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Drug Discovery Today
|
September 26, 2006
Chemogenomics: structuring the drug discovery process to gene families
C John Harris, Adrian P Stevens
Combinatorial Chemistry & High Throughput Screening
|
August 5, 2008
How large does a compound screening collection need to be?
Michael J Lipkin, Adrian P Stevens, David J Livingstone, et al.
Current Medicinal Chemistry
|
June 22, 2006
Bringing kinases into focus: efficient drug design through the use of chemogenomic toolkits
Veronique Birault, C John Harris, Joelle Le, et al.
Current Pharmaceutical Design
|
August 17, 2013
Strategies for small molecule library design
David W Sheppard, Michael J Lipkin, C John Harris, et al.
Combinatorial Chemistry & High Throughput Screening
|
April 28, 2011
The design and application of target-focused compound libraries
C John Harris, Richard D Hill, David W Sheppard, et al.
Bioorganic & Medicinal Chemistry
|
November 3, 2015
Aminopyrazolo[1,5-a]pyrimidines as potential inhibitors of Mycobacterium tuberculosis: Structure activity relationships and ADME characterization
Candice Soares de Melo, Soares de Melo Candice, Tzu-Shean Feng, et al.
Journal of Medicinal Chemistry
|
July 4, 2012
Mitogen-activated protein kinase-activated protein kinase 2 (MAPKAP-K2) as an antiinflammatory target: discovery and in vivo activity of selective pyrazolo[1,5-a]pyrimidine inhibitors using a focused library and structure-based optimization approach
Tomomi Kosugi, Dale R Mitchell, Aiko Fujino, et al.
Journal of Medicinal Chemistry
|
May 21, 2020
Discovery of Highly Selective Inhibitors of Calmodulin-Dependent Kinases That Restore Insulin Sensitivity in the Diet-Induced Obesity <i>in Vivo</i> Mouse Model
Christophe Fromont, Alessio Atzori, Divneet Kaur, et al.
Journal of Medicinal Chemistry
|
November 18, 2017
Novel Antitubercular 6-Dialkylaminopyrimidine Carboxamides from Phenotypic Whole-Cell High Throughput Screening of a SoftFocus Library: Structure-Activity Relationship and Target Identification Studies
Colin R Wilson, Richard K Gessner, Atica Moosa, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Drug Discovery Today
|
September 26, 2006
Chemogenomics: structuring the drug discovery process to gene families
C John Harris, Adrian P Stevens
Combinatorial Chemistry & High Throughput Screening
|
August 5, 2008
How large does a compound screening collection need to be?
Michael J Lipkin, Adrian P Stevens, David J Livingstone, et al.
Current Medicinal Chemistry
|
June 22, 2006
Bringing kinases into focus: efficient drug design through the use of chemogenomic toolkits
Veronique Birault, C John Harris, Joelle Le, et al.
Current Pharmaceutical Design
|
August 17, 2013
Strategies for small molecule library design
David W Sheppard, Michael J Lipkin, C John Harris, et al.
Combinatorial Chemistry & High Throughput Screening
|
April 28, 2011
The design and application of target-focused compound libraries
C John Harris, Richard D Hill, David W Sheppard, et al.
Bioorganic & Medicinal Chemistry
|
November 3, 2015
Aminopyrazolo[1,5-a]pyrimidines as potential inhibitors of Mycobacterium tuberculosis: Structure activity relationships and ADME characterization
Candice Soares de Melo, Soares de Melo Candice, Tzu-Shean Feng, et al.
Journal of Medicinal Chemistry
|
July 4, 2012
Mitogen-activated protein kinase-activated protein kinase 2 (MAPKAP-K2) as an antiinflammatory target: discovery and in vivo activity of selective pyrazolo[1,5-a]pyrimidine inhibitors using a focused library and structure-based optimization approach
Tomomi Kosugi, Dale R Mitchell, Aiko Fujino, et al.
Journal of Medicinal Chemistry
|
May 21, 2020
Discovery of Highly Selective Inhibitors of Calmodulin-Dependent Kinases That Restore Insulin Sensitivity in the Diet-Induced Obesity <i>in Vivo</i> Mouse Model
Christophe Fromont, Alessio Atzori, Divneet Kaur, et al.
Journal of Medicinal Chemistry
|
November 18, 2017
Novel Antitubercular 6-Dialkylaminopyrimidine Carboxamides from Phenotypic Whole-Cell High Throughput Screening of a SoftFocus Library: Structure-Activity Relationship and Target Identification Studies
Colin R Wilson, Richard K Gessner, Atica Moosa, et al.
Page
of 1