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ACS Medicinal Chemistry Letters
|
December 21, 2016
Buried Hydrogen Bond Interactions Contribute to the High Potency of Complement Factor D Inhibitors
Chao-Yie Yang, James G Phillips, Jeanne A Stuckey, et al.
Journal of Medicinal Chemistry
|
November 18, 2008
Design, synthesis, and evaluation of tricyclic, conformationally constrained small-molecule mimetics of second mitochondria-derived activator of caspases
Bin Zhang, Zaneta Nikolovska-Coleska, Yan Zhang, et al.
The Journal of Biological Chemistry
|
September 18, 2007
Reduced pepsin A processing of sonic hedgehog in parietal cells precedes gastric atrophy and transformation
Yana Zavros, Meghna Waghray, Arthur Tessier, et al.
Journal of Medicinal Chemistry
|
March 2, 2013
A potent and highly efficacious Bcl-2/Bcl-xL inhibitor
Angelo Aguilar, Haibin Zhou, Jianfang Chen, et al.
Plos One
|
March 23, 2013
Gli1 deletion prevents Helicobacter-induced gastric metaplasia and expansion of myeloid cell subsets
Mohamad El-Zaatari, John Y Kao, Art Tessier, et al.
Accounts of Chemical Research
|
October 22, 2008
Design of small-molecule peptidic and nonpeptidic Smac mimetics
Haiying Sun, Zaneta Nikolovska-Coleska, Chao-Yie Yang, et al.
Journal of Medicinal Chemistry
|
June 17, 2015
Structure-Based Design of γ-Carboline Analogues as Potent and Specific BET Bromodomain Inhibitors
Xu Ran, Yujun Zhao, Liu Liu, et al.
Journal of Medicinal Chemistry
|
October 4, 2012
Structure-based discovery of BM-957 as a potent small-molecule inhibitor of Bcl-2 and Bcl-xL capable of achieving complete tumor regression
Jianfang Chen, Haibin Zhou, Angelo Aguilar, et al.
Journal of Medicinal Chemistry
|
July 5, 2026
Discovery of SD-2301 as a Highly Potent and Selective PROTAC STAT3 Degrader Capable of Achieving Complete Tumor Regression with Single Administration
Ranjan Kumar Acharyya, Longchuan Bai, Haibin Zhou, et al.
Journal of Medicinal Chemistry
|
July 4, 2012
Structure-based design of potent Bcl-2/Bcl-xL inhibitors with strong in vivo antitumor activity
Haibin Zhou, Angelo Aguilar, Jianfang Chen, et al.
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Search research articles
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Showing results (21-30 of 67) with videos related to
Sort By:
Page
of 7
ACS Medicinal Chemistry Letters
|
December 21, 2016
Buried Hydrogen Bond Interactions Contribute to the High Potency of Complement Factor D Inhibitors
Chao-Yie Yang, James G Phillips, Jeanne A Stuckey, et al.
Journal of Medicinal Chemistry
|
November 18, 2008
Design, synthesis, and evaluation of tricyclic, conformationally constrained small-molecule mimetics of second mitochondria-derived activator of caspases
Bin Zhang, Zaneta Nikolovska-Coleska, Yan Zhang, et al.
The Journal of Biological Chemistry
|
September 18, 2007
Reduced pepsin A processing of sonic hedgehog in parietal cells precedes gastric atrophy and transformation
Yana Zavros, Meghna Waghray, Arthur Tessier, et al.
Journal of Medicinal Chemistry
|
March 2, 2013
A potent and highly efficacious Bcl-2/Bcl-xL inhibitor
Angelo Aguilar, Haibin Zhou, Jianfang Chen, et al.
Plos One
|
March 23, 2013
Gli1 deletion prevents Helicobacter-induced gastric metaplasia and expansion of myeloid cell subsets
Mohamad El-Zaatari, John Y Kao, Art Tessier, et al.
Accounts of Chemical Research
|
October 22, 2008
Design of small-molecule peptidic and nonpeptidic Smac mimetics
Haiying Sun, Zaneta Nikolovska-Coleska, Chao-Yie Yang, et al.
Journal of Medicinal Chemistry
|
June 17, 2015
Structure-Based Design of γ-Carboline Analogues as Potent and Specific BET Bromodomain Inhibitors
Xu Ran, Yujun Zhao, Liu Liu, et al.
Journal of Medicinal Chemistry
|
October 4, 2012
Structure-based discovery of BM-957 as a potent small-molecule inhibitor of Bcl-2 and Bcl-xL capable of achieving complete tumor regression
Jianfang Chen, Haibin Zhou, Angelo Aguilar, et al.
Journal of Medicinal Chemistry
|
July 5, 2026
Discovery of SD-2301 as a Highly Potent and Selective PROTAC STAT3 Degrader Capable of Achieving Complete Tumor Regression with Single Administration
Ranjan Kumar Acharyya, Longchuan Bai, Haibin Zhou, et al.
Journal of Medicinal Chemistry
|
July 4, 2012
Structure-based design of potent Bcl-2/Bcl-xL inhibitors with strong in vivo antitumor activity
Haibin Zhou, Angelo Aguilar, Jianfang Chen, et al.
Page
of 7