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20篇 您的检索式:作者名="Velkov T"
    题名 作者 年代 出处 被引量
1Pharmacology of polymyxins: New insights into an 'old' class ofantibiotics显示文摘Velkov T Roberts K D Nation R L 2013Future Microbiol2013,8,6:1
2Structure-activity relationships of polymyxin antibiotics显示文摘Velkov T Thompson P E Nation R L 2009J Med Chem2009,53,5:1
3The RNA-dependent-RNA pol- ymerase, an emerging antiviral drug target for the Hendra virus 显示文摘Velkov T Carbone V Akter J 2014Curr Drug Targets2014,15,1:1
4Colistin and polymyxin B: peas in a pod, or chalk and cheese? 显示文摘Nation RL Velkov T Li J 2014Clin Infect Dis2014,59,1:1
5Structure-activity relationships of polymyxin antibiotics 显示文摘Velkov T Thompson PE Nation R L 2010J MedChem2010,53,5:1
6Characterization of the drug binding specificity of rat liver fatty acid binding protein 显示文摘CHUANG S VELKOV T HORNE J 2008J Med Chem2008,51,13:1
7The antigenic architecture of the hemagglutinin of influenza H5N1 viruses显示文摘Velkov T Ong C Baker M A 2013Mol Immunol2013,56,:1
8Non-ribosomal peptide synthetases as technological platforms for the synthesis of highly modified peptide bioeffectors cyclosporin synthetase as a complex example显示文摘Velkov T Lawen A 2003Biotechnol Annu Rev2003,9,:1
9Pharmacology of polymyxins: new insights into an 'old' class of antibiotics显示文摘Velkov T Roberts KD Nation RL 2013Future Microbiol2013,8,6:1
10The interaction of lipophilic drugs with intestinal fatty acid -binding protein显示文摘VELKOV T CHUANG S WIELENS 1 2005J BioI Chern2005,280,17:1
11The antigenic archi- tecture of the hemagglutiniq of influenza H5N1 viruses显示文摘Velkov T Ong C Baker M A 2013Mol Immunol2013,56,:1
12Pharmacologyof polymyxins:new insights into an ‘old’ class ofantibiotics显示文摘Velkov T Roberts tCD Nation R L 2013Future Microbiol2013,8,6:1
13The specificity of the influenza B virus hemagglutinin re- ceptor binding pocket: what does it bind to? 显示文摘Velkov T 2013J Mol Recognit2013,26,10:1
14Teaching ‘old,polymyxins new tricks: new-generation lipopeptidestargeting gram-negative ‘superbugs,显示文摘Velkov T Roberts KD Nation RL 2014ACS Chem Biol2014,9,5:1
15Characterization of lipophilic drug binding to rat intestinal fatty acid binding protein显示文摘Velkov T Lim M L Home J 2009Molecular and Cellular Biocheroistry2009,326,12:1
16Characterization of the drug binding speciflcity of rat liver fatty acid binding protein显示文摘Chuang S Velkov T Home P 2008Med Chem2008,51,13:1
17Characterization of the drug binding specificity of rat liver fatty acid binding protein显示文摘Chuang S Velkov T Horne J 2008J Med Chem2008,51,13:1
18多黏菌素E和多黏菌素B:一模一样,还是截然不同?显示文摘多黏菌素E和多黏菌素B在体外抗菌活性难分伯仲,但临床上这两种药的静脉制剂的组成不同。多黏菌素B以其活性体(硫酸盐)直接给药,而多黏菌素 E以一种无活性的前体药(甲磺酸盐)给药,即甲磺酸多黏菌素 E(CMS)。CMS须在体内转换成多黏菌素 E才能发挥抗菌作用,但这个过程缓慢且转换不完全。本文总结了CMS/多黏菌素 E和多黏菌素B静脉制剂的主要不同点,如静脉制剂组份、在体内的分布和清除途径等,并着重比较两种形式对临床用药的影响。总的来说,多黏菌素B比CM S/多黏菌素E有更好的临床药理特性,如前者可快速达到并维持有效的血药浓度,且受肾功能影响相对较小。建议同时有多黏菌素 E和多黏菌素B静脉制剂的国家如美国、巴西、马来西亚、新加坡等,开展前瞻性研究比较两者在不同患者及不同种类感染中的有效性和安全性。临床医师在使用两种多黏菌素类时应考虑两者的优劣而加以选用。Nation RL Velkov T Li J 盛滋科 2015中国感染与化疗杂志2015,15,5:1
19Interaction of phthalates and phenoxy acid herbicide environmental pollutants with intestinal intracellular lipid binding proteins显示文摘Carbone V Velkov T 2013Chem Res Toxicol2013,26,8:1
20Characterization of the drug binding specificity of rat liver fatty acid binding protein显示文摘Chuang S Velkov T Home J 2008J Med Chem2008,51,13:1
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