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New Quinoxaline Derivatives as Dual Pim-1/2 Kinase Inhibitors: Design, Synthesis and Biological Evaluation.

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第一作者: Bruno,Oyallon
第一单位: EA GICC-ERL 7001 CNRS, Team IMT, University of Tours, F-37200 Tours, France.
作者单位: EA GICC-ERL 7001 CNRS, Team IMT, University of Tours, F-37200 Tours, France. [1] CNRS ERL7001 LNOx-EA GICC, University of Tours, F-37000 Tours, France. [2] Department of Medicinal Chemistry, IICIMED-EA1155, IRS2, University of Nantes, F-44200 Nantes, France. [3] Integrative Biology of Marine Models Laboratory (LBI2M), Sorbonne University, CNRS, UMR8227, F-29680 Roscoff, France.;Kinase Inhibitor Specialized Screening facility (KISSf), Sorbonne University, CNRS, FR2424, F-29680 Roscoff, France. [4] Integrative Biology of Marine Models Laboratory (LBI2M), Sorbonne University, CNRS, UMR8227, F-29680 Roscoff, France.;Kinase Inhibitor Specialized Screening facility (KISSf), Sorbonne University, CNRS, FR2424, F-29680 Roscoff, France.;Centre of Excellence for Pharmaceutical Sciences, North-West University, Private Bag X6001, Potchefstroom 2520, South Africa. [5] EA GICC-ERL 7001 CNRS, Team PATCH, University of Tours, F-37200 Tours, France. [6] EA GICC-ERL 7001 CNRS, Team PATCH, University of Tours, F-37200 Tours, France.;N2C, University of Tours, INSERM, UMR 1069, F-37032 Tours, France. [7] UMR-S 1172-JPArc, University of Lille, INSERM, CHU Lille, F-59000 Lille, France. [8] ARNA Laboratory, University of Bordeaux, INSERM U12132-UMR CNRS 5320, F-33076 Bordeaux, France. [9] ISM, University of Bordeaux, CNRS, UMR 5255, F-33405 Talence, France. [10]
DOI 10.3390/molecules26040867
PMID 33562106
发布时间 2021-12-04
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Molecules (Basel, Switzerland)

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