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Bioorganic & Medicinal Chemistry Letters
|
November 4, 2011
CCR2 receptor antagonists: optimization of biaryl sulfonamides to increase activity in whole blood
Gren Z Wang, Pamela A Haile, Tom Daniel, et al.
Journal of Medicinal Chemistry
|
January 29, 2019
Identification and Optimization of Novel Small c-Abl Kinase Activators Using Fragment and HTS Methodologies
Graham L Simpson, Sophie M Bertrand, Jennifer A Borthwick, et al.
Assay and Drug Development Technologies
|
June 19, 2013
Development of a high-throughput screen to detect inhibitors of TRPS1 sumoylation
Martin Brandt, Lawrence M Szewczuk, Hong Zhang, et al.
Journal of Medicinal Chemistry
|
July 26, 2012
Discovery of 7-methyl-5-(1-{[3-(trifluoromethyl)phenyl]acetyl}-2,3-dihydro-1H-indol-5-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine (GSK2606414), a potent and selective first-in-class inhibitor of protein kinase R (PKR)-like endoplasmic reticulum kinase (PERK)
Jeffrey M Axten, Jesús R Medina, Yanhong Feng, et al.
Chemistry & Biology
|
February 23, 2011
Discovery and characterization of a cell-permeable, small-molecule c-Abl kinase activator that binds to the myristoyl binding site
Jingsong Yang, Nino Campobasso, Mangatt P Biju, et al.
Nature Chemical Biology
|
March 26, 2013
Selective class IIa histone deacetylase inhibition via a nonchelating zinc-binding group
Mercedes Lobera, Kevin P Madauss, Denise T Pohlhaus, et al.
Biotechnology and Bioengineering
|
April 8, 2020
Highland games: A benchmarking exercise in predicting biophysical and drug properties of monoclonal antibodies from amino acid sequences
Jonathan Coffman, Bruno Marques, Raquel Orozco, et al.
Cancer Cell
|
December 12, 2018
Targeting PKCδ as a Therapeutic Strategy against Heterogeneous Mechanisms of EGFR Inhibitor Resistance in EGFR-Mutant Lung Cancer
Pei-Chih Lee, Yueh-Fu Fang, Hirohito Yamaguchi, et al.
Page
of 15
Search research articles
Search
Showing results (141-150 of 148) with videos related to
Sort By:
Page
of 15
You have reached the last page of results.
This site can display upto 148 results.
Bioorganic & Medicinal Chemistry Letters
|
November 4, 2011
CCR2 receptor antagonists: optimization of biaryl sulfonamides to increase activity in whole blood
Gren Z Wang, Pamela A Haile, Tom Daniel, et al.
Journal of Medicinal Chemistry
|
January 29, 2019
Identification and Optimization of Novel Small c-Abl Kinase Activators Using Fragment and HTS Methodologies
Graham L Simpson, Sophie M Bertrand, Jennifer A Borthwick, et al.
Assay and Drug Development Technologies
|
June 19, 2013
Development of a high-throughput screen to detect inhibitors of TRPS1 sumoylation
Martin Brandt, Lawrence M Szewczuk, Hong Zhang, et al.
Journal of Medicinal Chemistry
|
July 26, 2012
Discovery of 7-methyl-5-(1-{[3-(trifluoromethyl)phenyl]acetyl}-2,3-dihydro-1H-indol-5-yl)-7H-pyrrolo[2,3-d]pyrimidin-4-amine (GSK2606414), a potent and selective first-in-class inhibitor of protein kinase R (PKR)-like endoplasmic reticulum kinase (PERK)
Jeffrey M Axten, Jesús R Medina, Yanhong Feng, et al.
Chemistry & Biology
|
February 23, 2011
Discovery and characterization of a cell-permeable, small-molecule c-Abl kinase activator that binds to the myristoyl binding site
Jingsong Yang, Nino Campobasso, Mangatt P Biju, et al.
Nature Chemical Biology
|
March 26, 2013
Selective class IIa histone deacetylase inhibition via a nonchelating zinc-binding group
Mercedes Lobera, Kevin P Madauss, Denise T Pohlhaus, et al.
Biotechnology and Bioengineering
|
April 8, 2020
Highland games: A benchmarking exercise in predicting biophysical and drug properties of monoclonal antibodies from amino acid sequences
Jonathan Coffman, Bruno Marques, Raquel Orozco, et al.
Cancer Cell
|
December 12, 2018
Targeting PKCδ as a Therapeutic Strategy against Heterogeneous Mechanisms of EGFR Inhibitor Resistance in EGFR-Mutant Lung Cancer
Pei-Chih Lee, Yueh-Fu Fang, Hirohito Yamaguchi, et al.
Page
of 15