• 한국잡초학회지
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• 제12권2호
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• pp.173-182
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• 1992

해바라기의 상대억제작용(相對抑制作用)(타감작용(他感作用), Allelopathy) 및 천연제초제(天然除草劑)로서의 개발가능성(開發可能性)에 관한 시험(試驗)을 1988-1991년(年)에 걸쳐 국제미작연구소(國際米作硏究所) 농학(農學), 생화학부(生化學部) 및 국립(國立)필리핀 대학교(大學校) 화학과(化學科) 천연물(天然物) 연구실(硏究室)에서 수행(遂行)하여 얻은 결과중(結果中) 상대억제작용성(相對抑制作用性) 해바라기 근분비물질(根分泌物質)의 생물검정(生物檢定) 및 상대억제작용물질(相對抑制作用物質)(Allelochemicals)의 HPLC 분석결과(分析結果)는 다음과 같다. 1. 해바라기 근분비물질(根分泌物質)의 산(酸) 및 중성분획물질(中性分劃物質)을 생물검정재료(生物檢定材料)로 사용한 피 (Echinochloa colona (L.) Link 및 무 (Raphanus sativus L.)의 발아(發芽)가 유의성(有意性)있는 억제(抑制)를 보인 반면 알칼리 및 수용성분획(水溶性分劃)에서는 억제작용(抑制作用)이 나타나지 않았다. 2. 피의 경우 해 바라기 근분비물질(根分泌物質)의 분획물질(分劃物質) $10{\mu}l$ 농도(濃度)에서부터 유의적(有意的)인 생장억제(生長抑制)가 인정(認定)되었으며 지상부(地上部) 신장억제(伸張抑制)보다 지하부(地下部) 신장억제(伸張抑制)가 산(酸) 및 중성분획(中性分劃)에서 더 강하게 나타났다. 3 무의 경우 농도(濃度)에 관계없이 지상(地上) 및 지하부(地下部) 신장억제(伸張抑制)가 산(酸) 및 중성분획(中性分劃)에서 각각 높게 나타났다. 4. 생물검정(生物檢定)에서 강한 상대억제작용(相對抑制作用)을 보인 산성분획물질(酸性分劃物質)의 HPLC분석결과(分析結果) hydroquinone, ${\beta}$-resorcyclic acid, vanillic acid, caffeic acid, salicylic acid, quercetin 등의 물질(物質)이 확인(確認)되었다. 한편, 중성분획물질(中性分劃物質)에서는 Hydroquinone, gentisic acid, ${\beta}$-resorcyclic acid, vanillic acid, caffeic acid, ferulic acid, quercetin 등이 각각 동정(同定)되었다.

• 한국환경성돌연변이발암원학회지
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• 제22권2호
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• pp.90-96
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• 2002

Benzene is a widespread human carcinogen, inducing leukemia and hematotoxicity. Exposure to benzene metabolites has been shown to cause genetic damage, including aneusomy and chromosome aberrations. Fluorescence in situ hybridization(FISH) procedure was used to determine if the benzene metabolite, 1, 2, 4-benzenetriol(BT), hydroquinone(HQ) and trans, trans-muconic acid(t,t-MA) induced specific chromosomal change in HL-60 cells. Treatment with BT, HQ and t,t-MA resulted in the induction of monosomy 8 and 21 in HL-60 cells in a dose-dependent manner. All of these metabolites also induced trisomy 8 and 21, but no correlation between frequencies of trisomy and concentration was found. Translocations between chromosome 8 and another unidentified chromosome ［t(8:\ulcorner)］, and between chromosome 21 and another unidentified chromosome ［t(8:21)］ were found. However, translocation between chromosome 8 and 21 ［t(8:21)］ was not found. Results indicate that the benzene metabolites, BT, HQ and t,t-MA, induce chromosome specific numerical and structural aberrations, and the fluorescence in situ hybridization (FISH) approach may be a useful and powerful technique for detection of aneuploidy.

• 한국식품과학회지
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• 제22권6호
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• pp.618-624
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• 1990

사과(Jona gold)로부터 추출한 polyphenol oxidase와 polyphenol 화합물인 catechol, hydroquinone, homocatechol, hydroxyhydroquinone 그리고 pyrogallol 용액과 반응시켜 얻어진 사과효소 갈변반응 생성물에 대한 항돌연변이원성 효과를 검토하였다. SOS spot test와 SOS chromotest에 사용된 균주는 E. coli PQ37/plasmid pKM101 균주이며 spot test에서 위 다섯 종류의 시료 모두 갈변용액의 농도를 증가시켜 줌에 따라서 mitomycin C(MMC), 4-nitroquinoline-1-oxide(4NQO), 그리고 N-methyl-N'-nitro-N-nitrosoguanidine(MNNG) 등의 발암물질들에 대해서 강한 억제활성을 나타내었다. 한편, SOS chromotest에서도 발암물질의 종류에 따라 차이는 있으나 갈변용액의 농도증가에 따라 MMC, MNNG, 4 NQO 그리고 3-amino-1,4-dimethyl-5H-pyrido-(4,3-b) indol (Trp-P-1) 등에 대해서 강한 억제활성을 나타내었다.

• 한국환경보건학회지
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• 제23권3호
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• pp.121-129
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• 1997

This study was performed to delineate the removal phenol in solutions using of ozone, ozone/$H_2O_2$ and ozone/GAC. The disinfection by-product of phenol by ozonation, hydroquinone, was analyzed and it's control process was investigated. The followings are the conclusions that were derived from this study. 1. The removal efficiency of phenol by ozonation was 58.37%, 48.34%, 42.15%, and 35.41% which the initial concentration of phenol was 5 mg/l, 10 mg/l, 15 mg/l, and 20 mg/l, respectively. 2. The removal efficiency of phenol by ozonation was 42.95% at pH 4.0 and 69.39% at pH 10, respectively. The removal efficiencies were gradually increased, as pH values were increased. 3. With the ozone/$H_2O_2$ combined system, the removal efficiency of phenol was 72.87%. It showed a more complete degradation of phenol with ozone/$H_2O_2$ compared with ozone alone. 4. When ozonation was followed by filtration on GAC, phenol was completely removed. 5. Oxidation, if carried to completion, truly destroys the organic compounds, converting them to carbon dioxide. Unless reaction completely processed, disinfection by-products would be produced. To remove them, ozone/GAC treatment was used. The results showed that disinfection by-product of phenol by ozonation, hydroquinone, was completely removed. These results suggested that ozone/GAC should also be an appropriate way to remove phenol and its by-product.

• 전기화학회지
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• 제6권2호
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• pp.130-133
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• 2003

3,4-dihydroxybenzoic acid(3,4-DHBA)를 전기화학법으로 유리탄소 전극 위에 중합하여 GC/p-3,4-DHBA형의 전극을 제작한 후 이 전극을 도파민으로 재 수식한 전극을 제작하였다. 이 때 고분자 피막 상에 카르복시기와 도파민의 아민 기간에 짝 짓기 반응은 1-(3-dimethylaminopropyl)-3-ethyl carbodiimide hydrochloride(EDC)의 존재하에서 진행되었다. 이 반응과정에서 반응한 도파민의 양은 수정판 분석기(quartz crystal analyzer:QCA)에 의하여 결정하였으며 그때 전극형태는 QCA(Au)/p-3,4-DHBA-dopamine이었다. 이 전극의 표면은 o-퀴논부분을 갖고 있어서 티탄이온에 선택성이 큰 특성을 갖고 있다. 이 전극의 산화환원과정은 $hydroquinone = quinone +2H^+2e^-$으로 두 개의 강한 파와 두개의 약한 파가 CV과정에서 관찰되었다. 이 수식전극으로 Ti(IV)이온을 $4.13\times10^{-5} gcm^{-2}$만큼 포집할 수가 있었다. 이 수식 전극으로 $5.25\times10^{-4}M$에서 $5.25\times10^{-8}M$농도범위까지 정량 할 수 있는 상관계수가 0.997인 검정선을 얻었다.

• Archives of Pharmacal Research
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• 제22권4호
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• pp.335-339
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• 1999

The oxidation-reduction potentials of cosmetic raw materials, showing tyrosinase inhibitory action, and phenolic compounds structurally similar to L-tyrosine were determined by cylcic voltammetry. The voltammograms obtained could be classified ito 4 patterns (patterns 1-4). Patterns 1, characterized by oxidation and reduction peaks as a pair, was observed with catechol, hydroquinone or phenol, and pattern 2 exhibiting another oxidation peak in addition to oxidation and reduction peaks as a pair was found with arbutin, kojic acid, resorcinol, methyl p-hydroxybenzoate and L-tyrosine as the substrate of tyrosinase. Pattern 3 with an independent oxidation peak only was expressed by L-ascorbic acid, and pattern 4 with a reduction peak only at high potentials, by hinokitiol. The tyrosinase inhibitory activity of these compounds was also evaluated using the 50% inhibitory concentration ($IC_{50}$) and the inhibition constant (Ki) as parameters. Hinokitiol, classified as patterns 4, showed the highest inhibitory activity (lowest $IC_{50}$ and Ki). Hydroquinone showing the second highest activity belonged to pattern 1, which also included compounds exhibiting pattern 2 was relatively low with Ki values being in the order of 10-4 M. Although there was no consistent relationship between oxidation-reduction potentials and tyrosinase inhibitory action, the voltammetry data can be used as an additional index to establish the relationship between the structure and the tyrosine inhibitory activity.

• Bulletin of the Korean Chemical Society
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• 제17권1호
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• pp.11-15
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• 1996

A series of poly(1,4-phenylene terephthalates) with pendant NLO chromophores was prepared by the solution polycondensation of 2,5-NLO chromophore substituted terephthalic acid with hydroquinone. The polymers obtained gave satisfactory NMR and elemental analysis results when taking into account their expected structures and the inherent viscosity value proved the polymeric character of all polymers. DSC, optical polarizing microscopy and WAXS studies revealed that none of these polymers exhibited liquid crystalline mesophases. Preliminary results on NLO properties of these polymers showed a surprisingly large second harmonic signal relative to a Y-cut quartz plate.

• 공업화학
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• 제5권3호
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• pp.517-523
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• 1994

DGEBA(diglycidyl ether of bisphenol A)/MDA(4,4'-methylene dianiline)/SN(succinonitrile)/HQ(hydroquinone)계의 경화반응 속도론 및 메카니즘을 연구하였다. SN과 HQ는 반응성 첨가제와 촉매로 도입하였다. 경화반응 속도론은 DSC 분석에 의해 Kissinger equation과 fractional-life법을 이용하여 연구하였다. DGEBA/MDA/SN 계의 활성화에너지와 반응차수는 SN의 함량에 관계없이 거의 일정하였고, 촉매로써 HQ가 첨가됨으로 인해 활성화 에너지와 반응시작온도가 낮아졌다. 이들 계의 반응 메카니즘을 고찰하기위하여 SN의 함량에 따라 FT-IR을 측정하였다. 그리고, SN:HQ의 혼합비는 4:1이었다. Diamine으로 경화되는 에폭시 수지의 경화반응 메카니즘은 primary amine-epoxy 반응, secondary amine-epoxy 반응, epoxy-hydroxyl 반응이 일어나는 것으로 알려져 있다. DGEBA/MDA/SN/HQ 계에서는 HQ의 hydroxyl 기가 epoxy 및 amine과 결합하여 전이상태를 형성하여 epoxide ring을 빠르게 개환시켜줌으로써 amine-epoxy반응이 쉽게 일어남을 알았다.

• 한국결정학회지
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• 제2권2호
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• pp.13-21
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• 1991

50% terephthaloyl chloride(TPA)와 50%(1-phenylethyl) hydroquinone(PEHQ)으로부터 합성된 열 액정폴리에스터 poly(1-phenylethyl-p-phenylene-terephthalate)의 chalk conformation 및 packing 상태를 X-선 회절법을 이용하여 해석하였다. 단위세포상수는 a=12.77 A, b=10.17 A(unlque axis), c=12.58 A (fiber axis), β=90.1°, 그리고 공간군은 P2l 이고 단사정계이며 Z:4 이었다. 미세구조는 주쇄상의 Phenyl-COO 그리고 COO-Phenyl 평면간의 그리고 주축과 측쇄간의 torsion angle 들을 중심으로 37개의 회절반점에 대해 Linked Atom Least Square(LALS) 방법을 이용하여 해석하였으며, 1-phenylethyl 치환체는 ortho-와 met a위치에 각각 확률적으로 0.5의 가중치를 부여함에 의해 구조적으로 모델링 되었다. 주쇄상의 Phenyl-COO그리고 Phenyl-COO평면간의 torsion angle은 각각 -6.1°와 65.6°로 주어졌으며 결국 주축상의 Phenol 평면들은 서로 59.5°로 엇갈려 주축을 형성하고 있음을 알 수 있었다. (단 ester, COO-, 기는 평면으로 가정되었다.)

• Biomolecules & Therapeutics
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• 제26권4호
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• pp.417-423
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• 2018

Extracellular interleukin 1 alpha (IL-$1{\alpha}$) released from keratinocytes is one of the endpoints for in vitro assessments of skin irritancy. Although cells dying via primary skin irritation undergo apoptosis as well as necrosis, IL-$1{\alpha}$ is not released in apoptotic cells. On the other hand, active secretion has been identified in interleukin-1 receptor antagonist (IL-1ra), which was discovered to be a common, upregulated, differentially-expressed gene in a microarray analysis performed with keratinocytes treated using cytotoxic doses of chemicals. This study examined whether and how IL-1ra, particularly extracellularly released IL-1ra, was involved in chemically-induced keratinocyte cytotoxicity and skin irritation. Primary cultured normal adult skin keratinocytes were treated with cytotoxic doses of chemicals (hydroquinone, retinoic acid, sodium lauryl sulfate, or urshiol) with or without recombinant IL-1ra treatment. Mouse skin was administered irritant concentrations of hydroquinone or retinoic acid. IL-1ra (mRNA and/or intracellular/extracellularly released protein) levels increased in the chemically treated cultured keratinocytes with IL-$1{\alpha}$ and IL-$1{\beta}$ mRNAs and in the chemically exposed epidermis of the mouse skin. Recombinant IL-1ra treatment significantly reduced the chemically-induced apoptotic death and intracellular/extracellularly released IL-$1{\alpha}$ and IL-$1{\beta}$ in keratinocytes. Collectively, extracellular IL-1ra released from keratinocytes could be a compensatory mechanism to reduce the chemically-induced keratinocyte apoptosis by antagonism to IL-$1{\alpha}$ and IL-$1{\beta}$, suggesting potential applications to predict skin irritation.