• Bulletin of the Korean Chemical Society
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• 제9권3호
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• pp.167-171
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• 1988

Formation of intermolecular charge-transfer complexes between 7,7,8,8-tetracyanoquinodimethane (TCNQ) and two different series of stilbene derivatives has been studied spectroscopically at $25^{\circ}$C in 1,2-dichloroethane. The compounds of Series I include stilbene and derivatives which have fused phenyl rings on one end of the central ethylene structure and a phenyl ring on the other end. The other Series, II, is comprised of stilbenes which have various para substituents on one of the two phenyl rings. The equilibrium constant, $K_c^{AD}$ and the molar extinction coefficient, ${\varepsilon}_{\lambda}^{AD}$, were determined using the Scott equation. The values of the charge-transfer transition frequency, ${\vu}_AD$ and $K_c{AD}$ correlated well respectively with the ionization potentials of the fused rings of Series Ⅰ or of the compounds of Series II and with the values of ${\sigma}_p$, the Hammett constants of the Series II substituents. trans-4-N,N-Dimethylaminostilbene and trans-4-nitrostilbene were found to be able to participate in electron transfer reaction with TCNQ forming the corresponding anion radical, TCNQ$^-$:

• Applied Biological Chemistry
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• 제50권3호
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• pp.178-186
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• 2007

항균균활성이 있는 4-isopropylphenol(I)과 2-isopropylphenol (II)을 출발물질로 하여 ester, sulfonyl ester, phosphoyl ester와 ether계열 유도체 42종을 합성하였으며, 확인은 IR, $^{1}H-NMR$과 GC/MS를 이용하였다. 이들 유도체들에 대한 in vitro 항균활성 실험을 오이탄저병균(Colletotrichum orbiculare) 외 9종에 대하여 실시하였다. 그 결과, 2-isopropylphenyl piperonyloate(II-7a)가 오이탄저병균(Colletotrichum orbiculare)과 토마토잎마름병균(Phytophthora infestans)에 효과가 있었으며, 4-isopropylphenyl bromoacetate(I-3a)가 오이잿빛곰팡이병균(Botrytis cinerea), 4-isopropylphenyl-4-methoxybenzenesulfonate(I-6b)는 벼도열병균(Pycularia oryzae)에 탁월한 효과를 나타내었으며, 4-isopropylphenylbenzyl ether(I-4d)가 오이탄저병균(Colletotrichum orbiculare)에 우수한 효과를 나타내었다. In vivo 실험에서는 2-isopropylphenyl piperonyloate(II-7a)가 오이탄저병(Colletotrichum orbiculare)과 토마토잎마름병(Phytophthora infestans), 4-isopropylphenyl 4-methoxybenzenesulfonate(I-6b)가 벼도열병(Pycularia oryzae)에 매우 우수한 항균활성을 나타내었다.

• Journal of Periodontal and Implant Science
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• 제38권4호
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• pp.679-690
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• 2008

Purpose: The aim of this study was to investigate the effects of EMD on demineralized root surface using human periodontal ligament cells and compare the effects of root conditioning materials(tetracycline(TCN), EDTA). Material and Methods: Dentin slices were prepared from the extracted teeth and demineralized with TCN and EDTA. Demineralized dentin slices were incubated at culture plate with 25, 50 and $100{\mu}g/ml$ concentration of EMD. Cell attachment, alkaline phosphatase activity test, protein synthesis assay and scanning electronic microscopic examination were done. Results: Cells were attached significantly higher in EMD treated group at 7 and 14 days. Cell numbers were significantly higher in EMD treated group. Alkaline phosphatase activity was significantly higher in EMD treated group at 7 and 14 days. Protein synthesis was significantly higher in EMD treated group at 7 and 14 days. Conclusion: Enamel matrix derivatives enhance the biologic activities of human periodontal ligament cells on demineralized root surface and its effects are dependent on the concentration of EMD.

• 한국식품과학회지
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• 제22권5호
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• pp.543-548
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• 1990

살구의 휘발성 향기성분 조성에 대한 분리 방법의 영향을 조사코저 살구 과육(pH 3.1)을 simultaneous distillation-extraction(SDE)법, headspace trapping법 또는 이를 pH 7.0으로 중화시킨 후 SDE법에 의해 얻어진 정유성분의 조성을 분석 비교하였다. GC-MS 및 GC에 의한 표준품과 머무름 시간의 비교에 의해 확인된 80종의 성분들 중 pH3.1에서 SDE법에 의해 얻어진 정유성분중에는 다른 두 가지 방법에 의해 얻어진 정유성분에서는 검출되지 않거나 또는 미량으로 검출된 n-hexanal, trans-2-hexenal, cis-3-hexen-1-ol, linalool oxide, linalool, ${\alpha}-terpineol$, nerol, geraniol, benzyl alcohol, ${\beta}-phenylethyl alcohol$ 및 naphthalene 유도체들이 많이 검출되었으며 이러한 결과는 살구에서 비휘발성인 glycoside 형태로 존재하는 위와 같은 성분들이 산성조건하에서 수증기 증류시 glycoside 결합이 가수분해되어 휘발성 성분으로 유리되는데 기인하는 것으로 판단되었다.

• 대한화학회지
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• 제58권4호
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• pp.381-387
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• 2014

A series of new $N^7$-tetrazolo[5,1-f ]-1,2,4-triazin-8-(7H)-one derivatives 4-16 were designed and synthesized from 3 with different reagents. The newly prepared compounds were characterized by spectral data and screened for their antimicrobial activities against various bacteria and fungi strains.

• Bulletin of the Korean Chemical Society
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• 제32권7호
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• pp.2428-2432
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• 2011

A series of new 4-aryl-6,8-dimethylpyrimido[4,5-c]pyridazine-5,7(6H,8H)-diones have been synthesized via three component reaction of 1,3-dimethylbarbituric acid with arylglyoxals in the presence of hydrazinium dihydrochloride in ethanol. All of these derivatives may act as potential monoamine oxidase inhibitors.

• Bulletin of the Korean Chemical Society
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• 제17권5호
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• pp.437-442
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• 1996

Electrocyclic ring-closure of 6-vinylcyclohepta-1,3,5-isocyanate has been carried out in the presence of triphenylphosphine to examine a catalyzing effect of the triphenylphosphine. The preparation of 10-(1-carboalkoxyalkyl)-2,7-methanoaza[10]annulenes by the electrocyclic ring-closure of ketenimine intermediates, which are formed by the reaction of triphenylalkylidenephosphorane and 6-vinylcyclo-hepta-1,3,5-isocyanate, is described. 10-Alkyl-2,7-methanoaza[10]annulenes were prepared by basic hydrolysis of the carboalkoxyaza[10]annulenes and decarboxylation of the acid intermediates. In the same manner, 10-(N-alkyl(or aryl))-2,7-methanoaza[10]annulenes were prepared from the reaction of the isocyanate and N-alkyl(or aryl)iminotriphenylphosphorane via electrocylic ring-closure of carbodiimide intermediate.

• Archives of Pharmacal Research
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• 제26권1호
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• pp.15-20
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• 2003

Two quinazolone alkaloids, (+)-febrifugine (1) and isofebrifugine (2), along with three coumarin derivatives, 6-hydroxy coumarin (3), skimmin (5), and $umbelliferone-7-O-{\alpha}-L-rhamnopyranosyl(1{\rightarrow}4)-{\beta}-D-glucopyranoside$ (6), were isolated from the roots of Hydrangea chinensis. Compound 6 is a new compound. In addition, umbelliferone (4), linoleic acid (7), two steroidal glycosides (8, 9), three furfural derivatives (10-12), and butyl-$\beta$-D-fructofuranoside (13) were isolated from the leaves of the same plant. The structures of all isolates were elucidated by spectral methods.

• Archives of Pharmacal Research
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• 제21권5호
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• pp.599-609
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• 1998

In search for new antitumor agents, twelve 6-aziridinylbenzimidazole derivatives were synthesized and their cytotoxicities were tested against three cancer cell lines (mouse lymphocytic leukemia P388 and B16, and human gastric carcinoma SNU-16). From 4-amino-3-nitrotoluene as the starting material, 2-(acetoxymethyl)benzimidazoles (5a-d) were obtained by Phillips reaction. These benzimidazoles were then reacted with Fremy's salt to give a mixture of three 2-(acetoxymethyl) (8a-c) and four 2-(hydroxymethyl)benzimidazole-4,7-diones (9a-d). Addition of these quinones with aziridine afforded 6-aziridinyl-2-(acetoxymethyl) (10a-c) and 6-aziridinyl-2-(hydroxymethyl)benzimidazole-4,7-diones (11a-d). Utilizing 2-(hydroxymethyl)benzimidazole-4,7-diones (9b,d), esters 10d and 13e-h were prepared by the sequential reactions of esterification and addition. The synthesized compounds show potent cytotoxicity against all of three cell lines tested. The cytotoxicities of 10a-d or 11a-d against SNU-16 were wuperior to those of 13e-h, and were equal to or slightly higher than that of mitomycin C. compounds 11a-d were slightly more cytotoxic than 10a-d in all cell lines tested.

• Bulletin of the Korean Chemical Society
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• 제34권5호
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• pp.1349-1354
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• 2013

Twenty two new 5-fluorouracil (5-FU) derivatives, 2-butoxy-4-substituted 5-fluoropyrimidines, were synthesized and characterized by IR, $^1H$ NMR, MS, HRMS. All compounds were preliminarily evaluated by MTT assay on human liver BEL-7402 cancer cell line in vitro. Ten compounds were selected to test their cytotoxic activity against A549, HL-60 and MCF-7 cancer cell lines in vitro. These compounds were more sensitive to BEL-7402 than other cell lines, particularly, cytotoxic activity of compounds 6b, 6d-f, 6p, 6s-u were in sub-micromolar scale. The highest cytotoxic potency against A549, HL-60 and MCF-7 was shown by 2-butoxy-4-chloro-5-fluoropyrimidine (5) with $IC_{50}$ values of 0.10, 1.66 and $0.59{\mu}M$, respectively. Compounds 6d and 6e were effective against MCF-7 with $IC_{50}$ $9.73{\mu}M$ and HL-60 with $IC_{50}$ $8.83{\mu}M$, respectively.