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Charles W Locuson

Showing results (31-40 of 37) with videos related to

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Chemmedchem|September 12, 2014
Discovery of a highly selective PLD2 inhibitor (ML395): a new probe with improved physiochemical properties and broad-spectrum antiviral activity against influenza strainsMatthew C O'Reilly, Thomas H Oguin, Sarah A Scott, et al.
Bioorganic & Medicinal Chemistry Letters|August 31, 2016
Optimization of the choline transporter (CHT) inhibitor ML352: Development of VU6001221, an improved in vivo tool compoundJeanette L Bertron, Elizabeth A Ennis, Christopher J Tarr, et al.
Journal of Medicinal Chemistry|October 2, 2015
Development of Novel, CNS Penetrant Positive Allosteric Modulators for the Metabotropic Glutamate Receptor Subtype 1 (mGlu1), Based on an N-(3-Chloro-4-(1,3-dioxoisoindolin-2-yl)phenyl)-3-methylfuran-2-carboxamide Scaffold, That Potentiate Wild Type and Mutant mGlu1 Receptors Found in SchizophrenicsPedro M Garcia-Barrantes, Hyekyung P Cho, Colleen M Niswender, et al.
The Journal of Infectious Diseases|April 18, 2015
VFV as a New Effective CYP51 Structure-Derived Drug Candidate for Chagas Disease and Visceral LeishmaniasisGalina I Lepesheva, Tatiana Y Hargrove, Girish Rachakonda, et al.
Bioorganic & Medicinal Chemistry Letters|September 2, 2014
Substituted indoles as selective protease activated receptor 4 (PAR-4) antagonists: Discovery and SAR of ML354Wandong Wen, Summer E Young, Matthew T Duvernay, et al.
Journal of Medicinal Chemistry|November 3, 2015
Design of 4-Oxo-1-aryl-1,4-dihydroquinoline-3-carboxamides as Selective Negative Allosteric Modulators of Metabotropic Glutamate Receptor Subtype 2Andrew S Felts, Alice L Rodriguez, Katrina A Smith, et al.
ACS Chemical Neuroscience|April 22, 2018
Discovery and Optimization of Potent and CNS Penetrant M<sub>5</sub>-Preferring Positive Allosteric Modulators Derived from a Novel, Chiral N-(Indanyl)piperidine Amide ScaffoldAaron M Bender, Hyekyung P Cho, Kellie D Nance, et al.
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Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Chemmedchem|September 12, 2014
Discovery of a highly selective PLD2 inhibitor (ML395): a new probe with improved physiochemical properties and broad-spectrum antiviral activity against influenza strainsMatthew C O'Reilly, Thomas H Oguin, Sarah A Scott, et al.
Bioorganic & Medicinal Chemistry Letters|August 31, 2016
Optimization of the choline transporter (CHT) inhibitor ML352: Development of VU6001221, an improved in vivo tool compoundJeanette L Bertron, Elizabeth A Ennis, Christopher J Tarr, et al.
Journal of Medicinal Chemistry|October 2, 2015
Development of Novel, CNS Penetrant Positive Allosteric Modulators for the Metabotropic Glutamate Receptor Subtype 1 (mGlu1), Based on an N-(3-Chloro-4-(1,3-dioxoisoindolin-2-yl)phenyl)-3-methylfuran-2-carboxamide Scaffold, That Potentiate Wild Type and Mutant mGlu1 Receptors Found in SchizophrenicsPedro M Garcia-Barrantes, Hyekyung P Cho, Colleen M Niswender, et al.
The Journal of Infectious Diseases|April 18, 2015
VFV as a New Effective CYP51 Structure-Derived Drug Candidate for Chagas Disease and Visceral LeishmaniasisGalina I Lepesheva, Tatiana Y Hargrove, Girish Rachakonda, et al.
Bioorganic & Medicinal Chemistry Letters|September 2, 2014
Substituted indoles as selective protease activated receptor 4 (PAR-4) antagonists: Discovery and SAR of ML354Wandong Wen, Summer E Young, Matthew T Duvernay, et al.
Journal of Medicinal Chemistry|November 3, 2015
Design of 4-Oxo-1-aryl-1,4-dihydroquinoline-3-carboxamides as Selective Negative Allosteric Modulators of Metabotropic Glutamate Receptor Subtype 2Andrew S Felts, Alice L Rodriguez, Katrina A Smith, et al.
ACS Chemical Neuroscience|April 22, 2018
Discovery and Optimization of Potent and CNS Penetrant M<sub>5</sub>-Preferring Positive Allosteric Modulators Derived from a Novel, Chiral N-(Indanyl)piperidine Amide ScaffoldAaron M Bender, Hyekyung P Cho, Kellie D Nance, et al.
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