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Ann M Decker

Showing results (51-60 of 86) with videos related to

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Translational Oncology|May 4, 2020
Adrenergic Blockade Promotes Maintenance of Dormancy in Prostate Cancer Through Upregulation of GAS6Ann M Decker, Joseph T Decker, Younghun Jung, et al.
Bioorganic & Medicinal Chemistry|May 20, 2021
Rational design of cannabinoid type-1 receptor allosteric modulators: Org27569 and PSNCBAM-1 hybridsThuy Nguyen, Thomas F Gamage, Ann M Decker, et al.
ACS Chemical Neuroscience|December 12, 2023
Design, Synthesis, and Structure-Activity Relationship Studies of Novel GPR88 Agonists (4-Substituted-phenyl)acetamides Based on the Reversed Amide ScaffoldMd Toufiqur Rahman, Dongliang Guan, Hetti Handi Chaminda Lakmal, et al.
Bioorganic & Medicinal Chemistry|July 29, 2015
The importance of the 6- and 7-positions of tetrahydroisoquinolines as selective antagonists for the orexin 1 receptorDavid A Perrey, Ann M Decker, Jun-Xu Li, et al.
Journal of Medicinal Chemistry|December 2, 2021
Indole-Containing Amidinohydrazones as Nonpeptide, Dual RXFP3/4 Agonists: Synthesis, Structure-Activity Relationship, and Molecular Modeling StudiesDongliang Guan, Md Toufiqur Rahman, Elaine A Gay, et al.
Bioorganic & Medicinal Chemistry|July 2, 2016
Design, synthesis, and pharmacological evaluation of JDTic analogs to examine the significance of replacement of the 3-hydroxyphenyl group with pyridine or thiophene bioisosteresChad M Kormos, Moses G Gichinga, Scott P Runyon, et al.
ACS Medicinal Chemistry Letters|July 26, 2017
Simple Tetrahydroisoquinolines Are Potent and Selective Kappa Opioid Receptor AntagonistsChad M Kormos, Pauline W Ondachi, Scott P Runyon, et al.
Journal of Medicinal Chemistry|April 8, 2025
Development of Squaramides as Allosteric Modulators of the CB<sub>1</sub> Receptor: Synthesis, Computational Studies, Biological Characterization, and Effects against Cocaine-Induced Behavioral Sensitization and Reinstatement in RatsThuy Nguyen, Ann M Decker, Daniel G Barrus, et al.
ACS Chemical Neuroscience|July 25, 2017
Discovery of Novel Proline-Based Neuropeptide FF Receptor AntagonistsThuy Nguyen, Ann M Decker, Tiffany L Langston, et al.
Journal of Medicinal Chemistry|February 7, 2023
Improvement of the Metabolic Stability of GPR88 Agonist RTI-13951-33: Design, Synthesis, and Biological EvaluationMd Toufiqur Rahman, Ann M Decker, Sami Ben Hamida, et al.
Pageof 9

Showing results (51-60 of 86) with videos related to

Sort By:
Pageof 9
Translational Oncology|May 4, 2020
Adrenergic Blockade Promotes Maintenance of Dormancy in Prostate Cancer Through Upregulation of GAS6Ann M Decker, Joseph T Decker, Younghun Jung, et al.
Bioorganic & Medicinal Chemistry|May 20, 2021
Rational design of cannabinoid type-1 receptor allosteric modulators: Org27569 and PSNCBAM-1 hybridsThuy Nguyen, Thomas F Gamage, Ann M Decker, et al.
ACS Chemical Neuroscience|December 12, 2023
Design, Synthesis, and Structure-Activity Relationship Studies of Novel GPR88 Agonists (4-Substituted-phenyl)acetamides Based on the Reversed Amide ScaffoldMd Toufiqur Rahman, Dongliang Guan, Hetti Handi Chaminda Lakmal, et al.
Bioorganic & Medicinal Chemistry|July 29, 2015
The importance of the 6- and 7-positions of tetrahydroisoquinolines as selective antagonists for the orexin 1 receptorDavid A Perrey, Ann M Decker, Jun-Xu Li, et al.
Journal of Medicinal Chemistry|December 2, 2021
Indole-Containing Amidinohydrazones as Nonpeptide, Dual RXFP3/4 Agonists: Synthesis, Structure-Activity Relationship, and Molecular Modeling StudiesDongliang Guan, Md Toufiqur Rahman, Elaine A Gay, et al.
Bioorganic & Medicinal Chemistry|July 2, 2016
Design, synthesis, and pharmacological evaluation of JDTic analogs to examine the significance of replacement of the 3-hydroxyphenyl group with pyridine or thiophene bioisosteresChad M Kormos, Moses G Gichinga, Scott P Runyon, et al.
ACS Medicinal Chemistry Letters|July 26, 2017
Simple Tetrahydroisoquinolines Are Potent and Selective Kappa Opioid Receptor AntagonistsChad M Kormos, Pauline W Ondachi, Scott P Runyon, et al.
Journal of Medicinal Chemistry|April 8, 2025
Development of Squaramides as Allosteric Modulators of the CB<sub>1</sub> Receptor: Synthesis, Computational Studies, Biological Characterization, and Effects against Cocaine-Induced Behavioral Sensitization and Reinstatement in RatsThuy Nguyen, Ann M Decker, Daniel G Barrus, et al.
ACS Chemical Neuroscience|July 25, 2017
Discovery of Novel Proline-Based Neuropeptide FF Receptor AntagonistsThuy Nguyen, Ann M Decker, Tiffany L Langston, et al.
Journal of Medicinal Chemistry|February 7, 2023
Improvement of the Metabolic Stability of GPR88 Agonist RTI-13951-33: Design, Synthesis, and Biological EvaluationMd Toufiqur Rahman, Ann M Decker, Sami Ben Hamida, et al.
Pageof 9