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Nature Medicine
|
September 11, 2019
A single T cell epitope drives the neutralizing anti-drug antibody response to natalizumab in multiple sclerosis patients
Antonino Cassotta, Vincent Mikol, Thomas Bertrand, et al.
Journal of Medicinal Chemistry
|
October 7, 2011
Tricyclic series of heat shock protein 90 (Hsp90) inhibitors part I: discovery of tricyclic imidazo[4,5-c]pyridines as potent inhibitors of the Hsp90 molecular chaperone
François Vallée, Chantal Carrez, Fabienne Pilorge, et al.
ACS Chemical Biology
|
August 23, 2012
In vivo validation of thymidylate kinase (TMK) with a rationally designed, selective antibacterial compound
Thomas A Keating, Joseph V Newman, Nelson B Olivier, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 14, 2005
4,5-Disubstituted cis-pyrrolidinones as inhibitors of type II 17beta-hydroxysteroid dehydrogenase. Part 2. SAR
David Gunn, Christiana Akuche, Jeremy Baryza, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 27, 2004
Omega-carboxypyridyl substituted ureas as Raf kinase inhibitors: SAR of the amide substituent
Uday R Khire, Donald Bankston, James Barbosa, et al.
Journal of Medicinal Chemistry
|
October 10, 2012
Discovery of selective and potent inhibitors of gram-positive bacterial thymidylate kinase (TMK)
Gabriel Martínez-Botella, John N Breen, James E S Duffy, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 1, 2002
Synthesis and pharmacological characterization of a potent, orally active p38 kinase inhibitor
Jacques Dumas, Holia Hatoum-Mokdad, Robert N Sibley, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 19, 2007
SAR of a novel 'Anthranilamide Like' series of VEGFR-2, multi protein kinase inhibitors for the treatment of cancer
Philip Wickens, Harold Kluender, Julie Dixon, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 28) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 28 results.
Nature Medicine
|
September 11, 2019
A single T cell epitope drives the neutralizing anti-drug antibody response to natalizumab in multiple sclerosis patients
Antonino Cassotta, Vincent Mikol, Thomas Bertrand, et al.
Journal of Medicinal Chemistry
|
October 7, 2011
Tricyclic series of heat shock protein 90 (Hsp90) inhibitors part I: discovery of tricyclic imidazo[4,5-c]pyridines as potent inhibitors of the Hsp90 molecular chaperone
François Vallée, Chantal Carrez, Fabienne Pilorge, et al.
ACS Chemical Biology
|
August 23, 2012
In vivo validation of thymidylate kinase (TMK) with a rationally designed, selective antibacterial compound
Thomas A Keating, Joseph V Newman, Nelson B Olivier, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 14, 2005
4,5-Disubstituted cis-pyrrolidinones as inhibitors of type II 17beta-hydroxysteroid dehydrogenase. Part 2. SAR
David Gunn, Christiana Akuche, Jeremy Baryza, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 27, 2004
Omega-carboxypyridyl substituted ureas as Raf kinase inhibitors: SAR of the amide substituent
Uday R Khire, Donald Bankston, James Barbosa, et al.
Journal of Medicinal Chemistry
|
October 10, 2012
Discovery of selective and potent inhibitors of gram-positive bacterial thymidylate kinase (TMK)
Gabriel Martínez-Botella, John N Breen, James E S Duffy, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 1, 2002
Synthesis and pharmacological characterization of a potent, orally active p38 kinase inhibitor
Jacques Dumas, Holia Hatoum-Mokdad, Robert N Sibley, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 19, 2007
SAR of a novel 'Anthranilamide Like' series of VEGFR-2, multi protein kinase inhibitors for the treatment of cancer
Philip Wickens, Harold Kluender, Julie Dixon, et al.
Page
of 3