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Publications by Letizia Trincavelli
The Identification of the 2-Phenylphthalazin-1(2h)-One Scaffold as a New Decorable Core Skeleton for the Design of Potent and Selective Human A3Adenosine Receptor Antagonists
Journal of Medicinal Chemistry
Drug Discovery
Molecular Medicine
Related publications
“Reversine” and Its 2-Substituted Adenine Derivatives as Potent and Selective A3Adenosine Receptor Antagonists
Journal of Medicinal Chemistry
Drug Discovery
Molecular Medicine
4-Amido-2-Aryl-1, 2, 4-Triazolo[4, 3-A]quinoxalin-1-Ones as New Potent and Selective Human A3 Adenosine Receptor Antagonists. Synthesis, Pharmacological Evaluation, and Ligand-Receptor Modeling Studies
Potent, Selective, and Orally Efficacious Antagonists of Melanin-Concentrating Hormone Receptor 1
Tricyclic Imidazoline Derivatives as Potent and Selective Adenosine A1 Receptor Antagonists
SST3-selective Potent Peptidic Somatostatin Receptor Antagonists
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
4-Aryliden-2-Methyloxazol-5(4h)-One as a New Scaffold for Selective Reversible MAGL Inhibitors
Journal of Enzyme Inhibition and Medicinal Chemistry
Medicine
Drug Discovery
Pharmacology
Structure−Activity Relationships of Truncatedd- Andl-4′-Thioadenosine Derivatives as Species-Independent A3Adenosine Receptor Antagonists(1)
Journal of Medicinal Chemistry
Drug Discovery
Molecular Medicine
2‐Phenyloxazole‐4‐carboxamide as New Scaffold for Selective Inhibition of Human Monoamine Oxidase B
ChemMedChem
Organic Chemistry
Molecular Medicine
Pharmacology
Biochemistry
Toxicology
Drug Discovery
Pharmaceutics
Design, Synthesis and Pharmacological Evaluation of Indolylsulfonamide Amines as Potent and Selective 5-HT6receptor Antagonists
Journal of Enzyme Inhibition and Medicinal Chemistry
Medicine
Drug Discovery
Pharmacology
