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DESIGN, SYNTHESIS, AND BIOLOGICAL EVALUATION OF A 2ND-GENERATION OF PYRAZOLO[4,3-E]-1,2,4-TRIAZOLO[1,5-C]PYRIMIDINES AS POTENT AND SELECTIVE A(2A) ADENOSINE RECEPTOR ANTAGONISTS
Authors: BARALDI PG CACCIARI B SPALLUTO G BERGONZONI M DIONISOTTI S ONGINI E VARANI K BOREA PA
Citation: Pg. Baraldi et al., DESIGN, SYNTHESIS, AND BIOLOGICAL EVALUATION OF A 2ND-GENERATION OF PYRAZOLO[4,3-E]-1,2,4-TRIAZOLO[1,5-C]PYRIMIDINES AS POTENT AND SELECTIVE A(2A) ADENOSINE RECEPTOR ANTAGONISTS, Journal of medicinal chemistry, 41(12), 1998, pp. 2126-2133
SYMMETRY-BASED HIV PROTEASE INHIBITORS CONTAINING (S,S) OR (R,R) TARTARIC ACID CORE STRUCTURE
Authors: MARASTONI M BERGONZONI M BORTOLOTTI F TOMATIS R
Citation: M. Marastoni et al., SYMMETRY-BASED HIV PROTEASE INHIBITORS CONTAINING (S,S) OR (R,R) TARTARIC ACID CORE STRUCTURE, Arzneimittel-Forschung, 47(7), 1997, pp. 889-892
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