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C Barrow

Showing results (101-110 of 131) with videos related to

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Neuroreport|February 13, 2009
T-type calcium channels regulate cortical plasticity in-vivo. [corrected]Victor N Uebele, Cindy E Nuss, Vincent P Santarelli, et al.
Nuclear Medicine and Biology|July 12, 2011
[18F]Fluoroazabenzoxazoles as potential amyloid plaque PET tracers: synthesis and in vivo evaluation in rhesus monkeyEric D Hostetler, Sandra Sanabria-Bohórquez, Hong Fan, et al.
Bioorganic & Medicinal Chemistry Letters|January 30, 2002
Discovery of a nonpeptidic small molecule antagonist of the human platelet thrombin receptor (PAR-1)Philippe G Nantermet, James C Barrow, George F Lundell, et al.
Pharmacoepidemiology and Drug Safety|April 8, 2025
Discontinuation Categories Underlying Gaps in Dispensing for Six Medication GroupsElizabeth A Bayliss, Glenn K Goodrich, Jennifer C Barrow, et al.
Chemmedchem|April 27, 2007
Design and synthesis of 2,3,5-substituted imidazolidin-4-one inhibitors of BACE-1James C Barrow, Kenneth E Rittle, Phung L Ngo, et al.
Journal of Medicinal Chemistry|October 2, 2018
Optimization of 8-Hydroxyquinolines as Inhibitors of Catechol O-MethyltransferaseIngrid Buchler, Daniel Akuma, Vinh Au, et al.
Bioorganic & Medicinal Chemistry Letters|May 3, 2016
Synthesis and optimization of N-heterocyclic pyridinones as catechol-O-methyltransferase (COMT) inhibitorsZhijian Zhao, Scott T Harrison, Jeffrey W Schubert, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Synthesis and Evaluation of 5-Fluoro-2-aryloxazolo[5,4-b]pyridines as β-Amyloid PET Ligands and Identification of MK-3328Scott T Harrison, James Mulhearn, Scott E Wolkenberg, et al.
Bioorganic & Medicinal Chemistry Letters|October 10, 2001
Discovery and initial structure-activity relationships of trisubstituted ureas as thrombin receptor (PAR-1) antagonistsJ C Barrow, P G Nantermet, H G Selnick, et al.
Bioorganic & Medicinal Chemistry Letters|September 25, 2003
Unexpected enhancement of thrombin inhibitor potency with o-aminoalkylbenzylamides in the P1 positionKenneth E Rittle, James C Barrow, Kellie J Cutrona, et al.
Pageof 14

Showing results (101-110 of 131) with videos related to

Sort By:
Pageof 14
Neuroreport|February 13, 2009
T-type calcium channels regulate cortical plasticity in-vivo. [corrected]Victor N Uebele, Cindy E Nuss, Vincent P Santarelli, et al.
Nuclear Medicine and Biology|July 12, 2011
[18F]Fluoroazabenzoxazoles as potential amyloid plaque PET tracers: synthesis and in vivo evaluation in rhesus monkeyEric D Hostetler, Sandra Sanabria-Bohórquez, Hong Fan, et al.
Bioorganic & Medicinal Chemistry Letters|January 30, 2002
Discovery of a nonpeptidic small molecule antagonist of the human platelet thrombin receptor (PAR-1)Philippe G Nantermet, James C Barrow, George F Lundell, et al.
Pharmacoepidemiology and Drug Safety|April 8, 2025
Discontinuation Categories Underlying Gaps in Dispensing for Six Medication GroupsElizabeth A Bayliss, Glenn K Goodrich, Jennifer C Barrow, et al.
Chemmedchem|April 27, 2007
Design and synthesis of 2,3,5-substituted imidazolidin-4-one inhibitors of BACE-1James C Barrow, Kenneth E Rittle, Phung L Ngo, et al.
Journal of Medicinal Chemistry|October 2, 2018
Optimization of 8-Hydroxyquinolines as Inhibitors of Catechol O-MethyltransferaseIngrid Buchler, Daniel Akuma, Vinh Au, et al.
Bioorganic & Medicinal Chemistry Letters|May 3, 2016
Synthesis and optimization of N-heterocyclic pyridinones as catechol-O-methyltransferase (COMT) inhibitorsZhijian Zhao, Scott T Harrison, Jeffrey W Schubert, et al.
ACS Medicinal Chemistry Letters|June 6, 2014
Synthesis and Evaluation of 5-Fluoro-2-aryloxazolo[5,4-b]pyridines as β-Amyloid PET Ligands and Identification of MK-3328Scott T Harrison, James Mulhearn, Scott E Wolkenberg, et al.
Bioorganic & Medicinal Chemistry Letters|October 10, 2001
Discovery and initial structure-activity relationships of trisubstituted ureas as thrombin receptor (PAR-1) antagonistsJ C Barrow, P G Nantermet, H G Selnick, et al.
Bioorganic & Medicinal Chemistry Letters|September 25, 2003
Unexpected enhancement of thrombin inhibitor potency with o-aminoalkylbenzylamides in the P1 positionKenneth E Rittle, James C Barrow, Kellie J Cutrona, et al.
Pageof 14