Please use this identifier to cite or link to this item: http://113.161.190.196:8080/thuvienso/handle/123456789/1027
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dc.contributor.authorTesta, Bvi
dc.contributor.authorTurski, Lvi
dc.date.accessioned2015-02-04T03:40:10Z-
dc.date.available2015-02-04T03:40:10Z-
dc.date.issued2006vi
dc.identifier.isbn978-1-58603-703-1vi
dc.identifier.urihttp://10.0.16.20:8080/dspace/handle/DLU123456789/35108vi
dc.identifier.urihttp://192.168.1.40:8080/thuvienso/handle/123456789/1027-
dc.description.abstractToday, biologists and medicinal chemists realize that there is a strong relationship between pharmacodynamic (what the drug does to the organism) and pharmacokinetic (what the organism does to the drug) effects. A significant contributing factor to the evolution in drug discovery was the methodological and technological revolution with the advent of combinatorial chemistry, high-throughput screening and profiling, and in silico prediction of target-based activity and ADMET (absorption, distribution, metabolism, excretion and toxicity) properties. High-throughput screening and in silico methodsvi
dc.language.isoenvi
dc.publisherIOS Pressvi
dc.subjectVirtualvi
dc.subjectComputervi
dc.titleVirtual ADMET Assessment in Target Selection and Maturationvi
dc.typeBookvi
Appears in Collections:Sách, Giáo trình điện tử - Tiếng Anh

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