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13 articles for ML Trincavelli


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
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.EBI
Universita Degli Studi Di Firenze
Combining galantamine and memantine in multitargeted, new chemical entities potentially useful in Alzheimer's disease.EBI
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.EBI
University of Pisa
Novel N2-substituted pyrazolo[3,4-d]pyrimidine adenosine A3 receptor antagonists: inhibition of A3-mediated human glioblastoma cell proliferation.EBI
University of Pisa
Structure-based optimization of pyrazolo[3,4-d]pyrimidines as Abl inhibitors and antiproliferative agents toward human leukemia cell lines.EBI
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.EBI
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.EBI
University of Naples Federico II
Frontal affinity chromatography-mass spectrometry useful for characterization of new ligands for GPR17 receptor.EBI
University of Pavia
Synthesis and 3D QSAR of new pyrazolo[3,4-b]pyridines: potent and selective inhibitors of A1 adenosine receptors.EBI
Università
Modulation of A2B adenosine receptor by 1-Benzyl-3-ketoindole derivatives.EBI
University of Pisa
Dual MET and SMO Negative Modulators Overcome Resistance to EGFR Inhibitors in Human Nonsmall Cell Lung Cancer.EBI
University of Campania Luigi Vanvitelli
Hydroxy-substituted amino and ammonium derivatives and their medical useBDB
Gri Bio
Intersubunit bridge formation governs agonist efficacy at nicotinic acetylcholine α4β2 receptors: unique role of halogen bonding revealed.BDB
University of Copenhagen