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Titlebook: Drug Design; Methodology, Concept Gerhard Klebe Reference work 2013 Springer-Verlag Berlin Heidelberg 2013 Drug Design.Hit-to-lead optimiza

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發(fā)表于 2025-3-21 16:20:07 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書(shū)目名稱(chēng)Drug Design
副標(biāo)題Methodology, Concept
編輯Gerhard Klebe
視頻videohttp://file.papertrans.cn/284/283058/283058.mp4
概述Unique reference work on the subject of drug design.Full colours throughout.Intelligibly written and illustrated containing over 100 computer graphics.Including an index of about 5,000 items
圖書(shū)封面Titlebook: Drug Design; Methodology, Concept Gerhard Klebe Reference work 2013 Springer-Verlag Berlin Heidelberg 2013 Drug Design.Hit-to-lead optimiza
描述Unique work on structure-based drug design, covering multiple aspects of drug discovery and development. Fully colored, many images, computer animations of 3D structures (these only in electronic form). Makes the spatial aspects of interacting molecules clear to the reader, covers multiple applications and methods in drug design. Structures by mode of action, no therapeutic areas. Of high relevance for academia and industrial research. Focus on gene technology in drug design, omics-technologies computational methods experimental techniques of structure determination?multiple examples on mode of action of current drugs, ADME-tox properties in drug development, QSAR methods, combinatorial chemistry, biologicals, ribosome, targeting protein-protein interfaces.
出版日期Reference work 2013
關(guān)鍵詞Drug Design; Hit-to-lead optimization; Screening technologies; computer methods and modelling; drug targ
版次1
doihttps://doi.org/10.1007/978-3-642-17907-5
isbn_ebook978-3-642-17907-5
copyrightSpringer-Verlag Berlin Heidelberg 2013
The information of publication is updating

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Reference work 2013ene technology in drug design, omics-technologies computational methods experimental techniques of structure determination?multiple examples on mode of action of current drugs, ADME-tox properties in drug development, QSAR methods, combinatorial chemistry, biologicals, ribosome, targeting protein-protein interfaces.
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發(fā)表于 2025-3-22 03:34:24 | 只看該作者
Reference work 2013ns of 3D structures (these only in electronic form). Makes the spatial aspects of interacting molecules clear to the reader, covers multiple applications and methods in drug design. Structures by mode of action, no therapeutic areas. Of high relevance for academia and industrial research. Focus on g
地板
發(fā)表于 2025-3-22 06:54:31 | 只看該作者
Gerhard KlebeUnique reference work on the subject of drug design.Full colours throughout.Intelligibly written and illustrated containing over 100 computer graphics.Including an index of about 5,000 items
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http://image.papertrans.cn/e/image/283058.jpg
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https://doi.org/10.1007/978-3-642-17907-5Drug Design; Hit-to-lead optimization; Screening technologies; computer methods and modelling; drug targ
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Screening Technologies for Lead Structure Discovery
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tructure determination?multiple examples on mode of action of current drugs, ADME-tox properties in drug development, QSAR methods, combinatorial chemistry, biologicals, ribosome, targeting protein-protein interfaces.978-3-642-17907-5
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