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Trincavelli Letizia
Trincavelli Maria Letizia
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Maria Letizia
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http://hub.abes.fr/acs/periodical/jmcmar/2000/volume_43/issue_15/101021jm990321p/authorship/10
http://hub.abes.fr/acs/periodical/jmcmar/2002/volume_45/issue_22/101021jm0209580/authorship/15
http://hub.abes.fr/acs/periodical/jmcmar/1998/volume_41/issue_10/101021jm9707737/authorship/4
http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_14/101021jm010827j/authorship/9
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_23/101021jm050407k/authorship/10
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_5/101021jm701240c/authorship/10
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_25/101021jm0504149/authorship/6
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_23/101021jm0708376/authorship/15
http://hub.abes.fr/acs/periodical/jmcmar/2002/volume_45/issue_23/101021jm020911e/authorship/12
http://hub.abes.fr/acs/periodical/jmcmar/2004/volume_47/issue_14/101021jm031136l/authorship/8
http://hub.abes.fr/acs/periodical/jmcmar/2006/volume_49/issue_13/101021jm060373w/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/2000/volume_43/issue_16/101021jm000936i/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/2000/volume_43/issue_6/101021jm991096e/authorship/7
http://hub.abes.fr/acs/periodical/jmcmar/2008/volume_51/issue_6/101021jm701159t/authorship/12
http://hub.abes.fr/acs/periodical/jmcmar/2007/volume_50/issue_17/101021jm070123v/authorship/8
http://hub.abes.fr/acs/periodical/jmcmar/2005/volume_48/issue_26/101021jm050792d/authorship/16
http://hub.abes.fr/acs/periodical/jmcmar/2000/volume_43/issue_1/101021jm991131h/authorship/9
http://hub.abes.fr/acs/periodical/jmcmar/2001/volume_44/issue_3/101021jm001054m/authorship/9
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Synthesis and Structure−Activity Relationships of a New Set of2-Arylpyrazolo[3,4-c]quinoline Derivatives as Adenosine Receptor Antagonists
2‘-C-Methyl Analogues of Selective Adenosine Receptor Agonists: Synthesis andBinding Studies
5-Amino-2-phenyl[1,2,3]triazolo[1,2-a][1,2,4]benzotriazin-1-one: A Versatile Scaffold To ObtainPotent and Selective A3 Adenosine Receptor Antagonists
3-Aryl-[1,2,4]triazino[4,3-a]benzimidazol-4(10H)-ones: Tricyclic HeteroaromaticDerivatives as a New Class of Benzodiazepine Receptor Ligands
1,2,4-Triazolo[1,5-a]quinoxaline as a Versatile Tool for the Design of SelectiveHuman A3 Adenosine Receptor Antagonists: Synthesis, Biological Evaluation,and Molecular Modeling Studies of 2-(Hetero)aryl- and 2-Carboxy-SubstituedDerivatives
A Novel Class of Highly Potent and Selective A1 Adenosine Antagonists: Structure−Affinity Profile of a Series of 1,8-Naphthyridine Derivatives
4-Amido-2-aryl-1,2,4-triazolo[4,3-a]quinoxalin-1-ones as New Potent and Selective Human A3Adenosine Receptor Antagonists. Synthesis, Pharmacological Evaluation, and Ligand−ReceptorModeling Studies
1,2,4-Triazolo[4,3-a]quinoxalin-1-one: A Versatile Tool for the Synthesis ofPotent and Selective Adenosine Receptor Antagonists
Novel N-(Arylalkyl)indol-3-ylglyoxylylamides Targeted as Ligands of theBenzodiazepine Receptor: Synthesis, Biological Evaluation, and MolecularModeling Analysis of the Structure−Activity Relationships
Synthesis, Molecular Modeling Studies, and Pharmacological Activity ofSelective A1 Receptor Antagonists
Derivatives of 4-Amino-6-hydroxy-2-mercaptopyrimidine as Novel, Potent, and Selective A3 Adenosine Receptor Antagonists
Synthesis and 3D QSAR of New Pyrazolo[3,4-b]pyridines: Potent and SelectiveInhibitors of A1 Adenosine Receptors
2-(Benzimidazol-2-yl)quinoxalines: A Novel Class of Selective Antagonists atHuman A1 and A3 Adenosine Receptors Designed by 3D Database Searching
New 2-Arylpyrazolo[3,4-c]quinoline Derivatives as Potent and Selective Human A3 AdenosineReceptor Antagonists. Synthesis, Pharmacological Evaluation, and Ligand−ReceptorModeling Studies
1,2,4-Triazolo[4,3-a]quinoxalin-1-one Moiety as an Attractive Scaffold ToDevelop New Potent and Selective Human A3 Adenosine Receptor Antagonists: Synthesis, Pharmacological, and Ligand−Receptor Modeling Studies
3-Aryl[1,2,4]triazino[4,3-a]benzimidazol-4(10H)-ones: A New Class of SelectiveA1 Adenosine Receptor Antagonists
Design, Synthesis and Biological Evaluation of Novel N-Alkyl- andN-Acyl-(7-substituted-2-phenylimidazo[1,2-a][1,3,5]triazin-4-yl)amines (ITAs) asNovel A1 Adenosine Receptor Antagonists
Structure-Based Optimization of Pyrazolo[3,4-d]pyrimidines as Abl Inhibitors and Antiproliferative Agents toward Human Leukemia Cell Lines
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