Substituted acyclic sulfonamides as human cannabinoid-1 receptor inverse agonists (original) (raw)

Synthesis and evaluation of N-[(1S,2S)-3-(4-chlorophenyl)-2-(3-cyanophenyl)-1-methylpropyl]-2-methyl-2-aminopropanamide as human cannabinoid-1 receptor (CB1R) inverse agonists

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Bioorganic & Medicinal Chemistry Letters, 2009

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Pyridopyrimidine based cannabinoid-1 receptor inverse agonists: Synthesis and biological evaluation

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Optimization of triaryl bis-sulfones as cannabinoid-2 receptor ligands

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New bicyclic cannabinoid receptor-1 (CB1-R) antagonists

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Bioorganic & Medicinal Chemistry Letters, 2006

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Novel sulfenamides and sulfonamides based on pyridazinone and pyridazine scaffolds as CB 1 receptor ligand antagonists

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Bioorganic & Medicinal Chemistry, 2018

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Synthesis and Characterization of NESS 0327: A Novel Putative Antagonist of the CB1 Cannabinoid Receptor

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Journal of Pharmacology and Experimental Therapeutics, 2003

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Chemical Synthesis, Pharmacokinetic Properties and Biological Effects of JM-00266, a Putative Non-Brain Penetrant Cannabinoid Receptor 1 Inverse Agonist

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International Journal of Molecular Sciences, 2022

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Discovery of potent and orally bioavailable heterocycle-based cannabinoid CB1 receptor agonists

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Bioorganic & Medicinal Chemistry Letters, 2011

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CB2 selective sulfamoyl benzamides: Optimization of the amide functionality

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1-Benzhydryl-3-phenylurea and 1-Benzhydryl-3-phenylthiourea Derivatives: New Templates among the CB 1 Cannabinoid Receptor Inverse Agonists

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Journal of Medicinal Chemistry, 2005

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Bioisosteric replacement of the hydrazide pharmacophore of the cannabinoid-1 receptor antagonist SR141716A. Part I: Potent, orally-active 1,4-disubstituted imidazoles

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Bioorganic & Medicinal Chemistry Letters, 2009

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Evaluation of carboxamide-type synthetic cannabinoids as CB1/CB2 receptor agonists: difference between the enantiomers

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Forensic Toxicology, 2017

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N-acyl-dopamines: novel synthetic CB1 cannabinoid-receptor ligands and inhibitors of anandamide inactivation with cannabimimetic activity in vitro and in vivo

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Arachidonylsulfonyl derivatives as cannabinoid CB1 receptor and fatty acid amide hydrolase inhibitors

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Bioorganic & Medicinal Chemistry Letters, 2003

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Design and synthesis of the CB1 selective cannabinoid antagonist AM281: A potential human SPECT ligand

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AAPS PharmSci, 1999

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Design, synthesis, and pharmacological characterization of indol-3-ylacetamides, indol-3-yloxoacetamides, and indol-3-ylcarboxamides: potent and selective CB2 cannabinoid receptor inverse agonists

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Journal of medicinal chemistry, 2012

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Discovery of 7-Oxopyrazolo[1,5- a ]pyrimidine-6-carboxamides as Potent and Selective CB 2 Cannabinoid Receptor Inverse Agonists

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A Pyridone Analogue of Traditional Cannabinoids. A New Class of Selective Ligands for the CB2 Receptor

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New Pyridone-Based Derivatives as Cannabinoid Receptor Type 2 Agonists

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Diaryl Piperidines As CB1 Receptor Antagonists

Yan Xia

Bioorganic & medicinal …, 2010

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New pyridazinone-4-carboxamides as new cannabinoid receptor type-2 inverse agonists: Synthesis, pharmacological data and molecular docking

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Discovery of N-(3-(morpholinomethyl)-phenyl)-amides as potent and selective CB2 agonists

Damian Weaver

Bioorganic & Medicinal Chemistry Letters, 2009

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The therapeutic applications of cannabinoid agonists and antagonists

François Petitet

Emerging Drugs, 1998

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Triaryl bis-sulfones as cannabinoid-2 receptor ligands: SAR studies

Neng-Yang Shih

Bioorganic & Medicinal Chemistry Letters, 2005

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