Franchetti P - Search Results

1

Synthesis and evaluation of the anti-HIV activity of aza and deaza analogues of isoddA and their phosphates as prodrugs.

Franchetti P, Cappellacci L, Grifantini M, Messini L, abu Sheikha G, Loi AG, Tramontano E, de Montis A, Spiga MG, La Colla P. Franchetti P, et al. J Med Chem. 1994 Oct 14;37(21):3534-41. doi: 10.1021/jm00047a011. J Med Chem. 1994. PMID: 7523675

2

Ribose-modified nucleosides as ligands for adenosine receptors: synthesis, conformational analysis, and biological evaluation of 1'-C-methyl adenosine analogues.

Cappellacci L, Barboni G, Palmieri M, Pasqualini M, Grifantini M, Costa B, Martini C, Franchetti P. Cappellacci L, et al. Among authors: franchetti p. J Med Chem. 2002 Mar 14;45(6):1196-202. doi: 10.1021/jm0102755. J Med Chem. 2002. PMID: 11881988

3

Synthesis, biological evaluation, and molecular modeling of ribose-modified adenosine analogues as adenosine receptor agonists.

Cappellacci L, Franchetti P, Pasqualini M, Petrelli R, Vita P, Lavecchia A, Novellino E, Costa B, Martini C, Klotz KN, Grifantini M. Cappellacci L, et al. Among authors: franchetti p. J Med Chem. 2005 Mar 10;48(5):1550-62. doi: 10.1021/jm049408n. J Med Chem. 2005. PMID: 15743197

4

Antitumor activity of C-methyl-beta-D-ribofuranosyladenine nucleoside ribonucleotide reductase inhibitors.

Franchetti P, Cappellacci L, Pasqualini M, Petrelli R, Vita P, Jayaram HN, Horvath Z, Szekeres T, Grifantini M. Franchetti P, et al. J Med Chem. 2005 Jul 28;48(15):4983-9. doi: 10.1021/jm048944c. J Med Chem. 2005. PMID: 16033277

5

Ribose-modified purine nucleosides as ribonucleotide reductase inhibitors. Synthesis, antitumor activity, and molecular modeling of N6-substituted 3'-C-methyladenosine derivatives.

Cappellacci L, Franchetti P, Vita P, Petrelli R, Lavecchia A, Jayaram HN, Saiko P, Graser G, Szekeres T, Grifantini M. Cappellacci L, et al. Among authors: franchetti p. J Med Chem. 2008 Jul 24;51(14):4260-9. doi: 10.1021/jm800205c. Epub 2008 Jun 28. J Med Chem. 2008. PMID: 18588281

6

Adenosine deaminase inhibitors: synthesis and structure-activity relationships of imidazole analogues of erythro-9-(2-hydroxy-3-nonyl)adenine.

Cristalli G, Eleuteri A, Franchetti P, Grifantini M, Vittori S, Lupidi G. Cristalli G, et al. Among authors: franchetti p. J Med Chem. 1991 Mar;34(3):1187-92. doi: 10.1021/jm00107a044. J Med Chem. 1991. PMID: 2002459

7

Synthesis and antitumor activity of 2-beta-D-ribofuranosyloxazole-4-carboxamide (oxazofurin).

Franchetti P, Cristalli G, Grifantini M, Cappellacci L, Vittori S, Nocentini G. Franchetti P, et al. J Med Chem. 1990 Oct;33(10):2849-52. doi: 10.1021/jm00172a027. J Med Chem. 1990. PMID: 2120442

8

Adenosine deaminase inhibitors. Synthesis and biological activity of deaza analogues of erythro-9-(2-hydroxy-3-nonyl)adenine.

Cristalli G, Franchetti P, Grifantini M, Vittori S, Lupidi G, Riva F, Bordoni T, Geroni C, Verini MA. Cristalli G, et al. Among authors: franchetti p. J Med Chem. 1988 Feb;31(2):390-3. doi: 10.1021/jm00397a021. J Med Chem. 1988. PMID: 3339608

9

Adenosine receptor agonists: synthesis and biological evaluation of 1-deaza analogues of adenosine derivatives.

Cristalli G, Franchetti P, Grifantini M, Vittori S, Klotz KN, Lohse MJ. Cristalli G, et al. Among authors: franchetti p. J Med Chem. 1988 Jun;31(6):1179-83. doi: 10.1021/jm00401a018. J Med Chem. 1988. PMID: 3373486

10

Furanfurin and thiophenfurin: two novel tiazofurin analogues. Synthesis, structure, antitumor activity, and interactions with inosine monophosphate dehydrogenase.

Franchetti P, Cappellacci L, Grifantini M, Barzi A, Nocentini G, Yang H, O'Connor A, Jayaram HN, Carrell C, Goldstein BM. Franchetti P, et al. J Med Chem. 1995 Sep 15;38(19):3829-37. doi: 10.1021/jm00019a013. J Med Chem. 1995. PMID: 7562914

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