• 제목/요약/키워드: Quinoline

검색결과 228건 처리시간 0.024초

A Study of Antibacterial Activity of Some Novel 8-Methoxy-4-methyl-quinoline Derivatives

  • Singh, Sheoraj;Kumar, Vikas;Kumar, Ashok;Sharma, Shalabh;Dua, Piyush
    • Bulletin of the Korean Chemical Society
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    • 제31권12호
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    • pp.3605-3610
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    • 2010
  • In the present study, some quinoline derivatives have been synthesized like 8-methoxy-4-methyl-2-amino-(3'-chloro-2'-oxo-4'-substituted aryl-1'-azetidinyl)quinolines 8-12 and 8-methoxy-4-methyl-2-amino-(2'-substituted aryl-4'-oxo-1',3'-thiazolidin-3'-yl) quinolines 13-17 from 8-methoxy-4-methyl-2-(substituted arylidenyliminoamino)-quinolines 3-7. The structural assignments of these compounds were based on spectral (IR, $^1H$-NMR, Mass) and elemental (C, H, N) analysis. Further, these compounds were evaluated for antibacterial activity against various bacterial strains. Three compounds 10, 11 and 16 were found to exhibit potent antibacterial activity as compared to the standard drug amphicillin.

A novel quinoline derivative with high affinity for the translocator protein

  • Kwon, Young-Do;Kim, Hee-Kwon
    • 대한방사성의약품학회지
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    • 제1권2호
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    • pp.95-97
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    • 2015
  • The translocator protein (TSPO) is one of the important targets for Positron Emission Tomography (PET) imaging because it is associated with brain cancer, stroke, and neurodegeneration. Recently, a novel quinoline compound with high affinity agent for the translocator protein has been developed. In this highlight review, major studies for the quinoline compound are described.

Synthesis and In Vitro Cytotoxicity of 4-Alkyl- or 4-Arylaminosubstituted Cyclopenta[c]quinoline Derivatives

  • Lee, Hee-soon;Lee, Jee-man;Yang, Sung-Il
    • Archives of Pharmacal Research
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    • 제24권5호
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    • pp.385-389
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    • 2001
  • Twelve 4-substituted cyclopenta[c]quinoline derivatives were synthesized and evaluated in vitro cytotoxicity against four human cancer cell lines (HOP62, SK-OV-3, MD-MB-468 and T-47D). The compounds 6c and 6e bearing p-anisidine and pyrrolidine side chain were more active than the others.

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INHIBITION OF LPS-INDUCED p38 ACTIVATION AND iNOS EXPRESSION BY 2-AMINO-3-METHYLIMIDAZO[4,5-f]QUINOLINE

  • Jeon, Young-Jin
    • 한국독성학회:학술대회논문집
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    • 한국독성학회 2002년도 Current Trends in Toxicological Sciences
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    • pp.100-100
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    • 2002
  • 2-amino-3-methylimidazo[4,5-f]quinoline (IQ), a heterocyclic amine, significantly inhibits nitric oxide (NO) production in lipopolysaccharide (LPS)-stimulated macrophages. The decrease in NO production was found to correlate well with a decrease in iNOS mRNA expression as demonstrated by Northern blot analysis.(omitted)

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An Efficient Synthesis of Substituted Quinolines via Indium(III) Chloride Catalyzed Reaction of Imines with Alkynes

  • Zhu, Mei;Fu, Weijun;Xun, Chen;Zou, Guanglong
    • Bulletin of the Korean Chemical Society
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    • 제33권1호
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    • pp.43-47
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    • 2012
  • An efficient synthetic method for the preparation of quinolines through indium(III) chloride-catalyzed tandem addition-cyclization-oxidation reactions of imines with alkynes was developed. The processes can provide a diverse range of quinoline derivatives in good yields from simple imines and alkynes.

콜타르 유분 중에 함유된 인돌의 고순도 정제 - 용액 결정화에 의한 인돌 유사 비점 혼합물의 분리 - (High-Purity Purification of Indole Contained in Coal Tar Fraction - Separation of Close Boiling Mixtures of Indole by Solute Crystallization -)

  • 김수진;강호철;정화진
    • 공업화학
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    • 제21권2호
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    • pp.238-241
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    • 2010
  • 콜타르 유분(유출온도범위: $240{\sim}265^{\circ}C$)으로부터 추출-증류의 조합에 의해 회수한 54.3 wt% 인돌 유출액(유출온도범위 $250{\sim}255^{\circ}C$)을 원료로 사용하여 용액 결정화 조작을 행해 인돌의 고순도 정제를 검토했다. 원료 유출액은 8성분(quinoline, iso-quinoline, indole, quinaldine, 1-methylnaphthalene, 2-methylnaphthalene, biphenyl, phenyl ether)으로 구성되어 있다. 결정화 조작의 용매로서는 노말헥산을, 냉매로서는 메탄올 수용액(50 : 50 vol%)을 각각 사용하였으며, 결정화 장치로서는 재킷이 부착된 pyrex제 유리 회분 교반기를 사용했다. 결정화 온도와 용매/원료의 초기 체적비의 증가는 인돌의 순도를 향상시켰으나, 역으로 수율을 저하시켰다. 석출된 결정의 세정조작 없이, 노말헥산을 용매로 사용한 용액 결정화 조작에 의해 고순도(99.3 wt%)의 인돌을 고수율(50%)로 회수할 수 있었다.

Synthesis and Properties of Diarylamino-Substituted Linear and Dendritic Oligoquinolines for Organic Light-Emitting Diodes

  • Lee, Ho-Joon;Xin, Hao;Park, Seong-Min;Park, Seog-Il;Ahn, Taek;Park, Dong-Kyu;Jenekhe, Samson A.;Kwon, Tae-Woo
    • Bulletin of the Korean Chemical Society
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    • 제33권5호
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    • pp.1627-1637
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    • 2012
  • The coupling reaction between 5-bromo-3-phenylbenzo[c]isoxazole and diphenylamine followed by further condensation with a mono-, di- or ter-acetyl aromatic compound in the presence of diphenyl phosphate at $145^{\circ}C$ gave a novel asymmetric diarylquinolines, oligoquinolines with diphenylamine endgroups, and a first generation quinoline dendrimer in 41-82% isolated yield. The electrochemical and photophysical properties of the oligoquinolines were characterized by cyclic voltammograms (CVs) and spectroscopy. All the quinolines emit bright sky blue light due to charge transfer from quinoline group to diphenly amine with very high quantum efficiency (> 90%). Organic light-emitting diodes (OLEDs) were fabricated using these quinolines as emitting materials. Among different device architectures explored, OLEDs with a structure of ITO/PEDOT (40 nm)/TAPC (15 nm)/D-A quinoline (40 nm)/TPBI (30 nm)/LiF (1 nm)/Al using TAPC as an electron blocking layer and TPBI as a hole blocking layer gave the best performance. A high external quantum efficiency in the range of 1.2-2.3% were achieved in all the quinolines with the best performance in BBQA(5). Our results indicate diarylamino-substituted oligoquinoline and dendrimer are promising materials for OLEDs applications.

회분 병류 5단 평형추출에 의한 모델 콜타르 유분 중에 함유된 Indole의 분리 및 회수 (Separation and Recovery of Indole from Model Coal Tar Fraction by Batch Cocurrent 5 Stages Equilibrium Extraction)

  • 김수진;전용진;정화진
    • 공업화학
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    • 제18권2호
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    • pp.168-172
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    • 2007
  • 회분 병류 5단 평형추출에 의해 4종류의 질소고리화합물[indole(In), quinoline(Q), iso-quinoline(iQ), quinaldine(Qu)], 3종류의 2환 방향족화합물[1-methylnaphthalene(1MN), 2-methylnaphthalene(2MN), dimethyl naphthalene(DMN)], biphenyl과 phenyl ether로 구성된 모델 혼합물로부터 In의 분리를 검토했다. 본 연구의 원료로서 사용된 모델 혼합물은 콜타르 유분(유출온도범위: $240{\sim}265^{\circ}C$)을 구성하고 있는 성분 및 조성을 고려하여 작성했다. 추출용매로서는 Formamide 수용액을 사용했다. 4단 평형추출을 통해 In을 99% 이상 회수할 수 있었다. 5단 평형추출을 통해 얻어진 DMN을 기준성분으로한 In의 선택도는 63~118의 범위를 나타냈다. 본 연구를 통해 얻어진 실험적 결과와 이전의 연구결과를 이용하여 콜타르 중에 함유된 In의 분리 및 회수공정을 검토했다.