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The Journal of Biological Chemistry
|
May 2, 2013
Atypical antigen recognition mode of a shark immunoglobulin new antigen receptor (IgNAR) variable domain characterized by humanization and structural analysis
Oleg V Kovalenko, Andrea Olland, Nicole Piché-Nicholas, et al.
Bioorganic & Medicinal Chemistry
|
January 5, 2010
Di-substituted pyridinyl aminohydantoins as potent and highly selective human beta-secretase (BACE1) inhibitors
Michael S Malamas, Keith Barnes, Matthew Johnson, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 26, 2009
4-(3-Aryloxyaryl)quinoline sulfones are potent liver X receptor agonists
Ronald C Bernotas, Robert R Singhaus, David H Kaufman, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 6, 2010
Pyridinyl aminohydantoins as small molecule BACE1 inhibitors
Ping Zhou, Yanfang Li, Yi Fan, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 1, 2011
Discovery of a stable macrocyclic o-aminobenzamide Hsp90 inhibitor which significantly decreases tumor volume in a mouse xenograft model
Christoph W Zapf, Jonathan D Bloom, Zhong Li, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 13, 2010
Novel pyrrolyl 2-aminopyridines as potent and selective human beta-secretase (BACE1) inhibitors
Michael S Malamas, Keith Barnes, Yu Hui, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 23, 2019
Inhibition of 3-phosphoglycerate dehydrogenase (PHGDH) by indole amides abrogates de novo serine synthesis in cancer cells
Edouard Mullarky, Jiayi Xu, Anita D Robin, et al.
RSC Medicinal Chemistry
|
April 18, 2022
The identification of highly efficacious functionalised tetrahydrocyclopenta[<i>c</i>]pyrroles as inhibitors of HBV viral replication through modulation of HBV capsid assembly
Andrew G Cole, Steven G Kultgen, Nagraj Mani, et al.
Journal of Medicinal Chemistry
|
August 5, 2005
Synthesis and structure-activity relationship of novel 6-aryl-1,4-dihydrobenzo[d][1,3]oxazine-2-thiones as progesterone receptor modulators leading to the potent and selective nonsteroidal progesterone receptor agonist tanaproget
Andrew Fensome, Reinhold Bender, Rajiv Chopra, et al.
Journal of Medicinal Chemistry
|
September 4, 2024
Rational Design, Synthesis, and Structure-Activity Relationship of a Novel Isoquinolinone-Based Series of HBV Capsid Assembly Modulators Leading to the Identification of Clinical Candidate AB-836
Andrew G Cole, Steven G Kultgen, Nagraj Mani, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
The Journal of Biological Chemistry
|
May 2, 2013
Atypical antigen recognition mode of a shark immunoglobulin new antigen receptor (IgNAR) variable domain characterized by humanization and structural analysis
Oleg V Kovalenko, Andrea Olland, Nicole Piché-Nicholas, et al.
Bioorganic & Medicinal Chemistry
|
January 5, 2010
Di-substituted pyridinyl aminohydantoins as potent and highly selective human beta-secretase (BACE1) inhibitors
Michael S Malamas, Keith Barnes, Matthew Johnson, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 26, 2009
4-(3-Aryloxyaryl)quinoline sulfones are potent liver X receptor agonists
Ronald C Bernotas, Robert R Singhaus, David H Kaufman, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 6, 2010
Pyridinyl aminohydantoins as small molecule BACE1 inhibitors
Ping Zhou, Yanfang Li, Yi Fan, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 1, 2011
Discovery of a stable macrocyclic o-aminobenzamide Hsp90 inhibitor which significantly decreases tumor volume in a mouse xenograft model
Christoph W Zapf, Jonathan D Bloom, Zhong Li, et al.
Bioorganic & Medicinal Chemistry Letters
|
March 13, 2010
Novel pyrrolyl 2-aminopyridines as potent and selective human beta-secretase (BACE1) inhibitors
Michael S Malamas, Keith Barnes, Yu Hui, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 23, 2019
Inhibition of 3-phosphoglycerate dehydrogenase (PHGDH) by indole amides abrogates de novo serine synthesis in cancer cells
Edouard Mullarky, Jiayi Xu, Anita D Robin, et al.
RSC Medicinal Chemistry
|
April 18, 2022
The identification of highly efficacious functionalised tetrahydrocyclopenta[<i>c</i>]pyrroles as inhibitors of HBV viral replication through modulation of HBV capsid assembly
Andrew G Cole, Steven G Kultgen, Nagraj Mani, et al.
Journal of Medicinal Chemistry
|
August 5, 2005
Synthesis and structure-activity relationship of novel 6-aryl-1,4-dihydrobenzo[d][1,3]oxazine-2-thiones as progesterone receptor modulators leading to the potent and selective nonsteroidal progesterone receptor agonist tanaproget
Andrew Fensome, Reinhold Bender, Rajiv Chopra, et al.
Journal of Medicinal Chemistry
|
September 4, 2024
Rational Design, Synthesis, and Structure-Activity Relationship of a Novel Isoquinolinone-Based Series of HBV Capsid Assembly Modulators Leading to the Identification of Clinical Candidate AB-836
Andrew G Cole, Steven G Kultgen, Nagraj Mani, et al.
Page
of 3