Di Bugno C - Search Results

1

1,2-Cyclomethylenecarboxylic monoamide hydroxamic derivatives. A novel class of non-amino acid angiotensin converting enzyme inhibitors.

Turbanti L, Cerbai G, Di Bugno C, Giorgi R, Garzelli G, Criscuoli M, Renzetti AR, Subissi A, Bramanti G, DePriest SA. Turbanti L, et al. Among authors: di bugno c. J Med Chem. 1993 Mar 19;36(6):699-707. doi: 10.1021/jm00058a006. J Med Chem. 1993. PMID: 8459398

2

1,2-disubstituted cyclohexane derived tripeptide aldehydes as novel selective thrombin inhibitors.

Harmat NJ, Di Bugno C, Criscuoli M, Giorgi R, Lippi A, Martinelli A, Monti S, Subissi A. Harmat NJ, et al. Among authors: di bugno c. Bioorg Med Chem Lett. 1998 May 19;8(10):1249-54. doi: 10.1016/s0960-894x(98)00200-5. Bioorg Med Chem Lett. 1998. PMID: 9871744

3

Absolute configuration and biological activity of mequitamium iodide enantiomers.

Di Bugno C, Dapporto P, Giorgi R, Manzini S, Paoli P, Subissi A, Arcamone F. Di Bugno C, et al. Chirality. 1994;6(5):382-8. doi: 10.1002/chir.530060505. Chirality. 1994. PMID: 8068497

4

Stereoselective inhibition of muscarinic receptor subtypes by the eight stereoisomers related to rociverine.

Barbier P, Renzetti AR, Turbanti L, Di Bugno C, Fornai F, Vaglini F, Maggio R, Corsini GU. Barbier P, et al. Among authors: di bugno c. Eur J Pharmacol. 1995 Jul 18;290(2):125-32. doi: 10.1016/0922-4106(95)90024-1. Eur J Pharmacol. 1995. PMID: 8575526

5

Discovery of potent cyclic pseudopeptide human tachykinin NK-2 receptor antagonists.

Giannotti D, Perrotta E, Di Bugno C, Nannicini R, Harmat NJ, Giolitti A, Patacchini R, Renzetti AR, Rotondaro L, Giuliani S, Altamura M, Maggi CA. Giannotti D, et al. Among authors: di bugno c. J Med Chem. 2000 Nov 2;43(22):4041-4. doi: 10.1021/jm0010217. J Med Chem. 2000. PMID: 11063600 No abstract available.

6

The disaccharide anthracycline MEN 10755 binds human serum albumin to a non-classical drug binding site.

Messori L, Piccioli F, Gabrielli S, Orioli P, Angeloni L, Di Bugno C. Messori L, et al. Among authors: di bugno c. Bioorg Med Chem. 2002 Nov;10(11):3425-30. doi: 10.1016/s0968-0896(02)00265-1. Bioorg Med Chem. 2002. PMID: 12213455

7

Solution chemistry and DNA binding properties of MEN 10755, a novel disaccharide analogue of doxorubicin.

Messori L, Temperini C, Piccioli F, Animati F, Di Bugno C, Orioli P. Messori L, et al. Among authors: di bugno c. Bioorg Med Chem. 2001 Jul;9(7):1815-25. doi: 10.1016/s0968-0896(01)00092-x. Bioorg Med Chem. 2001. PMID: 11425583

8

The crystal structure of the complex between a disaccharide anthracycline and the DNA hexamer d(CGATCG) reveals two different binding sites involving two DNA duplexes.

Temperini C, Messori L, Orioli P, Di Bugno C, Animati F, Ughetto G. Temperini C, et al. Among authors: di bugno c. Nucleic Acids Res. 2003 Mar 1;31(5):1464-9. doi: 10.1093/nar/gkg245. Nucleic Acids Res. 2003. PMID: 12595554 Free PMC article.

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