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ACS Chemical Neuroscience
|
March 24, 2022
Identification of a Potent Human Trace Amine-Associated Receptor 1 Antagonist
Ann M Decker, Marcus F Brackeen, Aida Mohammadkhani, et al.
The Prostate
|
July 14, 2020
CXCL12γ induces human prostate and mammary gland development
Younghun Jung, Jin Koo Kim, Eunsohl Lee, et al.
Journal of Medicinal Chemistry
|
August 28, 2014
Diarylureas as allosteric modulators of the cannabinoid CB1 receptor: structure-activity relationship studies on 1-(4-chlorophenyl)-3-{3-[6-(pyrrolidin-1-yl)pyridin-2-yl]phenyl}urea (PSNCBAM-1)
Nadezhda German, Ann M Decker, Brian P Gilmour, et al.
Journal of Biomedical Science
|
March 29, 2017
Development and validation of a high-throughput calcium mobilization assay for the orphan receptor GPR88
Ann M Decker, Elaine A Gay, Kelly M Mathews, et al.
Addiction Biology
|
October 27, 2022
The GPR88 agonist RTI-13951-33 reduces alcohol drinking and seeking in mice
Sami Ben Hamida, Michelle Carter, Emmanuel Darcq, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 7, 2014
Alpha-ethyltryptamines as dual dopamine-serotonin releasers
Bruce E Blough, Antonio Landavazo, John S Partilla, et al.
Neuropharmacology
|
March 5, 2018
Comparative neuropharmacology of N-(2-methoxybenzyl)-2,5-dimethoxyphenethylamine (NBOMe) hallucinogens and their 2C counterparts in male rats
Joshua S Elmore, Ann M Decker, Agnieszka Sulima, et al.
Psychopharmacology
|
October 21, 2018
The dopamine, serotonin and norepinephrine releasing activities of a series of methcathinone analogs in male rat brain synaptosomes
Bruce E Blough, Ann M Decker, Antonio Landavazo, et al.
ACS Medicinal Chemistry Letters
|
June 20, 2014
Hybrid dopamine uptake blocker-serotonin releaser ligands: a new twist on transporter-focused therapeutics
Bruce E Blough, Antonio Landavazo, John S Partilla, et al.
Journal of Medicinal Chemistry
|
October 10, 2019
Synthesis and Pharmacological Evaluation of 1-Phenyl-3-Thiophenylurea Derivatives as Cannabinoid Type-1 Receptor Allosteric Modulators
Thuy Nguyen, Thomas F Gamage, Ann M Decker, et al.
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of 9
Search research articles
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Showing results (31-40 of 86) with videos related to
Sort By:
Page
of 9
ACS Chemical Neuroscience
|
March 24, 2022
Identification of a Potent Human Trace Amine-Associated Receptor 1 Antagonist
Ann M Decker, Marcus F Brackeen, Aida Mohammadkhani, et al.
The Prostate
|
July 14, 2020
CXCL12γ induces human prostate and mammary gland development
Younghun Jung, Jin Koo Kim, Eunsohl Lee, et al.
Journal of Medicinal Chemistry
|
August 28, 2014
Diarylureas as allosteric modulators of the cannabinoid CB1 receptor: structure-activity relationship studies on 1-(4-chlorophenyl)-3-{3-[6-(pyrrolidin-1-yl)pyridin-2-yl]phenyl}urea (PSNCBAM-1)
Nadezhda German, Ann M Decker, Brian P Gilmour, et al.
Journal of Biomedical Science
|
March 29, 2017
Development and validation of a high-throughput calcium mobilization assay for the orphan receptor GPR88
Ann M Decker, Elaine A Gay, Kelly M Mathews, et al.
Addiction Biology
|
October 27, 2022
The GPR88 agonist RTI-13951-33 reduces alcohol drinking and seeking in mice
Sami Ben Hamida, Michelle Carter, Emmanuel Darcq, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 7, 2014
Alpha-ethyltryptamines as dual dopamine-serotonin releasers
Bruce E Blough, Antonio Landavazo, John S Partilla, et al.
Neuropharmacology
|
March 5, 2018
Comparative neuropharmacology of N-(2-methoxybenzyl)-2,5-dimethoxyphenethylamine (NBOMe) hallucinogens and their 2C counterparts in male rats
Joshua S Elmore, Ann M Decker, Agnieszka Sulima, et al.
Psychopharmacology
|
October 21, 2018
The dopamine, serotonin and norepinephrine releasing activities of a series of methcathinone analogs in male rat brain synaptosomes
Bruce E Blough, Ann M Decker, Antonio Landavazo, et al.
ACS Medicinal Chemistry Letters
|
June 20, 2014
Hybrid dopamine uptake blocker-serotonin releaser ligands: a new twist on transporter-focused therapeutics
Bruce E Blough, Antonio Landavazo, John S Partilla, et al.
Journal of Medicinal Chemistry
|
October 10, 2019
Synthesis and Pharmacological Evaluation of 1-Phenyl-3-Thiophenylurea Derivatives as Cannabinoid Type-1 Receptor Allosteric Modulators
Thuy Nguyen, Thomas F Gamage, Ann M Decker, et al.
Page
of 9