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RSC Chemical Biology
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July 22, 2022
Landscaping macrocyclic peptides: stapling hDM2-binding peptides for helicity, protein affinity, proteolytic stability and cell uptake
Aline D de Araujo, Junxian Lim, Kai-Chen Wu, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
December 22, 2017
A Potent Antagonist of Protease-Activated Receptor 2 That Inhibits Multiple Signaling Functions in Human Cancer Cells
Yuhong Jiang, Mei-Kwan Yau, Junxian Lim, et al.
Journal of Medicinal Chemistry
|
May 9, 2020
Achiral Derivatives of Hydroxamate AR-42 Potently Inhibit Class I HDAC Enzymes and Cancer Cell Proliferation
Jiahui Tng, Junxian Lim, Kai-Chen Wu, et al.
Journal of Medicinal Chemistry
|
September 27, 2014
Potent heterocyclic ligands for human complement c3a receptor
Robert C Reid, Mei-Kwan Yau, Ranee Singh, et al.
Bioconjugate Chemistry
|
June 1, 2017
Europium-Labeled Synthetic C3a Protein as a Novel Fluorescent Probe for Human Complement C3a Receptor
Aline Dantas de Araujo, Chongyang Wu, Kai-Chen Wu, et al.
Journal of Medicinal Chemistry
|
September 12, 2009
Structure-activity relationships for substrate-based inhibitors of human complement factor B
Gloria Ruiz-Gómez, Junxian Lim, Maria A Halili, et al.
Journal of Medicinal Chemistry
|
March 28, 2018
Bicyclic Helical Peptides as Dual Inhibitors Selective for Bcl2A1 and Mcl-1 Proteins
Aline D de Araujo, Junxian Lim, Kai-Chen Wu, et al.
Chemical Communications (Cambridge, England)
|
October 24, 2022
Helical structure in cyclic peptides: effect of <i>N</i>-methyl amides <i>versus</i> esters
Chongyang Wu, Huy N Hoang, Timothy A Hill, et al.
British Journal of Pharmacology
|
February 26, 2010
Antifibrotic activity of an inhibitor of histone deacetylases in DOCA-salt hypertensive rats
Abishek Iyer, Andrew Fenning, Junxian Lim, et al.
British Journal of Pharmacology
|
September 3, 2024
A novel inhibitor of class IIa histone deacetylases attenuates collagen-induced arthritis
Eunice K Poon, Ligong Liu, Kai-Chen Wu, et al.
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of 5
Search research articles
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Showing results (11-20 of 41) with videos related to
Sort By:
Page
of 5
RSC Chemical Biology
|
July 22, 2022
Landscaping macrocyclic peptides: stapling hDM2-binding peptides for helicity, protein affinity, proteolytic stability and cell uptake
Aline D de Araujo, Junxian Lim, Kai-Chen Wu, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
December 22, 2017
A Potent Antagonist of Protease-Activated Receptor 2 That Inhibits Multiple Signaling Functions in Human Cancer Cells
Yuhong Jiang, Mei-Kwan Yau, Junxian Lim, et al.
Journal of Medicinal Chemistry
|
May 9, 2020
Achiral Derivatives of Hydroxamate AR-42 Potently Inhibit Class I HDAC Enzymes and Cancer Cell Proliferation
Jiahui Tng, Junxian Lim, Kai-Chen Wu, et al.
Journal of Medicinal Chemistry
|
September 27, 2014
Potent heterocyclic ligands for human complement c3a receptor
Robert C Reid, Mei-Kwan Yau, Ranee Singh, et al.
Bioconjugate Chemistry
|
June 1, 2017
Europium-Labeled Synthetic C3a Protein as a Novel Fluorescent Probe for Human Complement C3a Receptor
Aline Dantas de Araujo, Chongyang Wu, Kai-Chen Wu, et al.
Journal of Medicinal Chemistry
|
September 12, 2009
Structure-activity relationships for substrate-based inhibitors of human complement factor B
Gloria Ruiz-Gómez, Junxian Lim, Maria A Halili, et al.
Journal of Medicinal Chemistry
|
March 28, 2018
Bicyclic Helical Peptides as Dual Inhibitors Selective for Bcl2A1 and Mcl-1 Proteins
Aline D de Araujo, Junxian Lim, Kai-Chen Wu, et al.
Chemical Communications (Cambridge, England)
|
October 24, 2022
Helical structure in cyclic peptides: effect of <i>N</i>-methyl amides <i>versus</i> esters
Chongyang Wu, Huy N Hoang, Timothy A Hill, et al.
British Journal of Pharmacology
|
February 26, 2010
Antifibrotic activity of an inhibitor of histone deacetylases in DOCA-salt hypertensive rats
Abishek Iyer, Andrew Fenning, Junxian Lim, et al.
British Journal of Pharmacology
|
September 3, 2024
A novel inhibitor of class IIa histone deacetylases attenuates collagen-induced arthritis
Eunice K Poon, Ligong Liu, Kai-Chen Wu, et al.
Page
of 5