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Shane M Devine

Showing results (11-20 of 30) with videos related to

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Bioorganic & Medicinal Chemistry Letters|August 11, 2007
Dual acting antioxidant A1 adenosine receptor agonistsAlison Gregg, Steven E Bottle, Shane M Devine, et al.
Journal of Medicinal Chemistry|August 7, 2019
The Development Process for Discovery and Clinical Advancement of Modern AntimalarialsTrent D Ashton, Shane M Devine, Jörg J Möhrle, et al.
Bioorganic & Medicinal Chemistry|April 14, 2010
Synthesis and evaluation of new N6-substituted adenosine-5'-N-methylcarboxamides as A3 adenosine receptor agonistsShane M Devine, Alison Gregg, Heidi Figler, et al.
Chemistryopen|April 11, 2015
Design, Synthesis, and Biological Evaluation of Tetra-Substituted Thiophenes as Inhibitors of p38α MAPKNatalie B Vinh, Shane M Devine, Lenka Munoz, et al.
Journal of Medicinal Chemistry|March 22, 2012
Synthesis and pharmacological evaluation of dual acting antioxidant A(2A) adenosine receptor agonistsNicholas E Hausler, Shane M Devine, Fiona M McRobb, et al.
Journal of Medicinal Chemistry|July 29, 2014
Ligand-induced conformational change of Plasmodium falciparum AMA1 detected using 19F NMRXiaopeng Ge, Christopher A MacRaild, Shane M Devine, et al.
ACS Medicinal Chemistry Letters|July 17, 2024
Multiplexed Native Mass Spectrometry Determination of Ligand Selectivity for Fatty Acid-Binding ProteinsMichelle Q Phan, Indu R Chandrashekaran, Naureen Akhtar, et al.
Chemmedchem|June 23, 2021
1,3-Benzodioxole-Modified Noscapine Analogues: Synthesis, Antiproliferative Activity, and Tubulin-Bound StructureCassandra Yong, Shane M Devine, Anne-Catherine Abel, et al.
Molecular & Cellular Proteomics : MCP|December 15, 2019
Multi-omic Characterization of the Mode of Action of a Potent New Antimalarial Compound, JPC-3210, Against <i>Plasmodium falciparum</i>Geoffrey W Birrell, Matthew P Challis, Amanda De Paoli, et al.
Journal of Medicinal Chemistry|February 16, 2018
A Structure-Activity Relationship Study of Bitopic N<sup>6</sup>-Substituted Adenosine Derivatives as Biased Adenosine A<sub>1</sub> Receptor AgonistsLuigi Aurelio, Jo-Anne Baltos, Leigh Ford, et al.
Pageof 3

Showing results (11-20 of 30) with videos related to

Sort By:
Pageof 3
Bioorganic & Medicinal Chemistry Letters|August 11, 2007
Dual acting antioxidant A1 adenosine receptor agonistsAlison Gregg, Steven E Bottle, Shane M Devine, et al.
Journal of Medicinal Chemistry|August 7, 2019
The Development Process for Discovery and Clinical Advancement of Modern AntimalarialsTrent D Ashton, Shane M Devine, Jörg J Möhrle, et al.
Bioorganic & Medicinal Chemistry|April 14, 2010
Synthesis and evaluation of new N6-substituted adenosine-5'-N-methylcarboxamides as A3 adenosine receptor agonistsShane M Devine, Alison Gregg, Heidi Figler, et al.
Chemistryopen|April 11, 2015
Design, Synthesis, and Biological Evaluation of Tetra-Substituted Thiophenes as Inhibitors of p38α MAPKNatalie B Vinh, Shane M Devine, Lenka Munoz, et al.
Journal of Medicinal Chemistry|March 22, 2012
Synthesis and pharmacological evaluation of dual acting antioxidant A(2A) adenosine receptor agonistsNicholas E Hausler, Shane M Devine, Fiona M McRobb, et al.
Journal of Medicinal Chemistry|July 29, 2014
Ligand-induced conformational change of Plasmodium falciparum AMA1 detected using 19F NMRXiaopeng Ge, Christopher A MacRaild, Shane M Devine, et al.
ACS Medicinal Chemistry Letters|July 17, 2024
Multiplexed Native Mass Spectrometry Determination of Ligand Selectivity for Fatty Acid-Binding ProteinsMichelle Q Phan, Indu R Chandrashekaran, Naureen Akhtar, et al.
Chemmedchem|June 23, 2021
1,3-Benzodioxole-Modified Noscapine Analogues: Synthesis, Antiproliferative Activity, and Tubulin-Bound StructureCassandra Yong, Shane M Devine, Anne-Catherine Abel, et al.
Molecular & Cellular Proteomics : MCP|December 15, 2019
Multi-omic Characterization of the Mode of Action of a Potent New Antimalarial Compound, JPC-3210, Against <i>Plasmodium falciparum</i>Geoffrey W Birrell, Matthew P Challis, Amanda De Paoli, et al.
Journal of Medicinal Chemistry|February 16, 2018
A Structure-Activity Relationship Study of Bitopic N<sup>6</sup>-Substituted Adenosine Derivatives as Biased Adenosine A<sub>1</sub> Receptor AgonistsLuigi Aurelio, Jo-Anne Baltos, Leigh Ford, et al.
Pageof 3