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机译:1,2,4-三唑并4,3-a喹喔啉-1-酮部分作为有吸引力的支架开发新的强效和选择性人A_3腺苷受体拮抗剂:合成、药理学和配体受体建模研究
Dipartimento di Scienze Farmaceutiche, Universita degli Studi di Firenze, Polo Scientifico, Via Ugo Schiff, 6, 50019 Sesto Fiorentino (FI), Italy;
Dipartimento di Psichiatria, Neurobiologia, Farmacologia e Biotecnologie, Universita degli Studi di Pisa, Via Bonanno, 6, 50126 Pisa, Italy;
Molecular Modeling Section, Dipartimento di Scienze Farmaceutiche, Universita degli Studi di Padova, Via Marzolo, 5, 35131 Padova, Italy;
机译:Synthesis, ligand-receptor modeling studies and pharmacological evaluation of novel 4-modified-2-aryl-1,2,4-triazolo(4,3-a)quinoxalin-1-one derivatives as potent and selective human A3 adenosine receptor antagonists.
机译:Synthesis of 4-amino-6-(hetero)arylalkylamino-1,2,4-triazolo(4,3-a)quinoxalin-1-one derivatives as potent A(2A) adenosine receptor antagonists.
机译:Synthesis and structure-activity relationships of a new set of 1,2,4-triazolo(4,3-a)quinoxalin-1-one derivatives as adenosine receptor antagonists.