Massa S - Search Results

1

Antifungal agents. 10. New derivatives of 1-[(aryl)[4-aryl-1H-pyrrol-3-yl]methyl]-1H-imidazole, synthesis, anti-candida activity, and quantitative structure-analysis relationship studies.

Tafi A, Costi R, Botta M, Di Santo R, Corelli F, Massa S, Ciacci A, Manetti F, Artico M. Tafi A, et al. Among authors: massa s. J Med Chem. 2002 Jun 20;45(13):2720-32. doi: 10.1021/jm011087h. J Med Chem. 2002. PMID: 12061875

2

3-(1H-Pyrrol-1-yl)-2-oxazolidinones as reversible, highly potent, and selective inhibitors of monoamine oxidase type A.

Mai A, Artico M, Esposito M, Sbardella G, Massa S, Befani O, Turini P, Giovannini V, Mondovì B. Mai A, et al. Among authors: massa s. J Med Chem. 2002 Mar 14;45(6):1180-3. doi: 10.1021/jm015578d. J Med Chem. 2002. PMID: 11881986

3

Design, synthesis and QSAR studies on N-aryl heteroarylisopropanolamines, a new class of non-peptidic HIV-1 protease inhibitors.

Di Santo R, Costi R, Artico M, Massa S, Ragno R, Marshall GR, La Colla P. Di Santo R, et al. Among authors: massa s. Bioorg Med Chem. 2002 Aug;10(8):2511-26. doi: 10.1016/s0968-0896(02)00119-0. Bioorg Med Chem. 2002. PMID: 12057640

4

Computer-aided design, synthesis, and anti-HIV-1 activity in vitro of 2-alkylamino-6-[1-(2,6-difluorophenyl)alkyl]-3,4-dihydro-5-alkylpyrimidin-4(3H)-ones as novel potent non-nucleoside reverse transcriptase inhibitors, also active against the Y181C variant.

Ragno R, Mai A, Sbardella G, Artico M, Massa S, Musiu C, Mura M, Marturana F, Cadeddu A, La Colla P. Ragno R, et al. Among authors: massa s. J Med Chem. 2004 Feb 12;47(4):928-34. doi: 10.1021/jm0309856. J Med Chem. 2004. PMID: 14761194

5

Parallel solution-phase and microwave-assisted synthesis of new S-DABO derivatives endowed with subnanomolar anti-HIV-1 activity.

Manetti F, Esté JA, Clotet-Codina I, Armand-Ugón M, Maga G, Crespan E, Cancio R, Mugnaini C, Bernardini C, Togninelli A, Carmi C, Alongi M, Petricci E, Massa S, Corelli F, Botta M. Manetti F, et al. Among authors: massa s. J Med Chem. 2005 Dec 15;48(25):8000-8. doi: 10.1021/jm050744t. J Med Chem. 2005. PMID: 16335924

6

Toward novel HIV-1 integrase binding inhibitors: molecular modeling, synthesis, and biological studies.

Mugnaini C, Rajamaki S, Tintori C, Corelli F, Massa S, Witvrouw M, Debyser Z, Veljkovic V, Botta M. Mugnaini C, et al. Among authors: massa s. Bioorg Med Chem Lett. 2007 Oct 1;17(19):5370-3. doi: 10.1016/j.bmcl.2007.08.005. Epub 2007 Aug 11. Bioorg Med Chem Lett. 2007. PMID: 17716893

7

Dihydro-alkylthio-benzyl-oxopyrimidines as inhibitors of reverse transcriptase: synthesis and rationalization of the biological data on both wild-type enzyme and relevant clinical mutants.

Mugnaini C, Alongi M, Togninelli A, Gevariya H, Brizzi A, Manetti F, Bernardini C, Angeli L, Tafi A, Bellucci L, Corelli F, Massa S, Maga G, Samuele A, Facchini M, Clotet-Codina I, Armand-Ugón M, Esté JA, Botta M. Mugnaini C, et al. Among authors: massa s. J Med Chem. 2007 Dec 27;50(26):6580-95. doi: 10.1021/jm0708230. Epub 2007 Dec 6. J Med Chem. 2007. PMID: 18052319

8

Antifungal agents. 9. 3-Aryl-4-[alpha-(1H-imidazol-1-yl)arylmethyl]pyrroles: a new class of potent anti-Candida agents.

Artico M, Di Santo R, Costi R, Massa S, Retico A, Artico M, Apuzzo G, Simonetti G, Strippoli V. Artico M, et al. Among authors: massa s. J Med Chem. 1995 Oct 13;38(21):4223-33. doi: 10.1021/jm00021a011. J Med Chem. 1995. PMID: 7473549

9

Antifungal agents. III. Naphthyl and thienyl derivatives of 1H-imidazol-1-yl-4-phenyl-1H-pyrrol-3-ylmethane.

Massa S, Di Santo R, Costi R, Simonetti G, Retico A, Apuzzo G, Artico M. Massa S, et al. Farmaco. 1993 Jun;48(6):725-36. Farmaco. 1993. PMID: 8373500

10

Molecular modeling of azole antifungal agents active against Candida albicans. 1. A comparative molecular field analysis study.

Tafi A, Anastassopoulou J, Theophanides T, Botta M, Corelli F, Massa S, Artico M, Costi R, Di Santo R, Ragno R. Tafi A, et al. Among authors: massa s. J Med Chem. 1996 Mar 15;39(6):1227-35. doi: 10.1021/jm950385+. J Med Chem. 1996. PMID: 8632429

Due to the lack of experimental structural data on these derivatives, molecular mechanics techniques were used to obtain putative active conformations for all the compounds. the correctness of this molecular modeling work was confirmed a posteriori by comparison with structural d …

Due to the lack of experimental structural data on these derivatives, molecular mechanics techniques were used to obtain putative active con …

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