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| 1 | A2A- adenosine receptor reserve for coronary vasodilation显示文摘 | SHRYOCK JC SNOWDY S BARALDI PG | 1998 | Circulation1998，98，7： | 1 |
| 2 | Ligands for A2B adenosine receptor subtype显示文摘 | Baraldi PG Romagnoli R Preti D | | 0，，： | 1 |
| 3 | Cinnamoyl nitro- gen mustard derivatives of pyrazole analogues of tallimustine modified at the amidino moiety: design, synthesis, molecular modeling and antitumor activity studies显示文摘 | BARALDI PG BERIA l COZZI P | 2004 | Bioorg Med Chem2004，，12： | 1 |
| 4 | Design, synthesis, and biological evaluation of new 8-heterocyclic xanthine derivatives as highly potent and selective human A2B adenosine receptor antagonists 显示文摘 | Baraldi PG Tabrizi MA Preti D | 2004 | J Med Chem2004，47，： | 1 |
| 5 | Cinnamoyl nitrogen mustard derivatives of Pyrazole analogues of tallimustine modified at theamidino moiety: design, synthesis, molecular modeling and antitumor activity studies显示文摘 | Baraldi PG Beria L Cozzi P | 2004 | Bioorg Med Chem2004，12，14： | 1 |
| 6 | Preparation of,4-dihydroxy-1-benzeneethanol:A reinvestigation显示文摘 | BARALDI PG SIMONID MANFREDINI S | 1983 | Liebigs Ann Chem1983，83，： | 1 |
| 7 | A2A-adenosine receptor reserve for coronary vasodilation 显示文摘 | Shryock JC Snowdy S Baraldi PG | 1998 | Circulation1998，98，7： | 1 |
| 8 | A2A-adenosine re- ceptor reserve for coronary vasodilation 显示文摘 | Shryock JC Snowdy S Baraldi PG | 1998 | Circulation1998，98，7： | 1 |
| 9 | Synthe- sis and biological evaluation of 2- and 3 -aminobenzo tlliophene derivatives as antimitotic agents and inhibitors of tubulin polymer- ization显示文摘 | ROMAGNOLI R BARALDI PG CARRION MD | 2007 | J Med Chem2007，50，9： | 1 |
| 10 | Design, synthesis and structure-activity relationship of 2-( 3',4', 5'-trime- thoxybenzoyl)-benzo furan derivatives as a novel class of in- hibitors of tubulin polymerization显示文摘 | ROMAGNOLI R BARALDI PG CARRION MD | 2009 | Bioorg Med Chem2009，17，19： | 1 |
| 11 | Involvement of globus pallidus in the antiparkinsonian effects of adenosine A (2A) receptor antagonists显示文摘 | SIMOLA N FENU S BARALDI PG | 2006 | Exp Neurol2006，202，1： | 1 |
| 12 | Synthe- sis and biological evaluation of 2-amino-3-( 3', 4', 5'-trimethoxy- benzoyl) -6-substituted-4,5,6,7-tetrahydrothieno pyridin e derivatives as antinaitotic agents and inhibitors of tubulin poly- merization 显示文摘 | ROMAGNOLI R BARALDI PG CARRION MD | 2008 | Bioorg Med Chem Lett2008，18，18： | 1 |
| 13 | Cinnamoyl nitrogen mustard derivatives of pyrazole analogues of tallimustine modified at the amidino moiety:design,synthesis,molecular modeling and antitumor activity studies显示文摘 | Baraldi PG Beria I Cozzi P | | 0，，14： | 1 |
| 14 | Synthesis of nitro esters of prednisolone, new compounds combining pharmacological properties of both glucocorticoids and nitric oxide 显示文摘 | Baraldi PG Romagnoli R del Carmen Nunez M | 2004 | J Med Chem2004，47，3： | 1 |
| 15 | Conver- gent synthesis and biological evaluation of 2-amino-4-(3',4',5'- trimethoxyphenyl)-5-aryl thiazoles as microtubule targeting agents 显示文摘 | ROMAGNOLI R BARALDI PG BRANCALE A | 2011 | JMed Chem2011，54，14： | 1 |
| 16 | Substi- tuted 2- ( 3',4', 5'-trimethoxybenzayl) -benzo thiophene deriva- tives as potent tubulin polymerization inhibitors显示文摘 | ROMAGNOLI R BARALDI PG CARRION MD | 2010 | Bioorg Med Chem2010，18，14： | 1 |
| 17 | Design,synthesis and biological activity of a pyrrolobenzodiazepine(PBD)-distamycin hybrid显示文摘 | Baraldi PG Cacciari B Guiotto A | 1998 | Bioorg Med Chem Lett1998，8，21： | 1 |
| 18 | The P2X7 receptor as a therapeutic target显示文摘 | Romagnoli R Baraldi PG Craz-Lopez O Lopez-Cara C Preti D Borea PA | 2008 | Expert Opin Ther Targets2008，12，5： | 1 |
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