• 제목/요약/키워드: Pyrrole

검색결과 222건 처리시간 0.024초

전도성 복합필름의 기상중합과 특성에 대한 연구 (Studies on the Preparation of Conducting Composite Film by a Vapor Phase in situ Polymerization)

  • 박준서;박장우
    • 공업화학
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    • 제10권6호
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    • pp.902-906
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    • 1999

  • 메틸셀루로스를 호스트고분자로 하고 copper(II) percolate를 산화제로 사용하여 기상상태에서 직접중합방법으로 전도성 복합필름을 합성하였다. 필름으로서 우수한 성형성과 기계강도를 갖고 있는 메틸셀루로즈는 PVA와 키토산과는 달리 피롤에 대하여 높은 친화성을 나타내어서 기상중합시 호스트고분자로 적합하였다. 기상중합법으로 합성된 폴리피롤은 복합재료 내에서 전도성네트워크를 형성하여 전도성 복합필름의 전기전도도는 $10^{-1}-10^{-7}S/cm$를 나타내었다. 피롤이 호스트고분자 내에서의 폴리피롤로 중합이 되는 정도를 UV-vis분광계로 확인하였다. 전도성 복합필름의 전기전도도와 기계강도는 산화제의 농도와 합성시간에 크게 의존하였다. TGA분석결과는 호스트고분자 내에 형성된 폴리피롤은 복합재료의 열적 안정성에 영향을 미치지 않는다. 전자현미경 분석결과 폴리피롤이 복합재료 내에 균일하게 침투하여 분산되어 있음을 나타내었다. DMA를 사용하여 폴리피롤과 호스트고분자와의 상용성을 조사하였으며 dynamic mechanical analysis(DMA) 분석결과 복합재료 내에서 폴리피롤의 함량이 증가되면서 상용성이 점진적으로 저하되었다.

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Dipyrrolylbenzene들의 합성에 관한 연구 (A Study on the Synthesis of Dipyrrolylbenzenes)

  • 정대일;변석인;송현애;이도훈;김윤영;이용균;박유미;최순규;한정태
    • 생명과학회지
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    • 제13권6호
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    • pp.836-842
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    • 2003

  • 1,2-phenylenediamino과 2,5-dimethoxytetrahydro- furan을 빙초산 용매하에서 1-(2-aminophenyl)- pyrrole 5를 합성하였다. 1,3-phenylenediamine과 2,5-dimethoxytetrahydrofuran을 빙초산을 사용하여 1-(3-aminophenyl)pyrrole 7과 1,3-dipyrrolyl-benzene 8을 합성하였다. 1,4-phenyl-enediamine과 2,5-dimethoxytetrahydrofuran을 빙초산을 사용하여 1,4-dipyrrolylbenzene 10을 합성하였다. 1,2-phenylenediamine, 1,3-phenylenediamine 그리고 1,4-phenyl-enediamine과 2,5-dimethoxytetra- hydrofuran을 (가) 빙초산 대신, (나) 용매없이, (다) acrylic acid, (라) silica gel, (마) acrylic acid와 silicagel, 그리고 (바) silica gel과 acetic acid를 사용하여 각각 반응시켜 그에 상응하는 amino-phenylpyrroles 5, 7과 dipyrrolylbenzenes 8, 10을 합성하였다. 여러 가지 방법 중 (마) silicagel과 acetic acid를 사용한 경우에 dipyrrolylbenzenes 8, 10의 합성에 관한 반응성이 가장 좋았다. 또한 dicarbazolylbenzene을 합성하기 위한 전단계로 9-phenylcarbazole 11을 합성하였다.

  • https://doi.org/10.5352/JLS.2003.13.6.836 인용 PDF KSCI

Selective Determination of Serotonin on Poly(3,4-ethylenedioxy pyrrole)-single-walled Carbon Nanotube-Modified Glassy Carbon Electrodes

  • Kim, Seul-Ki;Bae, Si-Ra;Ahmed, Mohammad Shamsuddin;You, Jung-Min;Jeon, Seung-Won
    • Bulletin of the Korean Chemical Society
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    • 제32권4호
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    • pp.1215-1220
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    • 2011

  • An electrochemically-modified electrode [P(EDOP-SWNTs)/GCE] was prepared by electropolymerization of 3,4-ethylenedioxy pyrrole (EDOP) single-walled carbon nanotubes (SWNTs) on the surface of a glassy carbon electrode (GCE) and characterized by SEM, CV, and DPV. This modified electrode was employed as an electrochemical biosensor for the selective determination of serotonin concentrations at pH 7.4 and exhibited a typical enhanced effect on the current response of serotonin with a lower oxidation overpotential. The linear response was in the range of $1.0{\times}10^{-7}$ to $1.0{\times}10^{-5}$ M, with a correlation coefficient of 0.998 on the anodic current. The lower detection limit was calculated as 5.0 nM. Due to the relatively low currents and difference of potentials in the electrochemical responses of uric acid (UA), ascorbic acid (AA), and dopamine (DA), the modified electrode was a useful and effective sensing device for the selective and sensitive serotonin determination in the presence of UA, AA, and DA.

  • https://doi.org/10.5012/bkcs.2011.32.4.1215 인용 PDF KSCI

Pyrrole-Derivative of Chalcone, (E)-3-Phenyl-1-(2-Pyrrolyl)-2-Propenone, Inhibits Inflammatory Responses via Inhibition of Src, Syk, and TAK1 Kinase Activities

  • Yang, Sungjae;Kim, Yong;Jeong, Deok;Kim, Jun Ho;Kim, Sunggyu;Son, Young-Jin;Yoo, Byong Chul;Jeong, Eun Jeong;Kim, Tae Woong;Han Lee, In-Sook;Cho, Jae Youl
    • Biomolecules & Therapeutics
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    • 제24권6호
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    • pp.595-603
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    • 2016

  • (E)-3-Phenyl-1-(2-pyrrolyl)-2-propenone (PPP) is a pyrrole derivative of chalcone, in which the B-ring of chalcone linked to ${\beta}$-carbon is replaced by pyrrole group. While pyrrole has been studied for possible Src inhibition activity, chalcone, especially the substituents on the B-ring, has shown pharmaceutical, anti-inflammatory, and anti-oxidant properties via inhibition of NF-${\kappa}B$ activity. Our study is aimed to investigate whether this novel synthetic compound retains or enhances the pharmaceutically beneficial activities from the both structures. For this purpose, inflammatory responses of lipopolysaccharide (LPS)-treated RAW264.7 cells were analyzed. Nitric oxide (NO) production, inducible NO synthase (iNOS) and tumor necrosis factor-${\alpha}$ (TNF-${\alpha}$) mRNA expression, and the intracellular inflammatory signaling cascade were measured. Interestingly, PPP strongly inhibited NO release in a dose-dependent manner. To further investigate this anti-inflammatory activity, we identified molecular pathways by immunoblot analyses of nuclear fractions and whole cell lysates prepared from LPS-stimulated RAW264.7 cells with or without PPP pretreatment. The nuclear levels of p50, c-Jun, and c-Fos were significantly inhibited when cells were exposed to PPP. Moreover, according to the luciferase reporter gene assay after cotransfection with either TRIF or MyD88 in HEK293 cells, NF-${\kappa}B$-mediated luciferase activity dose-dependently diminished. Additionally, it was confirmed that PPP dampens the upstream signaling cascade of NF-${\kappa}B$ and AP-1 activation. Thus, PPP inhibited Syk, Src, and TAK1 activities induced by LPS or induced by overexpression of these genes. Therefore, our results suggest that PPP displays anti-inflammatory activity via inhibition of Syk, Src, and TAK1 activity, which may be developed as a novel anti-inflammatory drug.

  • https://doi.org/10.4062/biomolther.2016.027 인용 PDF KSCI

Pyrrole derivatives from Lycium chinense

  • Chin, Y.W.;Kim, J.
    • 대한약학회:학술대회논문집
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    • 대한약학회 2000년도 NEW STRATEGY FOR DRUG DEVELOPMENT IN POST-GENOMIC ERA(대한약학회)
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    • pp.220.3-221
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    • 2000

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