Angusti A - Search Results

1

Design, synthesis and enzymatic activity of highly selective human mitochondrial thymidine kinase inhibitors.

Manfredini S, Baraldi PG, Durini E, Porcu L, Angusti A, Vertuani S, Solaroli N, De Clercq E, Karlsson A, Balzarini J. Manfredini S, et al. Among authors: angusti a. Bioorg Med Chem Lett. 2001 May 21;11(10):1329-32. doi: 10.1016/s0960-894x(01)00207-4. Bioorg Med Chem Lett. 2001. PMID: 11392548

2

Novel selective human mitochondrial kinase inhibitors: design, synthesis and enzymatic activity.

Ciliberti N, Manfredini S, Angusti A, Durini E, Solaroli N, Vertuani S, Buzzoni L, Bonache MC, Ben-Shalom E, Karlsson A, Saada A, Balzarini J. Ciliberti N, et al. Among authors: angusti a. Bioorg Med Chem. 2007 Apr 15;15(8):3065-81. doi: 10.1016/j.bmc.2007.01.049. Epub 2007 Feb 2. Bioorg Med Chem. 2007. PMID: 17324575

3

Design and synthesis of phosphonoacetic acid (PPA) ester and amide bioisosters of ribofuranosylnucleoside diphosphates as potential ribonucleotide reductase inhibitors and evaluation of their enzyme inhibitory, cytostatic and antiviral activity.

Manfredini S, Solaroli N, Angusti A, Nalin F, Durini E, Vertuani S, Pricl S, Ferrone M, Spadari S, Focher F, Verri A, De Clercq E, Balzarini J. Manfredini S, et al. Among authors: angusti a. Antivir Chem Chemother. 2003 Jul;14(4):183-94. doi: 10.1177/095632020301400403. Antivir Chem Chemother. 2003. PMID: 14582847 Free article.

4

Design, synthesis and anti flaviviridae activity of N(6)-, 5',3'-O- and 5',2'-O-substituted adenine nucleoside analogs.

Angusti A, Manfredini S, Durini E, Ciliberti N, Vertuani S, Solaroli N, Pricl S, Ferrone M, Fermeglia M, Loddo R, Secci B, Visioli A, Sanna T, Collu G, Pezzullo M, La Colla P. Angusti A, et al. Chem Pharm Bull (Tokyo). 2008 Apr;56(4):423-32. doi: 10.1248/cpb.56.423. Chem Pharm Bull (Tokyo). 2008. PMID: 18379085 Free article.

5

The antioxidants and pro-antioxidants network: an overview.

Vertuani S, Angusti A, Manfredini S. Vertuani S, et al. Among authors: angusti a. Curr Pharm Des. 2004;10(14):1677-94. doi: 10.2174/1381612043384655. Curr Pharm Des. 2004. PMID: 15134565 Review.

6

Synthesis and biological evaluation of pro-drugs of GW196771, a potent glycine antagonist acting at the NMDA receptor.

Angusti A, Durini E, Vertuani S, Dalpiaz A, Ruffo A, Di Fabio R, Donati D, Pentassuglia G, Vitulli G, Barnaby RJ, Manfredini S. Angusti A, et al. Farmaco. 2005 May;60(5):393-7. doi: 10.1016/j.farmac.2005.03.007. Farmaco. 2005. PMID: 15885689

7

Adenosine phosphonoacetic acid is slowly metabolized by NDP kinase.

Chen Y, Morera S, Pasti C, Angusti A, Solaroli N, Véron M, Janin J, Manfredini S, Deville-Bonne D. Chen Y, et al. Among authors: angusti a. Med Chem. 2005 Nov;1(6):529-36. doi: 10.2174/157340605774598162. Med Chem. 2005. PMID: 16787337

8

Nanoparticle formulation may affect the stabilization of an antiischemic prodrug.

Leo E, Contado C, Bortolotti F, Pavan B, Scatturin A, Tosi G, Manfredini S, Angusti A, Dalpiaz A. Leo E, et al. Among authors: angusti a. Int J Pharm. 2006 Jan 3;307(1):103-13. doi: 10.1016/j.ijpharm.2005.09.031. Epub 2005 Nov 14. Int J Pharm. 2006. PMID: 16289882

9

Nidogen 1 and 2 gene promoters are aberrantly methylated in human gastrointestinal cancer.

Ulazzi L, Sabbioni S, Miotto E, Veronese A, Angusti A, Gafà R, Manfredini S, Farinati F, Sasaki T, Lanza G, Negrini M. Ulazzi L, et al. Among authors: angusti a. Mol Cancer. 2007 Feb 28;6:17. doi: 10.1186/1476-4598-6-17. Mol Cancer. 2007. PMID: 17328794 Free PMC article.

10

A novel non-antibacterial, non-chelating hydroxypyrazoline derivative of minocycline inhibits nociception and oedema in mice.

Bastos LF, Angusti A, Vilaça MC, Merlo LA, Nascimento EB Jr, Rocha LT, Godin AM, Solano AG, Jarussophon S, Nunan EA, Konishi Y, Coelho MM. Bastos LF, et al. Among authors: angusti a. Br J Pharmacol. 2008 Nov;155(5):714-21. doi: 10.1038/bjp.2008.303. Epub 2008 Jul 28. Br J Pharmacol. 2008. PMID: 18660827 Free PMC article.

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