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Bioorganic & Medicinal Chemistry Letters
|
August 10, 2011
Design and synthesis of novel amide AKT1 inhibitors with selectivity over CDK2
Kate S Ashton, David J St Jean, Steve F Poon, et al.
ACS Chemical Neuroscience
|
August 22, 2017
Structural Determinants of the γ-8 TARP Dependent AMPA Receptor Antagonist
Matthew R Lee, Kevin M Gardinier, Douglas L Gernert, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 4, 2009
Identification of small molecule inhibitors of proline-rich tyrosine kinase 2 (Pyk2) with osteogenic activity in osteoblast cells
John G Allen, Matthew R Lee, Chun-Ya E Han, et al.
Journal of Medicinal Chemistry
|
April 1, 2020
Discovery of Selective Small Molecule Degraders of BRAF-V600E
Xiao-Ran Han, Liqun Chen, Yuanqi Wei, et al.
Microorganisms
|
October 26, 2024
Deep Turbulence as a Novel Main Driver for Multi-Specific Toxic Algal Blooms: The Case of an Anoxic and Heavy Metal-Polluted Submarine Canyon That Harbors Toxic Dinoflagellate Resting Cysts
Camilo Rodríguez-Villegas, Iván Pérez-Santos, Patricio A Díaz, et al.
Antioxidants (Basel, Switzerland)
|
June 27, 2024
The Interactive Effects of the Anti-Sea Lice Pesticide Azamethiphos and Temperature on Oxidative Damage and Antioxidant Responses in the Oyster <i>Ostrea chilensis</i>
Jaime A Montory, Victor M Cubillos, Oscar R Chaparro, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 27, 2011
Identification of triazolopyridazinones as potent p38α inhibitors
Brad Herberich, Claire Jackson, Ryan P Wurz, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 9, 2010
Part 2: Structure-activity relationship (SAR) investigations of fused pyrazoles as potent, selective and orally available inhibitors of p38alpha mitogen-activated protein kinase
Ryan P Wurz, Liping H Pettus, Bradley Henkle, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 4, 2009
Part 1: Structure-Activity Relationship (SAR) investigations of fused pyrazoles as potent, selective and orally available inhibitors of p38alpha mitogen-activated protein kinase
Ryan P Wurz, Liping H Pettus, Shimin Xu, et al.
Journal of Medicinal Chemistry
|
May 12, 2015
Crystal Structures of mPGES-1 Inhibitor Complexes Form a Basis for the Rational Design of Potent Analgesic and Anti-Inflammatory Therapeutics
John Gately Luz, Stephen Antonysamy, Steven L Kuklish, et al.
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of 9
Search research articles
Search
Showing results (41-50 of 81) with videos related to
Sort By:
Page
of 9
Bioorganic & Medicinal Chemistry Letters
|
August 10, 2011
Design and synthesis of novel amide AKT1 inhibitors with selectivity over CDK2
Kate S Ashton, David J St Jean, Steve F Poon, et al.
ACS Chemical Neuroscience
|
August 22, 2017
Structural Determinants of the γ-8 TARP Dependent AMPA Receptor Antagonist
Matthew R Lee, Kevin M Gardinier, Douglas L Gernert, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 4, 2009
Identification of small molecule inhibitors of proline-rich tyrosine kinase 2 (Pyk2) with osteogenic activity in osteoblast cells
John G Allen, Matthew R Lee, Chun-Ya E Han, et al.
Journal of Medicinal Chemistry
|
April 1, 2020
Discovery of Selective Small Molecule Degraders of BRAF-V600E
Xiao-Ran Han, Liqun Chen, Yuanqi Wei, et al.
Microorganisms
|
October 26, 2024
Deep Turbulence as a Novel Main Driver for Multi-Specific Toxic Algal Blooms: The Case of an Anoxic and Heavy Metal-Polluted Submarine Canyon That Harbors Toxic Dinoflagellate Resting Cysts
Camilo Rodríguez-Villegas, Iván Pérez-Santos, Patricio A Díaz, et al.
Antioxidants (Basel, Switzerland)
|
June 27, 2024
The Interactive Effects of the Anti-Sea Lice Pesticide Azamethiphos and Temperature on Oxidative Damage and Antioxidant Responses in the Oyster <i>Ostrea chilensis</i>
Jaime A Montory, Victor M Cubillos, Oscar R Chaparro, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 27, 2011
Identification of triazolopyridazinones as potent p38α inhibitors
Brad Herberich, Claire Jackson, Ryan P Wurz, et al.
Bioorganic & Medicinal Chemistry Letters
|
February 9, 2010
Part 2: Structure-activity relationship (SAR) investigations of fused pyrazoles as potent, selective and orally available inhibitors of p38alpha mitogen-activated protein kinase
Ryan P Wurz, Liping H Pettus, Bradley Henkle, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 4, 2009
Part 1: Structure-Activity Relationship (SAR) investigations of fused pyrazoles as potent, selective and orally available inhibitors of p38alpha mitogen-activated protein kinase
Ryan P Wurz, Liping H Pettus, Shimin Xu, et al.
Journal of Medicinal Chemistry
|
May 12, 2015
Crystal Structures of mPGES-1 Inhibitor Complexes Form a Basis for the Rational Design of Potent Analgesic and Anti-Inflammatory Therapeutics
John Gately Luz, Stephen Antonysamy, Steven L Kuklish, et al.
Page
of 9