1,2,4-Triazolo[1,5-a]quinoxaline as a versatile tool for the design of selective human A3 adenosine receptor antagonists: synthesis, biological evaluation, and molecular modeling studies of 2-(hetero)aryl- and 2-carboxy-substituted derivatives.
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S. Moro | C. Martini | L. Trincavelli | Ombretta Lenzi | D. Catarzi | V. Colotta | G. Filacchioni | F. Varano | C. Montopoli