Artico M - Search Results

1

Computer-assisted design, synthesis and biological evaluation of novel pyrrolyl heteroaryl sulfones targeted at HIV-1 reverse transcriptase as non-nucleoside inhibitors.

Silvestri R, Artico M, De Martino G, Novellino E, Greco G, Lavecchia A, Massa S, Loi AG, Doratiotto S, La Colla P. Silvestri R, et al. Among authors: artico m. Bioorg Med Chem. 2000 Sep;8(9):2305-9. doi: 10.1016/s0968-0896(00)00144-9. Bioorg Med Chem. 2000. PMID: 11026542

2

Characterization of the anti-HIV-1 activity of 3,4-dihydro-2-alkoxy-6-benzyl-4-oxopyrimidines (DABOs), new non-nucleoside reverse transcriptase inhibitors.

Tramontano E, Marongiu ME, de Montis A, Loi AG, Artico M, Massa S, Mai A, la Colla P. Tramontano E, et al. Among authors: artico m. New Microbiol. 1994 Oct;17(4):269-79. New Microbiol. 1994. PMID: 7532270

3

Synthesis of pyrryl aryl sulfones targeted at the HIV-1 reverse transcriptase.

Artico M, Silvestri R, Stefancich G, Massa S, Pagnozzi E, Musu D, Scintu F, Pinna E, Tinti E, La Colla P. Artico M, et al. Arch Pharm (Weinheim). 1995 Mar;328(3):223-9. doi: 10.1002/ardp.19953280304. Arch Pharm (Weinheim). 1995. PMID: 7539250

4

Synthesis and anti-HIV-1 activity of thio analogues of dihydroalkoxybenzyloxopyrimidines.

Mai A, Artico M, Sbardella G, Massa S, Loi AG, Tramontano E, Scano P, La Colla P. Mai A, et al. Among authors: artico m. J Med Chem. 1995 Aug 18;38(17):3258-63. doi: 10.1021/jm00017a010. J Med Chem. 1995. PMID: 7650679

5

2-Sulfonyl-4-chloroanilino moiety: a potent pharmacophore for the anti-human immunodeficiency virus type 1 activity of pyrrolyl aryl sulfones.

Artico M, Silvestri R, Massa S, Loi AG, Corrias S, Piras G, La Colla P. Artico M, et al. J Med Chem. 1996 Jan 19;39(2):522-30. doi: 10.1021/jm950568w. J Med Chem. 1996. PMID: 8558522

6

5H-pyrrolo[1,2-b] [1,2,5]benzothiadiazepines (PBTDs): a novel class of non-nucleoside reverse transcriptase inhibitors.

Artico M, Silvestri R, Pagnozzi E, Stefancich G, Massa S, Loi AG, Putzolu M, Corrias S, Spiga MG, La Colla P. Artico M, et al. Bioorg Med Chem. 1996 Jun;4(6):837-50. doi: 10.1016/0968-0896(96)00075-2. Bioorg Med Chem. 1996. PMID: 8818233

7

Dihydro(alkylthio)(naphthylmethyl)oxopyrimidines: novel non-nucleoside reverse transcriptase inhibitors of the S-DABO series.

Mai A, Artico M, Sbardella G, Quartarone S, Massa S, Loi AG, De Montis A, Scintu F, Putzolu M, La Colla P. Mai A, et al. Among authors: artico m. J Med Chem. 1997 May 9;40(10):1447-54. doi: 10.1021/jm960802y. J Med Chem. 1997. PMID: 9154967

8

Sulfone derivatives with anti-HIV activity.

Silvestri R, Artico M, Massa S, Stefancich G, Congeddu E, Putzolu M, La Colla P. Silvestri R, et al. Among authors: artico m. Farmaco. 1997 May;52(5):323-9. Farmaco. 1997. PMID: 9274003

9

Geometrically and conformationally restrained cinnamoyl compounds as inhibitors of HIV-1 integrase: synthesis, biological evaluation, and molecular modeling.

Artico M, Di Santo R, Costi R, Novellino E, Greco G, Massa S, Tramontano E, Marongiu ME, De Montis A, La Colla P. Artico M, et al. J Med Chem. 1998 Oct 8;41(21):3948-60. doi: 10.1021/jm9707232. J Med Chem. 1998. PMID: 9767632

10

Synthesis and biological evaluation of 5H-indolo [3,2-b][1,5]benzothiazepine derivatives, designed as conformationally constrained analogues of the human immunodeficiency virus type 1 reverse transcriptase inhibitor L-737,126.

Silvestri R, Artico M, Bruno B, Massa S, Novellino E, Greco G, Marongiu ME, Pani A, De Montis A, La Colla P. Silvestri R, et al. Among authors: artico m. Antivir Chem Chemother. 1998 Mar;9(2):139-48. doi: 10.1177/095632029800900205. Antivir Chem Chemother. 1998. PMID: 9875385

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