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Titlebook: Modern Methods of Drug Discovery; Alexander Hillisch,Rolf Hilgenfeld Book 2003 Springer Basel AG 2003 Proteomics.biochemistry.bioinformati

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發(fā)表于 2025-3-21 17:01:12 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Modern Methods of Drug Discovery
編輯Alexander Hillisch,Rolf Hilgenfeld
視頻videohttp://file.papertrans.cn/638/637266/637266.mp4
叢書名稱Experientia Supplementum
圖書封面Titlebook: Modern Methods of Drug Discovery;  Alexander Hillisch,Rolf Hilgenfeld Book 2003 Springer Basel AG 2003 Proteomics.biochemistry.bioinformati
描述Research in the pharmaceutical industry today is in many respects quite different from what it used to be only fifteen years ago. There have been dramatic changes in approaches for identifying new chemical entities with a desired biological activity. While chemical modification of existing leads was the most important approach in the 1970s and 1980s, high-throughput screening and structure-based design are now major players among a multitude of methods used in drug discov- ery. Quite often, companies favor one of these relatively new approaches over the other, e.g., screening over rational design, or vice versa, but we believe that an intelligent and concerted use of several or all methods currently available to drug discovery will be more successful in the medium term. What has changed most significantly in the past few years is the time available for identifying new chemical entities. Because of the high costs of drug discovery projects, pressure for maximum success in the shortest possible time is higher than ever. In addition, the multidisciplinary character of the field is much more pronounced today than it used to be. As a consequence, researchers and project managers in the
出版日期Book 2003
關鍵詞Proteomics; biochemistry; bioinformatics; biology; chemistry; drug; drug design; drug development; drug disc
版次1
doihttps://doi.org/10.1007/978-3-0348-7997-2
isbn_softcover978-3-0348-9397-8
isbn_ebook978-3-0348-7997-2Series ISSN 1664-431X Series E-ISSN 2504-3692
issn_series 1664-431X
copyrightSpringer Basel AG 2003
The information of publication is updating

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1664-431X been dramatic changes in approaches for identifying new chemical entities with a desired biological activity. While chemical modification of existing leads was the most important approach in the 1970s and 1980s, high-throughput screening and structure-based design are now major players among a mult
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Book 2003Because of the high costs of drug discovery projects, pressure for maximum success in the shortest possible time is higher than ever. In addition, the multidisciplinary character of the field is much more pronounced today than it used to be. As a consequence, researchers and project managers in the
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Experientia Supplementumhttp://image.papertrans.cn/m/image/637266.jpg
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Antigenic Variation in , to the changing environment in the host and to maintain chronic infection. This chapter discusses antigenic diversity and variation in the malaria parasite and our current understanding of the molecular mechanisms that direct the expression of these proteins.
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