13 articles for ML Trincavelli
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
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Further studies on pyrazolo[1',5':1,6]pyrimido[4,5-d]pyridazin-4(3H)-ones as potent and selective human A1 adenosine receptor antagonists.

Universita Degli Studi Di Firenze
Combining galantamine and memantine in multitargeted, new chemical entities potentially useful in Alzheimer's disease.

Istituto Italiano Di Tecnologia
3-aryl-[1,2,4]triazino[4,3-a]benzimidazol-4(10H)-one: a novel template for the design of highly selective A2B adenosine receptor antagonists.

University of Pisa
Novel N2-substituted pyrazolo[3,4-d]pyrimidine adenosine A3 receptor antagonists: inhibition of A3-mediated human glioblastoma cell proliferation.

University of Pisa
Structure-based optimization of pyrazolo[3,4-d]pyrimidines as Abl inhibitors and antiproliferative agents toward human leukemia cell lines.

University of Siena
5-amino-2-phenyl[1,2,3]triazolo[1,2-a][1,2,4]benzotriazin-1-one: a versatile scaffold to obtain potent and selective A3 adenosine receptor antagonists.

University of Pisa
2-(Benzimidazol-2-yl)quinoxalines: a novel class of selective antagonists at human A(1) and A(3) adenosine receptors designed by 3D database searching.

University of Naples Federico II
Frontal affinity chromatography-mass spectrometry useful for characterization of new ligands for GPR17 receptor.

University of Pavia
Synthesis and 3D QSAR of new pyrazolo[3,4-b]pyridines: potent and selective inhibitors of A1 adenosine receptors.

Università
Modulation of A2B adenosine receptor by 1-Benzyl-3-ketoindole derivatives.

University of Pisa
Dual MET and SMO Negative Modulators Overcome Resistance to EGFR Inhibitors in Human Nonsmall Cell Lung Cancer.

University of Campania Luigi Vanvitelli
Hydroxy-substituted amino and ammonium derivatives and their medical use

Gri Bio
Intersubunit bridge formation governs agonist efficacy at nicotinic acetylcholine α4β2 receptors: unique role of halogen bonding revealed.

University of Copenhagen