Pregnolato M - Search Results

1

Potentiation of inhibition of wild-type and mutant human immunodeficiency virus type 1 reverse transcriptases by combinations of nonnucleoside inhibitors and d- and L-(beta)-dideoxynucleoside triphosphate analogs.

Maga G, Hübscher U, Pregnolato M, Ubiali D, Gosselin G, Spadari S. Maga G, et al. Among authors: pregnolato m. Antimicrob Agents Chemother. 2001 Apr;45(4):1192-200. doi: 10.1128/AAC.45.4.1192-1200.2001. Antimicrob Agents Chemother. 2001. PMID: 11257034 Free PMC article.

2

Selective interaction of the human immunodeficiency virus type 1 reverse transcriptase nonnucleoside inhibitor efavirenz and its thio-substituted analog with different enzyme-substrate complexes.

Maga G, Ubiali D, Salvetti R, Pregnolato M, Spadari S. Maga G, et al. Among authors: pregnolato m. Antimicrob Agents Chemother. 2000 May;44(5):1186-94. doi: 10.1128/AAC.44.5.1186-1194.2000. Antimicrob Agents Chemother. 2000. PMID: 10770750 Free PMC article.

3

Novel nonsubstrate inhibitors of human thymidine phosphorylase, a potential target for tumor-dependent angiogenesis.

Focher F, Ubiali D, Pregnolato M, Zhi C, Gambino J, Wright GE, Spadari S. Focher F, et al. Among authors: pregnolato m. J Med Chem. 2000 Jun 29;43(13):2601-7. doi: 10.1021/jm000037u. J Med Chem. 2000. PMID: 10891120

4

5-(Trifluoromethyl)-beta-l-2'-deoxyuridine, the L-enantiomer of trifluorothymidine: stereospecific synthesis and antiherpetic evaluations.

Salvetti R, Marchand A, Pregnolato M, Verri A, Spadari S, Focher F, Briant M, Sommadossi JP, Mathé C, Gosselin G. Salvetti R, et al. Among authors: pregnolato m. Bioorg Med Chem. 2001 Jul;9(7):1731-8. doi: 10.1016/s0968-0896(01)00062-1. Bioorg Med Chem. 2001. PMID: 11425574

5

Synthesis and in vitro activity of D- and L-enantiomers of 5-(trifluoromethyl)uracil nucleoside derivatives.

Salvetti R, Pregnolato M, Verri A, Focher F, Spadari S, Marchand A, Mathé C, Gosselin G. Salvetti R, et al. Among authors: pregnolato m. Nucleosides Nucleotides Nucleic Acids. 2001 Apr-Jul;20(4-7):1123-5. doi: 10.1081/NCN-100002502. Nucleosides Nucleotides Nucleic Acids. 2001. PMID: 11562969

6

Synthesis and molecular modeling of novel HSV1 uracil-DNA glycosylase inhibitors.

Pregnolato M, Ubiali D, Verri A, Focher F, Spadari S, Sun H, Zhi C, Wright GE. Pregnolato M, et al. Nucleosides Nucleotides. 1999 Apr-May;18(4-5):709-11. doi: 10.1080/15257779908041549. Nucleosides Nucleotides. 1999. PMID: 10432670

7

Synthesis and in vitro anti-mycobacterium activity of N-alkyl-1, 2-dihydro-2-thioxo-3-pyridinecarbothioamides. Preliminary toxicity and pharmacokinetic evaluation.

Pagani G, Pregnolato M, Ubiali D, Terreni M, Piersimoni C, Scaglione F, Fraschini F, Gascón AR, Pedraz Muñoz JL. Pagani G, et al. Among authors: pregnolato m. J Med Chem. 2000 Jan 27;43(2):199-204. doi: 10.1021/jm991044p. J Med Chem. 2000. PMID: 10649975

8

3H-[1,2]Dithiolo[3,4-b]pyridine-3-thione and its derivatives synthesis and antimicrobial activity.

Pregnolato M, Terreni M, Ubiali D, Pagani G, Borgna P, Pastoni F, Zampollo F. Pregnolato M, et al. Farmaco. 2000 Nov-Dec;55(11-12):669-79. doi: 10.1016/s0014-827x(00)00084-7. Farmaco. 2000. PMID: 11204941

9

Molecular modeling and synthesis of inhibitors of herpes simplex virus type 1 uracil-DNA glycosylase.

Sun H, Zhi C, Wright GE, Ubiali D, Pregnolato M, Verri A, Focher F, Spadari S. Sun H, et al. Among authors: pregnolato m. J Med Chem. 1999 Jul 1;42(13):2344-50. doi: 10.1021/jm980718d. J Med Chem. 1999. PMID: 10395474

10

New N-alkyl-1,2-dihydro-2-thioxo-3-pyridinecarbothioamides as antituberculous agents with improved pharmacokinetics.

Ubiali D, Pagani G, Pregnolato M, Piersimoni C, Pedraz Muñoz JL, Rodríguez Gascón A, Terreni M. Ubiali D, et al. Among authors: pregnolato m. Bioorg Med Chem Lett. 2002 Sep 16;12(18):2541-4. doi: 10.1016/s0960-894x(02)00490-0. Bioorg Med Chem Lett. 2002. PMID: 12182855

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