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Cancer Cell
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November 13, 2019
A Potent and Selective Small-Molecule Degrader of STAT3 Achieves Complete Tumor Regression In Vivo
Longchuan Bai, Haibin Zhou, Renqi Xu, et al.
Scientific Reports
|
January 13, 2021
Targeted disruption of pi-pi stacking in Malaysian banana lectin reduces mitogenicity while preserving antiviral activity
Evelyn M Covés-Datson, Steven R King, Maureen Legendre, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 17, 2008
Discovery of a potent and selective c-Kit inhibitor for the treatment of inflammatory diseases
Ning Chen, Roland W Bürli, Susana Neira, et al.
Journal of Medicinal Chemistry
|
November 21, 2019
Structure-Based Discovery of SD-36 as a Potent, Selective, and Efficacious PROTAC Degrader of STAT3 Protein
Haibin Zhou, Longchuan Bai, Renqi Xu, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society
|
December 28, 2020
Lipid-based vaccine nanoparticles for induction of humoral immune responses against HIV-1 and SARS-CoV-2
Kyung Soo Park, Joseph D Bazzill, Sejin Son, et al.
Journal of Medicinal Chemistry
|
January 2, 2025
Discovery of SMD-3236: A Potent, Highly Selective and Efficacious SMARCA2 Degrader for the Treatment of SMARC4-Deficient Human Cancers
Lin Yang, Wenbin Tu, Lingying Leng, et al.
Journal of Medicinal Chemistry
|
January 24, 2020
Discovery and Characterization of 2,5-Substituted Benzoic Acid Dual Inhibitors of the Anti-apoptotic Mcl-1 and Bfl-1 Proteins
Karson J Kump, Lei Miao, Ahmed S A Mady, et al.
Journal of Medicinal Chemistry
|
July 18, 2018
Structure-Based Discovery of CF53 as a Potent and Orally Bioavailable Bromodomain and Extra-Terminal (BET) Bromodomain Inhibitor
Yujun Zhao, Bing Zhou, Longchuan Bai, et al.
Journal of Medicinal Chemistry
|
May 2, 2008
Discovery of aryl aminoquinazoline pyridones as potent, selective, and orally efficacious inhibitors of receptor tyrosine kinase c-Kit
Essa Hu, Andrew Tasker, Ryan D White, et al.
ACS Chemical Biology
|
November 1, 2016
Molecular Mechanism for Isoform-Selective Inhibition of Acyl Protein Thioesterases 1 and 2 (APT1 and APT2)
Sang Joon Won, Dahvid Davda, Kristin J Labby, et al.
Page
of 15
Search research articles
Search
Showing results (131-140 of 143) with videos related to
Sort By:
Page
of 15
Cancer Cell
|
November 13, 2019
A Potent and Selective Small-Molecule Degrader of STAT3 Achieves Complete Tumor Regression In Vivo
Longchuan Bai, Haibin Zhou, Renqi Xu, et al.
Scientific Reports
|
January 13, 2021
Targeted disruption of pi-pi stacking in Malaysian banana lectin reduces mitogenicity while preserving antiviral activity
Evelyn M Covés-Datson, Steven R King, Maureen Legendre, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 17, 2008
Discovery of a potent and selective c-Kit inhibitor for the treatment of inflammatory diseases
Ning Chen, Roland W Bürli, Susana Neira, et al.
Journal of Medicinal Chemistry
|
November 21, 2019
Structure-Based Discovery of SD-36 as a Potent, Selective, and Efficacious PROTAC Degrader of STAT3 Protein
Haibin Zhou, Longchuan Bai, Renqi Xu, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society
|
December 28, 2020
Lipid-based vaccine nanoparticles for induction of humoral immune responses against HIV-1 and SARS-CoV-2
Kyung Soo Park, Joseph D Bazzill, Sejin Son, et al.
Journal of Medicinal Chemistry
|
January 2, 2025
Discovery of SMD-3236: A Potent, Highly Selective and Efficacious SMARCA2 Degrader for the Treatment of SMARC4-Deficient Human Cancers
Lin Yang, Wenbin Tu, Lingying Leng, et al.
Journal of Medicinal Chemistry
|
January 24, 2020
Discovery and Characterization of 2,5-Substituted Benzoic Acid Dual Inhibitors of the Anti-apoptotic Mcl-1 and Bfl-1 Proteins
Karson J Kump, Lei Miao, Ahmed S A Mady, et al.
Journal of Medicinal Chemistry
|
July 18, 2018
Structure-Based Discovery of CF53 as a Potent and Orally Bioavailable Bromodomain and Extra-Terminal (BET) Bromodomain Inhibitor
Yujun Zhao, Bing Zhou, Longchuan Bai, et al.
Journal of Medicinal Chemistry
|
May 2, 2008
Discovery of aryl aminoquinazoline pyridones as potent, selective, and orally efficacious inhibitors of receptor tyrosine kinase c-Kit
Essa Hu, Andrew Tasker, Ryan D White, et al.
ACS Chemical Biology
|
November 1, 2016
Molecular Mechanism for Isoform-Selective Inhibition of Acyl Protein Thioesterases 1 and 2 (APT1 and APT2)
Sang Joon Won, Dahvid Davda, Kristin J Labby, et al.
Page
of 15