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Huilin Zhao

Amgen

17

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907

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Structural basis for the potent and selective inhibition of casein kinase 1 epsilon.

2012 Journal of Medicinal Chemistry
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Structure-Based Design of Potent and Selective CK1γ Inhibitors.

2012 ACS Medicinal Chemistry Letters
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Structural basis for the interaction between casein kinase 1 delta and a potent and selective inhibitor.

2012 Journal of Medicinal Chemistry
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Structure-Based Design of Potent and Selective CK1 gamma Inhibitors.

2012 ACS Medicinal Chemistry Letters
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Discovery of a potent, selective, and orally bioavailable pyridinyl-pyrimidine phthalazine aurora kinase inhibitor.

2010 Journal of Medicinal Chemistry
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Identification of small molecule inhibitors of proline-rich tyrosine kinase 2 (Pyk2) with osteogenic activity in osteoblast cells

2009 Bioorganic & Medicinal Chemistry Letters
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Structure-Based Design of Novel 2-Amino-6-phenyl-pyrimido[5′,4′:5,6]pyrimido[1,2-a]benzimidazol-5(6H)-ones as Potent and Orally Active Inhibitors of Lymphocyte Specific Kinase (Lck): Synthesis, SAR, and In Vivo Anti-Inflammatory Activity

2008 Journal of Medicinal Chemistry
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Structure-Guided Design of Aminopyrimidine Amides as Potent, Selective Inhibitors of Lymphocyte Specific Kinase: Synthesis, Structure–Activity Relationships, and Inhibition of in Vivo T Cell Activation

2008 Journal of Medicinal Chemistry
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Design, Synthesis, and Evaluation of Orally Active Benzimidazoles and Benzoxazoles as Vascular Endothelial Growth Factor-2 Receptor Tyrosine Kinase Inhibitors.

2007 Journal of Medicinal Chemistry
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Alkynylpyrimidine amide derivatives as potent, selective, and orally active inhibitors of Tie-2 kinase.

2007 Journal of Medicinal Chemistry
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