535 results on '"Volpini, Rosaria"'
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102. Simulation and Comparative Analysis of Different Binding Modes of Non-nucleoside Agonists at the A2A Adenosine Receptor
103. The Length and Flexibility of the 2-Substituent of 9-Ethyladenine Derivatives Modulate Affinity and Selectivity for the Human A2AAdenosine Receptor
104. Purinergic P2X receptors: Structural models and analysis of receptor-ligand interaction
105. Antioxidant-Conjugated 1,2,4-Triazolo[4,3-a]pyrazin-3-one Derivatives: Highly Potent and Selective Human A2AAdenosine Receptor Antagonists Possessing Protective Efficacy in Neuropathic Pain
106. Development of new chromatographic tools based on Adenosine A2A subtype receptor for ligand characterization and screening by FAC-MS
107. A2A adenosine receptor ligands: effects on alcohol intake in alcohol-preferring rats
108. New purine derivatives as P2X3 receptor antagonists
109. Functional cAMP assay optimization at CHO cells expressing A2A adenosine receptors and stably transfected with firefly luciferase biosensor
110. Evidence for the existence of a specific G protein-coupled receptor activated by guanosine
111. P2 receptor antagonists prevent synaptic failure and extracellular signal-regulated kinase ½ activation induced by oxygen and glucose deprivation in rat CA1 hippocampus in vitro
112. Medicinal Chemistry of P2X Receptors: Agonists and Orthosteric Antagonists
113. A new ethyladenine antagonist of adenosine A(2A) receptors: behavioral and biochemical characterization as an antiparkinsonian drug
114. Identification of putative guanosine receptor in rat brain
115. Substituted adenine derivatives as novel P2X3 receptor ligands
116. New substituted MECA derivatives as potent and selective agonists for the human adenosine A3 receptor
117. Human adenosine A3 receptor as selective target of new 2-aralkynyl-N6-methyl-MECA derivatives
118. Direct raman measurement of an elevated base pKa in the active site of a small ribozyme in a precatalytic conformation
119. Existence of snoRNA, microRNA, piRNA characteristics in a novel non-coding RNA: x-ncRNA and its biological implication in Homo sapiens
120. Comparison and optimization of transient transfection methods at human astrocytoma cell line 1321N1
121. The 1,2,4-Triazolo[4,3-a]pyrazin-3-one as a Versatile Scaffold for the Design of Potent Adenosine Human Receptor Antagonists. Structural Investigations to Target the A2A Receptor Subtype.
122. Adenosine receptor agonists:synthesis and binding affinity of 2-(aryl)alkylthioadenosine derivatives
123. 2-ChloroATP exerts anti-tumoral actions not mediated by P2 receptors in neuronal and glial cells line
124. Medicinal chemistry and pharmacology of A(2B) adendosine receptors
125. N(6)-alkyl-2-alkynyl derivatives of adenosine as potent and selective agonists at the human adenosine A(3) receptor and a starting point for searching A(2B) ligands
126. Antiviral activity of purine nucleoside analogs against bovine herpesvirus (BHV-1) and maedi visna virus (MVV)
127. Introduction of alkynyl chains on C-8 of adenosine led to very selective antagonists of the A(3) adenosine receptor
128. Synthetic procedure for the preparation of novel potent and selective A(3) adenosine receptor radioligands
129. 3'-Deoxyribofuranose derivatives of 1-deaza and 3-deaza adenosine and their activity as adenosine deaminase inhibitors
130. 'N-Cycloalkylalkyl derivatives of adenosine and 1-deazaadenosine as agonists and partial agonists at the A1 adenosine receptor
131. N-cycloalkyl derivatives of adenosine and 1-deazaadenosine as agonists and partial agonists of the A1 adenosine receptor
132. Synthesis of di- and tri-substituted adenosine derivatives and their affinity at human adenosine receptor subtypes
133. Synthesis and biological activity of a new series of N6-arylcarbamoyl, 2-(Ar)alkynyl-N6-arylcarbamoyl, and N6-carboxamido derivatives of adenosine-5'-N-ethyluronamide as A1 and A3 adenosine receptor agonists
134. Synthesis of new 3’-deoxynucleosides employing the acid-catalyzed fusion method
135. Synthesis and Ability of New Ligands for G Protein-Coupled Receptors 17 (GPR17).
136. Simulation and Comparative Analysis of Different Binding Modes of Non-nucleoside Agonists at the A2A Adenosine Receptor.
137. The Length and Flexibility of the 2-Substituent of 9-Ethyladenine Derivatives Modulate Affinity and Selectivity for the Human A2A Adenosine Receptor.
138. Synthesis and biological activity of 3'-deoxy derivative of 5'-N-methylcarboxamidoadenosine (MECA)
139. Development of new chromatographic tools based on A2A adenosine receptor subtype for ligand characterization and screening by FAC-MS
140. ChemInform Abstract: New 9-Methyl-8-(4-hydroxyphenyl)adenine Derivatives as A1Adenosine Receptor Antagonists.
141. Synthesis and biological evaluation of N6-cycloalkyl derivatives of 1-deazapurine nucleosides: a new class of anti-HIV agents
142. Synthesis and structure-activity relationships of a series of 2-alkynyl-NECA derivatives as selective A2 adenosine receptor agonist
143. Inhibitory effects of 1-deazaadenosine analogs of HIV replication and adenosine deaminase
144. ChemInform Abstract: Neuropeptide S Receptor: Recent Updates on Nonpeptide Antagonist Discovery
145. Effects of A2A adenosine receptor blockade or stimulation on alcohol intake in alcohol-preferring rats
146. Inside Cover: Evidence for the Existence of a Specific G Protein-Coupled Receptor Activated by Guanosine (ChemMedChem 6/2011)
147. Evidence for the Existence of a Specific G Protein-Coupled Receptor Activated by Guanosine
148. Neuropeptide S Receptor: Recent Updates on Nonpeptide Antagonist Discovery
149. New 9-methyl-8-(4-hydroxyphenyl)adenine derivatives as A1 adenosine receptor antagonists
150. 2-Alkynyl derivatives of Adenosine-5'-N-ethyluronamide (NECA): selective A2 adenosine receptor agonists with potent inhibitory activity on Platelet aggregation
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