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| 1 | 6-Amino-4-oxo-1,3-diphenyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonyl derivatives as a new class of potent inhibitors of interleukin-8-induced neutrophil chemotaxis显示文摘 | Cesarini S Spallarossa A Ranise A | 2009 | Bioorg Med Chem2009，17，10： | 1 |
| 2 | Economics Growth and Human Development 显示文摘 | Ranis Gustav F Stewart A Ramirez | 2000 | World Development2000，28，2： | 1 |
| 3 | Structure-Based Design, Parallel Synthesis, Structure-Activity Relationship,and Molecular Modeling Studies of Thiocarbamates, New Potent Non-Nucleoside HIV-1 Reverse Transcriptase Inhibitor Isosteres of Phenethyhhiazolyhhiourea Derivatives 显示文摘 | Ranise A Spallarossa A Cesarini S | 2005 | J Med Chem2005，48，： | 1 |
| 4 | Synthesis N- substituted-N-acyhhioureas of d-substituted piperazines endowed with local anaesthetic, antihyperlipidemic, antiproliferative activities and antiarrythmic, analgesic, antiaggregating actions 显示文摘 | Ranise A Spallarossa A Bruno O | 2003 | I1 Farmaco2003，58，： | 1 |
| 5 | 6-amino-4-oxo-1,3-diphenyl-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonyl derivatives as a new class of potent inhibitors of Interleukin-8-induced neutrophil chemotaxis显示文摘 | Cesarini S Spallarossa A Ranise A | | 0，，10： | 1 |
| 6 | New pyrazolo pyrimidines endowed with A431antiproliferative activity and inhibitory properties of Src phosphorylation显示文摘 | SCHENONE S BRUNO O RANISE A | 2004 | Bioorg Med Chem Lett2004，14，10： | 1 |
| 7 | New pyrazolo pyrimidines endowed with A431 antiproliferative activity and inhibitory properties of Src phosphorylation显示文摘 | SCHENONE S BRUNO O RANISE A | 2004 | Bioorg Med Chem Lett2004，14，10： | 1 |
| 8 | 6-amino- 4-oxo-1,3-diphenyl-2-thioxo- 1,2,3,4-tetrahydropyrimidine-5-carbonyl derivatives as a new class of potent inhibitors of Interleukin-8-induced neutrophil chemotaxis 显示文摘 | CESARINI S SPALLAROSSA A RANISE A | 2009 | Bioorg Med Chem2009，17，10： | 1 |
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