the complex fluorescent, direct absorption by the t-aemb ligand leads to the photoreaction of t-aemb ligand and no fluorescence is observed. 1 is considered to behave in part as bichromophoric molecule in which $[Ru(bpy)_3](PF_6)_2$ and anthryl group are covalently linked by ethenyl linkage. Because anthryl moiety is not effectively conjugated with bipyridylethenyl moiety due to steric hindrance, weak fluorescence can be explained due to the efficient energy or electron transfer.

• Bulletin of the Korean Chemical Society
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• 제9권3호
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• pp.144-149
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• 1988

Reaction of thianthrene cation radical perchlorate (1) with 1-methyl-4-benzenesulfonylaminobenzene (10) afforded thianthrene (5), N-(4-tolyl)-N-thianthrenylbenzenesulfonamide (14), 1-methyl-3-[N-(4-tolyl)-N-benzenesulfonyl-amino- 4-benzene-sulfonylaminobenzene (16), cis-thianthrene-5,10-dioxide (17), 5-(3'-methyl-6-benzenesulfonylaminobenzene)thian threnium perchlorate (18), and benzenesulfonate. In the meantime, reaction of 1 with 1-ethyl-4-benzenesulfonylaminobenzene (12) afforded 5, 1-ethyl-3-[N-(4-ethylphenyl)-N-benzenesulfonyl]a mino-4-benzenesulfonylaminobenzene (19), 1-benzenesulfonyl-amino-4-[1-(2-benzenesulfonyla mino-5-ethylphenyl)ethyl]benzene (20), and 1-(1-acetamidoethyl)-4-benzenesulfonylaminobenz ene (21). The formations of these products except for 18 and benzenesulfonate could be rationalized by assuming a sulfonamidyl radical as an intermediate.

• Bulletin of the Korean Chemical Society
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• 제15권9호
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• pp.766-771
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• 1994

A number of molybdenum(VI), -(V), and -(IV) oxo complexes with S-methyl 3-(2-hydroxyphenyl)methylenedithiocarbazate and its derivatives as the ONS-donor metal-binding substrate are synthesized. The Mo(VI)-dioxo complexes are cis-dioxo Mo$O_2$L(D), where D is solvent molecules such as MeOH, DMF, Py(pyridine), DMSO, and ${\gamma}$-Pic(${\gamma}$-picoline). The Mo(V)-oxo complexes are of the type (PyH)[MoO(NCS$)_2$L] with an octahedral geometry. The Mo(IV)-oxo complexes, MoOL are derived from corresponding Mo(VI)-dioxo complexes by oxo abstraction with PP$h_3$. The complexes are characterized by IR, $^1$H-NMR, UV-Vis spectroscopy and cyclic voltammetry. On the basis of ligand displacement reaction, the qualitative order of D binding for Mo$O_2$L(D) complexes is also discussed.