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Organic & Biomolecular Chemistry
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March 8, 2012
Relaxation of the rigid backbone of an oligoamide-foldamer-based α-helix mimetic: identification of potent Bcl-xL inhibitors
Jeremy L Yap, Xiaobo Cao, Kenno Vanommeslaeghe, et al.
BMC Cancer
|
November 23, 2012
The downregulation of Mcl-1 via USP9X inhibition sensitizes solid tumors to Bcl-xl inhibition
Chander Peddaboina, Daniel Jupiter, Steven Fletcher, et al.
Oncotarget
|
June 27, 2013
Disruption of Myc-Max heterodimerization with improved cell-penetrating analogs of the small molecule 10074-G5
Huabo Wang, Jay Chauhan, Angela Hu, et al.
Oncotarget
|
November 13, 2018
Erratum: Disruption of Myc-Max Heterodimerization with Improved Cell-Penetrating Analogs of the Small Molecule 10074-G5
Huabo Wang, Jay Chauhan, Angela Hu, et al.
Journal of Medicinal Chemistry
|
March 4, 2015
Perturbation of the c-Myc-Max protein-protein interaction via synthetic α-helix mimetics
Kwan-Young Jung, Huabo Wang, Peter Teriete, et al.
SLAS Discovery : Advancing Life Sciences R & D
|
June 25, 2024
Profiling cells with DELs: Small molecule fingerprinting of cell surfaces
Jason Deng, Svetlana Belyanskaya, Ninad Prabhu, et al.
Molecular Cancer
|
May 18, 2013
The novel BH3 α-helix mimetic JY-1-106 induces apoptosis in a subset of cancer cells (lung cancer, colon cancer and mesothelioma) by disrupting Bcl-xL and Mcl-1 protein-protein interactions with Bak
Xiaobo Cao, Jeremy L Yap, M Karen Newell-Rogers, et al.
Organic & Biomolecular Chemistry
|
April 30, 2013
Structural modifications of (Z)-3-(2-aminoethyl)-5-(4-ethoxybenzylidene)thiazolidine-2,4-dione that improve selectivity for inhibiting the proliferation of melanoma cells containing active ERK signaling
Kwan-Young Jung, Ramin Samadani, Jay Chauhan, et al.
European Journal of Medicinal Chemistry
|
March 18, 2016
Structure-based design of N-substituted 1-hydroxy-4-sulfamoyl-2-naphthoates as selective inhibitors of the Mcl-1 oncoprotein
Maryanna E Lanning, Wenbo Yu, Jeremy L Yap, et al.
ACS Medicinal Chemistry Letters
|
June 17, 2026
Structure-Guided Discovery of Selective Polo-Like Kinase 3 Inhibitors
Jeremy L Yap, Gabrielle Lovett, Jeremy W Mason, et al.
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Search research articles
Search
Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
Organic & Biomolecular Chemistry
|
March 8, 2012
Relaxation of the rigid backbone of an oligoamide-foldamer-based α-helix mimetic: identification of potent Bcl-xL inhibitors
Jeremy L Yap, Xiaobo Cao, Kenno Vanommeslaeghe, et al.
BMC Cancer
|
November 23, 2012
The downregulation of Mcl-1 via USP9X inhibition sensitizes solid tumors to Bcl-xl inhibition
Chander Peddaboina, Daniel Jupiter, Steven Fletcher, et al.
Oncotarget
|
June 27, 2013
Disruption of Myc-Max heterodimerization with improved cell-penetrating analogs of the small molecule 10074-G5
Huabo Wang, Jay Chauhan, Angela Hu, et al.
Oncotarget
|
November 13, 2018
Erratum: Disruption of Myc-Max Heterodimerization with Improved Cell-Penetrating Analogs of the Small Molecule 10074-G5
Huabo Wang, Jay Chauhan, Angela Hu, et al.
Journal of Medicinal Chemistry
|
March 4, 2015
Perturbation of the c-Myc-Max protein-protein interaction via synthetic α-helix mimetics
Kwan-Young Jung, Huabo Wang, Peter Teriete, et al.
SLAS Discovery : Advancing Life Sciences R & D
|
June 25, 2024
Profiling cells with DELs: Small molecule fingerprinting of cell surfaces
Jason Deng, Svetlana Belyanskaya, Ninad Prabhu, et al.
Molecular Cancer
|
May 18, 2013
The novel BH3 α-helix mimetic JY-1-106 induces apoptosis in a subset of cancer cells (lung cancer, colon cancer and mesothelioma) by disrupting Bcl-xL and Mcl-1 protein-protein interactions with Bak
Xiaobo Cao, Jeremy L Yap, M Karen Newell-Rogers, et al.
Organic & Biomolecular Chemistry
|
April 30, 2013
Structural modifications of (Z)-3-(2-aminoethyl)-5-(4-ethoxybenzylidene)thiazolidine-2,4-dione that improve selectivity for inhibiting the proliferation of melanoma cells containing active ERK signaling
Kwan-Young Jung, Ramin Samadani, Jay Chauhan, et al.
European Journal of Medicinal Chemistry
|
March 18, 2016
Structure-based design of N-substituted 1-hydroxy-4-sulfamoyl-2-naphthoates as selective inhibitors of the Mcl-1 oncoprotein
Maryanna E Lanning, Wenbo Yu, Jeremy L Yap, et al.
ACS Medicinal Chemistry Letters
|
June 17, 2026
Structure-Guided Discovery of Selective Polo-Like Kinase 3 Inhibitors
Jeremy L Yap, Gabrielle Lovett, Jeremy W Mason, et al.
Page
of 3