Fruttarolo F - Search Results

1

New heterocyclic ligands for the adenosine receptors P1 and for the ATP receptors P2.

Baraldi PG, Romagnoli R, Tabrizi MA, Bovero A, Preti D, Fruttarolo F, Moorman AR, Borea PA. Baraldi PG, et al. Among authors: fruttarolo f. Farmaco. 2005 Mar;60(3):185-202. doi: 10.1016/j.farmac.2004.09.007. Farmaco. 2005. PMID: 15784237

2

Design, synthesis, and biological evaluation of C9- and C2-substituted pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidines as new A2A and A3 adenosine receptors antagonists.

Baraldi PG, Fruttarolo F, Tabrizi MA, Preti D, Romagnoli R, El-Kashef H, Moorman A, Varani K, Gessi S, Merighi S, Borea PA. Baraldi PG, et al. Among authors: fruttarolo f. J Med Chem. 2003 Mar 27;46(7):1229-41. doi: 10.1021/jm021023m. J Med Chem. 2003. PMID: 12646033

3

Recent developments in the field of A2A and A3 adenosine receptor antagonists.

Baraldi PG, Tabrizi MA, Bovero A, Avitabile B, Preti D, Fruttarolo F, Romagnoli R, Varani K, Borea PA. Baraldi PG, et al. Among authors: fruttarolo f. Eur J Med Chem. 2003 Apr;38(4):367-82. doi: 10.1016/s0223-5234(03)00042-4. Eur J Med Chem. 2003. PMID: 12750024

4

New strategies for the synthesis of A3 adenosine receptor antagonists.

Baraldi PG, Bovero A, Fruttarolo F, Romagnoli R, Tabrizi MA, Preti D, Varani K, Borea PA, Moorman AR. Baraldi PG, et al. Among authors: fruttarolo f. Bioorg Med Chem. 2003 Sep 15;11(19):4161-9. doi: 10.1016/s0968-0896(03)00484-x. Bioorg Med Chem. 2003. PMID: 12951147

5

Design, synthesis, and biological evaluation of new 8-heterocyclic xanthine derivatives as highly potent and selective human A2B adenosine receptor antagonists.

Baraldi PG, Tabrizi MA, Preti D, Bovero A, Romagnoli R, Fruttarolo F, Zaid NA, Moorman AR, Varani K, Gessi S, Merighi S, Borea PA. Baraldi PG, et al. Among authors: fruttarolo f. J Med Chem. 2004 Mar 11;47(6):1434-47. doi: 10.1021/jm0309654. J Med Chem. 2004. PMID: 14998332

6

Pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidine ligands, new tools to characterize A3 adenosine receptors in human tumor cell lines.

Baraldi PG, Tabrizi MA, Romagnoli R, Fruttarolo F, Merighi S, Varani K, Gessi S, Borea PA. Baraldi PG, et al. Among authors: fruttarolo f. Curr Med Chem. 2005;12(11):1319-29. doi: 10.2174/0929867054020963. Curr Med Chem. 2005. PMID: 15974999 Review.

7

New pyrrolo[2,1-f]purine-2,4-dione and imidazo[2,1-f]purine-2,4-dione derivatives as potent and selective human A3 adenosine receptor antagonists.

Baraldi PG, Preti D, Tabrizi MA, Fruttarolo F, Romagnoli R, Zaid NA, Moorman AR, Merighi S, Varani K, Borea PA. Baraldi PG, et al. Among authors: fruttarolo f. J Med Chem. 2005 Jul 14;48(14):4697-701. doi: 10.1021/jm058008c. J Med Chem. 2005. PMID: 16000006

8

New 2-arylpyrazolo[4,3-c]quinoline derivatives as potent and selective human A3 adenosine receptor antagonists.

Baraldi PG, Tabrizi MA, Preti D, Bovero A, Fruttarolo F, Romagnoli R, Zaid NA, Moorman AR, Varani K, Borea PA. Baraldi PG, et al. Among authors: fruttarolo f. J Med Chem. 2005 Jul 28;48(15):5001-8. doi: 10.1021/jm050125k. J Med Chem. 2005. PMID: 16033279

9

Ligands for A2B adenosine receptor subtype.

Baraldi PG, Romagnoli R, Preti D, Fruttarolo F, Carrion MD, Tabrizi MA. Baraldi PG, et al. Among authors: fruttarolo f. Curr Med Chem. 2006;13(28):3467-82. doi: 10.2174/092986706779010306. Curr Med Chem. 2006. PMID: 17168717 Review.

10

Pyrazolo-triazolo-pyrimidine derivatives as adenosine receptor antagonists: a possible template for adenosine receptor subtypes?

Baraldi PG, Cacciari B, Borean PA, Varanin K, Pastorin G, Da Ros T, Tabrizi MA, Fruttarolo F, Spalluto G. Baraldi PG, et al. Among authors: fruttarolo f. Curr Pharm Des. 2002;8(26):2299-332. doi: 10.2174/1381612023392838. Curr Pharm Des. 2002. PMID: 12369947 Review.

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