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Effect of Chemical Doping and Ion Implantation on Cond uctivity of Poly(p-phenylene vinylene) Derivatives 被引量:1
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作者 LI Bao-ming WU Hong-cai LIU Xiao-zeng LI Xiao-qi GAO Chao 《Semiconductor Photonics and Technology》 CAS 2005年第3期188-191,共4页
The surface conductivity of poly [ 2-methoxy-5-(3'-methyl) butoxy]-p-phenylene vinylene (PMOMBOPV) films doped with FeCl3 and H2SO4 by chemical method and implanted by N^+ ions was studied and the comparison of ... The surface conductivity of poly [ 2-methoxy-5-(3'-methyl) butoxy]-p-phenylene vinylene (PMOMBOPV) films doped with FeCl3 and H2SO4 by chemical method and implanted by N^+ ions was studied and the comparison of environmental stability of conductive behavior was also investigated. The energy and dose of N^+ ions were in the rang 15~35 keV and 3. 8×10^15~9. 6×10^16 ions/cm^2, respectively. The conductivity of PMOMBOPV film was enhanced remarkably with the increases of the energy and dose of N^+ ions. For example, the conductivity of PMOMBOPV film was 3. 2×10^-2S/cm when ion implantation was performed with an energy of 35 keV at a dose of 9. 6 × 10^14 ions/cm^2 , which was almost seven orders of magnitude higher than that of film unimplanted. The environmental stability of conductive behavior for ionimplanted film was much better than that of chemical doped films. Moreover, the conductive activation energy of ion-implanted films was measured to be about 0.17 eV. 展开更多
关键词 Ion implantation Chemical doping Poly[2-methoxy-5-3-methyl)butoxy]-p-phenylene vinylene Surface conductivity Conductive activation energy
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Screening of chemokine receptor CCR4 antagonists by capillary zone electrophoresis 被引量:1
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作者 Zhe Sun Lin-Jie Tian +3 位作者 Qian Lin Xiao-Mei Ling Jun-Hai Xiao Ying Wang 《Journal of Pharmaceutical Analysis》 SCIE CAS 2011年第4期264-269,共6页
CC chemokine receptor 4(CCR4)is a kind of G-protein-coupled receptor,which plays a pivotal role in allergic inflammation.The interaction between 2-(2-(4-chloro-phenyl)-5-{[(naphthalen-1-ylmethyl)-carbamlyl]-methyl-4-o... CC chemokine receptor 4(CCR4)is a kind of G-protein-coupled receptor,which plays a pivotal role in allergic inflammation.The interaction between 2-(2-(4-chloro-phenyl)-5-{[(naphthalen-1-ylmethyl)-carbamlyl]-methyl-4-oxo-thiazolidin-3-yl)-N-(3-morpholin-4-yl-propyi)-acetamide(S009)and the N-terminal extracellular tail(ML40)of CCR4 has been validated to be high affinity by capillary zone electrophoresis(CZE).The S009 is a known CCR4 antagonist.Now,a series of new thiourea derivatives have been synthesized.Compared with positive control S009,they were screened using ML40 as target by CZE to find some new drugs for allergic inflammation diseases.The synthesized compounds XJH-5,XJH-4,XJH-17 and XJH-1 displayed the interaction with ML40,but XJH-9,XJH-10,XJH-I 1,XJH-12,XJH-13,XJH-14,XJH-3,XJH-8,XJH-6,XJH-7,XJH-15,XJH-16 and XJH-2 did not bind to ML40.Both qualification and quantification characterizations of the binding were determined.The affinity of the four compounds was valued by the binding constant,which was similar with the results of chemotactic experiments.The established CEZ method is capable of sensitive and fast screening for a series of lactam analogs in the drug discovery for allergic inflammation diseases. 展开更多
关键词 Capillary zone electrophoresis CCR4 antagonist 2-(2-(4-chloro-phenyl)-5-{[(naphthalen-1-ylmethyl)-carbamoyl]-methyl}-4-oxo-thiazoli-din-3-yl)-N-(3-morpho-lin-4-yl-propyl)-aceta-mide Interactions Structural modification
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