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Bioorganic & Medicinal Chemistry Letters
|
October 19, 2010
Antimalarial histone deacetylase inhibitors containing cinnamate or NSAID components
Nicole C Wheatley, Katherine T Andrews, Truc L Tran, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
September 19, 2019
Computer Modelling and Synthesis of Deoxy and Monohydroxy Analogues of a Ribitylaminouracil Bacterial Metabolite that Potently Activates Human T Cells
Geraldine J M Ler, Weijun Xu, Jeffrey Y W Mak, et al.
The Journal of Surgical Research
|
January 21, 2004
Protective effects of a potent C5a receptor antagonist on experimental acute limb ischemia-reperfusion in rats
Trent M Woodruff, Thiruma V Arumugam, Ian A Shiels, et al.
Journal of Medicinal Chemistry
|
March 19, 2004
Countering cooperative effects in protease inhibitors using constrained beta-strand-mimicking templates in focused combinatorial libraries
Robert C Reid, Leonard K Pattenden, Joel D A Tyndall, et al.
The Journal of Surgical Research
|
April 2, 2002
Protective effect of a new C5a receptor antagonist against ischemia-reperfusion injury in the rat small intestine
Thiruma V Arumugam, Ian A Shiels, Trent M Woodruff, 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.
Inorganic Chemistry
|
September 16, 2008
Linkage isomerism in the binding of pentapeptide Ac-His(Ala)3His-NH2 to (ethylenediamine)palladium(II): effect of the binding mode on peptide conformation
Huy N Hoang, Gavin K Bryant, Michael J Kelso, 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.
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.
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of 33
Search research articles
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Showing results (111-120 of 326) with videos related to
Sort By:
Page
of 33
Bioorganic & Medicinal Chemistry Letters
|
October 19, 2010
Antimalarial histone deacetylase inhibitors containing cinnamate or NSAID components
Nicole C Wheatley, Katherine T Andrews, Truc L Tran, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)
|
September 19, 2019
Computer Modelling and Synthesis of Deoxy and Monohydroxy Analogues of a Ribitylaminouracil Bacterial Metabolite that Potently Activates Human T Cells
Geraldine J M Ler, Weijun Xu, Jeffrey Y W Mak, et al.
The Journal of Surgical Research
|
January 21, 2004
Protective effects of a potent C5a receptor antagonist on experimental acute limb ischemia-reperfusion in rats
Trent M Woodruff, Thiruma V Arumugam, Ian A Shiels, et al.
Journal of Medicinal Chemistry
|
March 19, 2004
Countering cooperative effects in protease inhibitors using constrained beta-strand-mimicking templates in focused combinatorial libraries
Robert C Reid, Leonard K Pattenden, Joel D A Tyndall, et al.
The Journal of Surgical Research
|
April 2, 2002
Protective effect of a new C5a receptor antagonist against ischemia-reperfusion injury in the rat small intestine
Thiruma V Arumugam, Ian A Shiels, Trent M Woodruff, 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.
Inorganic Chemistry
|
September 16, 2008
Linkage isomerism in the binding of pentapeptide Ac-His(Ala)3His-NH2 to (ethylenediamine)palladium(II): effect of the binding mode on peptide conformation
Huy N Hoang, Gavin K Bryant, Michael J Kelso, 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.
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.
Page
of 33