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Journal of Medicinal Chemistry
|
May 19, 2012
A selective, orally bioavailable 1,2,4-triazolo[1,5-a]pyridine-based inhibitor of Janus kinase 2 for use in anticancer therapy: discovery of CEP-33779
Benjamin J Dugan, Diane E Gingrich, Eugen F Mesaros, et al.
Journal of Medicinal Chemistry
|
December 7, 2011
Strategies to mitigate the bioactivation of 2-anilino-7-aryl-pyrrolo[2,1-f][1,2,4]triazines: identification of orally bioavailable, efficacious ALK inhibitors
Eugen F Mesaros, Tho V Thieu, Gregory J Wells, et al.
Journal of Medicinal Chemistry
|
August 17, 2016
Discovery of Clinical Candidate CEP-37440, a Selective Inhibitor of Focal Adhesion Kinase (FAK) and Anaplastic Lymphoma Kinase (ALK)
Gregory R Ott, Mangeng Cheng, Keith S Learn, et al.
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of 4
Search research articles
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Showing results (31-40 of 33) with videos related to
Sort By:
Page
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You have reached the last page of results.
This site can display upto 33 results.
Journal of Medicinal Chemistry
|
May 19, 2012
A selective, orally bioavailable 1,2,4-triazolo[1,5-a]pyridine-based inhibitor of Janus kinase 2 for use in anticancer therapy: discovery of CEP-33779
Benjamin J Dugan, Diane E Gingrich, Eugen F Mesaros, et al.
Journal of Medicinal Chemistry
|
December 7, 2011
Strategies to mitigate the bioactivation of 2-anilino-7-aryl-pyrrolo[2,1-f][1,2,4]triazines: identification of orally bioavailable, efficacious ALK inhibitors
Eugen F Mesaros, Tho V Thieu, Gregory J Wells, et al.
Journal of Medicinal Chemistry
|
August 17, 2016
Discovery of Clinical Candidate CEP-37440, a Selective Inhibitor of Focal Adhesion Kinase (FAK) and Anaplastic Lymphoma Kinase (ALK)
Gregory R Ott, Mangeng Cheng, Keith S Learn, et al.
Page
of 4