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Journal of Medicinal Chemistry
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August 23, 2016
Correction to Evolution of a Novel, Orally Bioavailable Series of PI3Kδ Inhibitors from an Inhaled Lead for the Treatment of Respiratory Disease
Augustin Amour, Nick Barton, Anthony W J Cooper, et al.
ACS Medicinal Chemistry Letters
|
July 18, 2020
Design and Development of a Macrocyclic Series Targeting Phosphoinositide 3-Kinase δ
Jonathan A Spencer, Ian R Baldwin, Nick Barton, et al.
The Journal of Biological Chemistry
|
December 15, 2005
Crystal structure of human cytochrome P450 2D6
Paul Rowland, Frank E Blaney, Martin G Smyth, et al.
The Journal of Biological Chemistry
|
December 5, 2024
Pharmacological and structural understanding of the Trypanosoma cruzi proteasome provides key insights for developing site-specific inhibitors
Thomas C Eadsforth, Leah S Torrie, Paul Rowland, et al.
Nature Communications
|
June 13, 2017
Structural and mechanistic basis of differentiated inhibitors of the acute pancreatitis target kynurenine-3-monooxygenase
Jonathan P Hutchinson, Paul Rowland, Mark R D Taylor, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 30, 2009
Second generation of BACE-1 inhibitors part 2: Optimisation of the non-prime side substituent
Nicolas Charrier, Brian Clarke, Emmanuel Demont, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 29, 2010
BACE-1 hydroxyethylamine inhibitors using novel edge-to-face interaction with Arg-296
Brian Clarke, Leanne Cutler, Emmanuel Demont, et al.
ACS Omega
|
September 11, 2018
Isoxazolopyrimidine-Based Inhibitors of
Sreekanth Kokkonda, Farah El Mazouni, Karen L White, et al.
Journal of Medicinal Chemistry
|
February 29, 2020
Targeting the Regulatory Site of ER Aminopeptidase 1 Leads to the Discovery of a Natural Product Modulator of Antigen Presentation
John Liddle, Jonathan P Hutchinson, Semra Kitchen, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 30, 2006
N-(3-Cyano-4,5,6,7-tetrahydro-1-benzothien-2-yl)amides as potent, selective, inhibitors of JNK2 and JNK3
Richard M Angell, Francis L Atkinson, Murray J Brown, et al.
Page
of 5
Search research articles
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Showing results (11-20 of 41) with videos related to
Sort By:
Page
of 5
Journal of Medicinal Chemistry
|
August 23, 2016
Correction to Evolution of a Novel, Orally Bioavailable Series of PI3Kδ Inhibitors from an Inhaled Lead for the Treatment of Respiratory Disease
Augustin Amour, Nick Barton, Anthony W J Cooper, et al.
ACS Medicinal Chemistry Letters
|
July 18, 2020
Design and Development of a Macrocyclic Series Targeting Phosphoinositide 3-Kinase δ
Jonathan A Spencer, Ian R Baldwin, Nick Barton, et al.
The Journal of Biological Chemistry
|
December 15, 2005
Crystal structure of human cytochrome P450 2D6
Paul Rowland, Frank E Blaney, Martin G Smyth, et al.
The Journal of Biological Chemistry
|
December 5, 2024
Pharmacological and structural understanding of the Trypanosoma cruzi proteasome provides key insights for developing site-specific inhibitors
Thomas C Eadsforth, Leah S Torrie, Paul Rowland, et al.
Nature Communications
|
June 13, 2017
Structural and mechanistic basis of differentiated inhibitors of the acute pancreatitis target kynurenine-3-monooxygenase
Jonathan P Hutchinson, Paul Rowland, Mark R D Taylor, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 30, 2009
Second generation of BACE-1 inhibitors part 2: Optimisation of the non-prime side substituent
Nicolas Charrier, Brian Clarke, Emmanuel Demont, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 29, 2010
BACE-1 hydroxyethylamine inhibitors using novel edge-to-face interaction with Arg-296
Brian Clarke, Leanne Cutler, Emmanuel Demont, et al.
ACS Omega
|
September 11, 2018
Isoxazolopyrimidine-Based Inhibitors of
Sreekanth Kokkonda, Farah El Mazouni, Karen L White, et al.
Journal of Medicinal Chemistry
|
February 29, 2020
Targeting the Regulatory Site of ER Aminopeptidase 1 Leads to the Discovery of a Natural Product Modulator of Antigen Presentation
John Liddle, Jonathan P Hutchinson, Semra Kitchen, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 30, 2006
N-(3-Cyano-4,5,6,7-tetrahydro-1-benzothien-2-yl)amides as potent, selective, inhibitors of JNK2 and JNK3
Richard M Angell, Francis L Atkinson, Murray J Brown, et al.
Page
of 5