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http://dx.doi.org/10.5012/bkcs.2009.30.6.1313

Discovery of Novel and Potent Cdc25 Phosphatase Inhibitors Based on the Structure-Based De Novo Design  

Park, Hwang-Seo (Department of Bioscience and Biotechnology, Sejong University)
Jung, Suk-Kyeong (Medical Proteomics Research Center, Korea Research Institute of Bioscience and Biotechnology)
Bahn, Young-Jae (Medical Proteomics Research Center, Korea Research Institute of Bioscience and Biotechnology)
Jeong, Dae-Gwin (Medical Proteomics Research Center, Korea Research Institute of Bioscience and Biotechnology)
Ryu, Seong-Eon (Department of Bio-engineering, Hanyang University)
Kim, Seung-Jun (Medical Proteomics Research Center, Korea Research Institute of Bioscience and Biotechnology)
Publication Information
Abstract
Cdc25 phosphatases have been considered as attractive drug targets for anticancer therapy due to the correlation of their overexpression with a wide variety of cancers. We have been able to identify five novel Cdc25 phosphatase inhibitors with micromolar activity by means of a structure-based de novo design method with a known inhibitor scaffold. Because the newly discovered inhibitors are structurally diverse and have desirable physicochemical properties as a drug candidate, they deserve further investigation as anticancer drugs. The differences in binding modes of the identified inhibitors in the active sites of Cdc25A and B are addressed in detail.
Keywords
Cdc25 phosphatase; De novo design; Inhibitor; Anticancer agents;
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