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ACS Chemical Biology
|
December 22, 2009
In vivo structure-activity relationship study of dorsomorphin analogues identifies selective VEGF and BMP inhibitors
Jijun Hao, Joshua N Ho, Jana A Lewis, et al.
Chemical Research in Toxicology
|
June 1, 2018
Cytochromes P450 1A2 and 3A4 Catalyze the Metabolic Activation of Sunitinib
Gracia M Amaya, Rebecca Durandis, David S Bourgeois, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 20, 2014
Approach for targeting Ras with small molecules that activate SOS-mediated nucleotide exchange
Michael C Burns, Qi Sun, R Nathan Daniels, et al.
Journal of Medicinal Chemistry
|
December 19, 2012
Discovery of potent myeloid cell leukemia 1 (Mcl-1) inhibitors using fragment-based methods and structure-based design
Anders Friberg, Dominico Vigil, Bin Zhao, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 28, 2014
Novel GlyT1 inhibitor chemotypes by scaffold hopping. Part 2: development of a [3.3.0]-based series and other piperidine bioisosteres
Douglas J Sheffler, Michael T Nedelcovych, Richard Williams, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 23, 2008
Synthesis and SAR of analogues of the M1 allosteric agonist TBPB. Part I: Exploration of alternative benzyl and privileged structure moieties
Thomas M Bridges, Ashley E Brady, J Phillip Kennedy, et al.
Journal of Medicinal Chemistry
|
June 2, 2018
Discovery of Aminopiperidine Indoles That Activate the Guanine Nucleotide Exchange Factor SOS1 and Modulate RAS Signaling
Jason R Abbott, Timothy R Hodges, R Nathan Daniels, et al.
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Search research articles
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Showing results (11-20 of 17) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 17 results.
ACS Chemical Biology
|
December 22, 2009
In vivo structure-activity relationship study of dorsomorphin analogues identifies selective VEGF and BMP inhibitors
Jijun Hao, Joshua N Ho, Jana A Lewis, et al.
Chemical Research in Toxicology
|
June 1, 2018
Cytochromes P450 1A2 and 3A4 Catalyze the Metabolic Activation of Sunitinib
Gracia M Amaya, Rebecca Durandis, David S Bourgeois, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 20, 2014
Approach for targeting Ras with small molecules that activate SOS-mediated nucleotide exchange
Michael C Burns, Qi Sun, R Nathan Daniels, et al.
Journal of Medicinal Chemistry
|
December 19, 2012
Discovery of potent myeloid cell leukemia 1 (Mcl-1) inhibitors using fragment-based methods and structure-based design
Anders Friberg, Dominico Vigil, Bin Zhao, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 28, 2014
Novel GlyT1 inhibitor chemotypes by scaffold hopping. Part 2: development of a [3.3.0]-based series and other piperidine bioisosteres
Douglas J Sheffler, Michael T Nedelcovych, Richard Williams, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 23, 2008
Synthesis and SAR of analogues of the M1 allosteric agonist TBPB. Part I: Exploration of alternative benzyl and privileged structure moieties
Thomas M Bridges, Ashley E Brady, J Phillip Kennedy, et al.
Journal of Medicinal Chemistry
|
June 2, 2018
Discovery of Aminopiperidine Indoles That Activate the Guanine Nucleotide Exchange Factor SOS1 and Modulate RAS Signaling
Jason R Abbott, Timothy R Hodges, R Nathan Daniels, et al.
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of 2