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Journal of the American Chemical Society
|
November 15, 2007
Design, synthesis, and characterization of a potent, nonpeptide, cell-permeable, bivalent Smac mimetic that concurrently targets both the BIR2 and BIR3 domains in XIAP
Haiying Sun, Zaneta Nikolovska-Coleska, Jianfeng Lu, et al.
Scientific Reports
|
February 5, 2022
Genetic studies of fall armyworm indicate a new introduction into Africa and identify limits to its migratory behavior
Rodney N Nagoshi, Georg Goergen, Djima Koffi, et al.
Journal of the American Chemical Society
|
February 7, 2013
Ordering a dynamic protein via a small-molecule stabilizer
Ningkun Wang, Chinmay Y Majmudar, William C Pomerantz, et al.
Journal of Medicinal Chemistry
|
January 2, 2025
Discovery of High-Affinity SMARCA2/4 Bromodomain Ligands and Development of Potent and Exceptionally Selective SMARCA2 PROTAC Degraders
Lingying Leng, Wenbin Tu, Lin Yang, et al.
Journal of Medicinal Chemistry
|
May 3, 2017
Structure-Based Discovery of 4-(6-Methoxy-2-methyl-4-(quinolin-4-yl)-9H-pyrimido[4,5-b]indol-7-yl)-3,5-dimethylisoxazole (CD161) as a Potent and Orally Bioavailable BET Bromodomain Inhibitor
Yujun Zhao, Longchuan Bai, Liu Liu, et al.
Journal of Medicinal Chemistry
|
September 23, 2024
Discovery of AK-1690: A Potent and Highly Selective STAT6 PROTAC Degrader
Atsunori Kaneshige, Yiqing Yang, Longchuan Bai, et al.
BMC Genomics
|
February 7, 2025
Genomic patterns of strain-specific genetic structure, linkage, and selection across fall armyworm populations
Ashley E Tessnow, Rodney N Nagoshi, Robert L Meagher, et al.
Nature Chemical Biology
|
February 2, 2023
A selective small-molecule STAT5 PROTAC degrader capable of achieving tumor regression in vivo
Atsunori Kaneshige, Longchuan Bai, Mi Wang, et al.
Journal of Medicinal Chemistry
|
November 7, 2024
Discovery of SD-436: A Potent, Highly Selective and Efficacious STAT3 PROTAC Degrader Capable of Achieving Complete and Long-Lasting Tumor Regression
Renqi Xu, Haibin Zhou, Longchuan Bai, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 30, 2008
Discovery of amido-benzisoxazoles as potent c-Kit inhibitors
Roxanne K Kunz, Shannon Rumfelt, Ning Chen, et al.
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Search research articles
Search
Showing results (121-130 of 143) with videos related to
Sort By:
Page
of 15
Journal of the American Chemical Society
|
November 15, 2007
Design, synthesis, and characterization of a potent, nonpeptide, cell-permeable, bivalent Smac mimetic that concurrently targets both the BIR2 and BIR3 domains in XIAP
Haiying Sun, Zaneta Nikolovska-Coleska, Jianfeng Lu, et al.
Scientific Reports
|
February 5, 2022
Genetic studies of fall armyworm indicate a new introduction into Africa and identify limits to its migratory behavior
Rodney N Nagoshi, Georg Goergen, Djima Koffi, et al.
Journal of the American Chemical Society
|
February 7, 2013
Ordering a dynamic protein via a small-molecule stabilizer
Ningkun Wang, Chinmay Y Majmudar, William C Pomerantz, et al.
Journal of Medicinal Chemistry
|
January 2, 2025
Discovery of High-Affinity SMARCA2/4 Bromodomain Ligands and Development of Potent and Exceptionally Selective SMARCA2 PROTAC Degraders
Lingying Leng, Wenbin Tu, Lin Yang, et al.
Journal of Medicinal Chemistry
|
May 3, 2017
Structure-Based Discovery of 4-(6-Methoxy-2-methyl-4-(quinolin-4-yl)-9H-pyrimido[4,5-b]indol-7-yl)-3,5-dimethylisoxazole (CD161) as a Potent and Orally Bioavailable BET Bromodomain Inhibitor
Yujun Zhao, Longchuan Bai, Liu Liu, et al.
Journal of Medicinal Chemistry
|
September 23, 2024
Discovery of AK-1690: A Potent and Highly Selective STAT6 PROTAC Degrader
Atsunori Kaneshige, Yiqing Yang, Longchuan Bai, et al.
BMC Genomics
|
February 7, 2025
Genomic patterns of strain-specific genetic structure, linkage, and selection across fall armyworm populations
Ashley E Tessnow, Rodney N Nagoshi, Robert L Meagher, et al.
Nature Chemical Biology
|
February 2, 2023
A selective small-molecule STAT5 PROTAC degrader capable of achieving tumor regression in vivo
Atsunori Kaneshige, Longchuan Bai, Mi Wang, et al.
Journal of Medicinal Chemistry
|
November 7, 2024
Discovery of SD-436: A Potent, Highly Selective and Efficacious STAT3 PROTAC Degrader Capable of Achieving Complete and Long-Lasting Tumor Regression
Renqi Xu, Haibin Zhou, Longchuan Bai, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 30, 2008
Discovery of amido-benzisoxazoles as potent c-Kit inhibitors
Roxanne K Kunz, Shannon Rumfelt, Ning Chen, et al.
Page
of 15