Weak affinity chromatography for evaluation of stereoisomers in early drug discovery

In early drug discovery (e.g., in fragment screening), recognition of stereoisomeric structures is valuable and guides medicinal chemists to focus only on useful configurations. In this work, we concurrently screened mixtures of stereoisomers and estimated their affinities to a protein target (throm...

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Main Authors: Duong-Thi, M.-D., Bergstrom, M., Fex, T., Svensson, S., Ohlson, S., Isaksson, R.
其他作者: School of Biological Sciences
格式: Article
語言:English
出版: 2013
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在線閱讀:https://hdl.handle.net/10356/101288
http://hdl.handle.net/10220/16729
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機構: Nanyang Technological University
語言: English