Preti D - Search Results

1

N(6)-[(hetero)aryl/(cyclo)alkyl-carbamoyl-methoxy-phenyl]-(2-chloro)-5'-N-ethylcarboxamido-adenosines: the first example of adenosine-related structures with potent agonist activity at the human A(2B) adenosine receptor.

Baraldi PG, Preti D, Tabrizi MA, Fruttarolo F, Saponaro G, Baraldi S, Romagnoli R, Moorman AR, Gessi S, Varani K, Borea PA. Baraldi PG, et al. Among authors: preti d. Bioorg Med Chem. 2007 Apr 1;15(7):2514-27. doi: 10.1016/j.bmc.2007.01.055. Epub 2007 Feb 2. Bioorg Med Chem. 2007. PMID: 17306548

2

Non-neuronal TRPA1 encodes mechanical allodynia associated with neurogenic inflammation and partial nerve injury in rats.

De Logu F, De Siena G, Landini L, Marini M, Souza Monteiro de Araujo D, Albanese V, Preti D, Romitelli A, Chieca M, Titiz M, Iannone LF, Geppetti P, Nassini R. De Logu F, et al. Among authors: preti d. Br J Pharmacol. 2023 May;180(9):1232-1246. doi: 10.1111/bph.16005. Epub 2023 Jan 7. Br J Pharmacol. 2023. PMID: 36494916 Free article.

3

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: preti d. J Med Chem. 2003 Mar 27;46(7):1229-41. doi: 10.1021/jm021023m. J Med Chem. 2003. PMID: 12646033

4

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: preti d. 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

5

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: preti d. Bioorg Med Chem. 2003 Sep 15;11(19):4161-9. doi: 10.1016/s0968-0896(03)00484-x. Bioorg Med Chem. 2003. PMID: 12951147

6

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: preti d. J Med Chem. 2004 Mar 11;47(6):1434-47. doi: 10.1021/jm0309654. J Med Chem. 2004. PMID: 14998332

7

DNA minor groove binders as potential antitumor and antimicrobial agents.

Baraldi PG, Bovero A, Fruttarolo F, Preti D, Tabrizi MA, Pavani MG, Romagnoli R. Baraldi PG, et al. Among authors: preti d. Med Res Rev. 2004 Jul;24(4):475-528. doi: 10.1002/med.20000. Med Res Rev. 2004. PMID: 15170593 Review.

8

[3H]-MRE 2029-F20, a selective antagonist radioligand for the human A2B adenosine receptors.

Baraldi PG, Tabrizi MA, Preti D, Bovero A, Fruttarolo F, Romagnoli R, Moorman AR, Gessi S, Merighi S, Varani K, Borea PA. Baraldi PG, et al. Among authors: preti d. Bioorg Med Chem Lett. 2004 Jul 5;14(13):3607-10. doi: 10.1016/j.bmcl.2004.03.084. Bioorg Med Chem Lett. 2004. PMID: 15177484

9

Synthesis and biological evaluation of novel N6-[4-(substituted)sulfonamidophenylcarbamoyl]adenosine-5'-uronamides as A3 adenosine receptor agonists.

Baraldi PG, Fruttarolo F, Tabrizi MA, Romagnoli R, Preti D, Bovero A, Pineda de Las Infantas MJ, Moorman A, Varani K, Borea PA. Baraldi PG, et al. Among authors: preti d. J Med Chem. 2004 Oct 21;47(22):5535-40. doi: 10.1021/jm0408161. J Med Chem. 2004. PMID: 15481989

10

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: preti d. Farmaco. 2005 Mar;60(3):185-202. doi: 10.1016/j.farmac.2004.09.007. Farmaco. 2005. PMID: 15784237

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