Mai A - Search Results

1

Pure enantiomers of benzoylamino-tranylcypromine: LSD1 inhibition, gene modulation in human leukemia cells and effects on clonogenic potential of murine promyelocytic blasts.

Valente S, Rodriguez V, Mercurio C, Vianello P, Saponara B, Cirilli R, Ciossani G, Labella D, Marrocco B, Monaldi D, Ruoppolo G, Tilset M, Botrugno OA, Dessanti P, Minucci S, Mattevi A, Varasi M, Mai A. Valente S, et al. Among authors: mai a. Eur J Med Chem. 2015 Apr 13;94:163-74. doi: 10.1016/j.ejmech.2015.02.060. Epub 2015 Mar 3. Eur J Med Chem. 2015. PMID: 25768700

2

Pyrrolobenzodiazepines and related systems. 2. Synthesis and biological properties of isonoraptazepine derivatives.

Massa S, Artico M, Mai A, Corelli F, Botta M, Tafi A, Pantaleoni GC, Giorgi R, Coppolino MF, Cagnotto A, et al. Massa S, et al. Among authors: mai a. J Med Chem. 1992 Nov 27;35(24):4533-41. doi: 10.1021/jm00102a004. J Med Chem. 1992. PMID: 1335075

3

Synthesis and antimicrobial and cytotoxic activities of pyrrole-containing analogues of trichostatin A.

Massa S, Artico M, Corelli F, Mai A, Di Santo R, Cortes S, Marongiu ME, Pani A, La Colla P. Massa S, et al. Among authors: mai a. J Med Chem. 1990 Oct;33(10):2845-9. doi: 10.1021/jm00172a026. J Med Chem. 1990. PMID: 2213836

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. J Med Chem. 1995 Aug 18;38(17):3258-63. doi: 10.1021/jm00017a010. J Med Chem. 1995. PMID: 7650679

5

[[[(Thienylcarbonyl)alkyl]oxy]phenyl]- and [[[(pyrrylcarbonyl)alkyl]oxy]phenyl]oxazoline derivatives with potent and selective antihuman rhinovirus activity.

Massa S, Corelli F, Artico M, Mai A, Ragno R, De Montis A, Loi AG, Corrias S, Marongiu ME, La Colla P. Massa S, et al. Among authors: mai a. J Med Chem. 1995 Mar 3;38(5):803-9. doi: 10.1021/jm00005a007. J Med Chem. 1995. PMID: 7877145

6

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. J Med Chem. 1997 May 9;40(10):1447-54. doi: 10.1021/jm960802y. J Med Chem. 1997. PMID: 9154967

7

5-Alkyl-2-(alkylthio)-6-(2,6-dihalophenylmethyl)-3, 4-dihydropyrimidin-4(3H)-ones: novel potent and selective dihydro-alkoxy-benzyl-oxopyrimidine derivatives.

Mai A, Artico M, Sbardella G, Massa S, Novellino E, Greco G, Loi AG, Tramontano E, Marongiu ME, La Colla P. Mai A, et al. J Med Chem. 1999 Feb 25;42(4):619-27. doi: 10.1021/jm980260f. J Med Chem. 1999. PMID: 10052969

8

Structure-based design, synthesis, and biological evaluation of conformationally restricted novel 2-alkylthio-6-[1-(2,6-difluorophenyl)alkyl]-3,4-dihydro-5-alkylpyrimidin-4(3H)-ones as non-nucleoside inhibitors of HIV-1 reverse transcriptase.

Mai A, Sbardella G, Artico M, Ragno R, Massa S, Novellino E, Greco G, Lavecchia A, Musiu C, La Colla M, Murgioni C, La Colla P, Loddo R. Mai A, et al. J Med Chem. 2001 Aug 2;44(16):2544-54. doi: 10.1021/jm010853h. J Med Chem. 2001. PMID: 11472208

5-Alkyl-2-(alkylthio)-6-(2,6-difluorobenzyl)-3,4-dihydropyrimidin-4(3H)-ones (S-DABOs, 2) have been recently described as a new class of human immunodeficiency virus type 1 (HIV-1) non-nucleoside reverse transcriptase (RT) inhibitors (NNRTIs) active at nanomolar concentrat …

5-Alkyl-2-(alkylthio)-6-(2,6-difluorobenzyl)-3,4-dihydropyrimidin-4(3H)-ones (S-DABOs, 2) have been recently described as a new class …

9

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. J Med Chem. 2002 Mar 14;45(6):1180-3. doi: 10.1021/jm015578d. J Med Chem. 2002. PMID: 11881986

10

Binding mode analysis of 3-(4-benzoyl-1-methyl-1H-2-pyrrolyl)-N-hydroxy-2-propenamide: a new synthetic histone deacetylase inhibitor inducing histone hyperacetylation, growth inhibition, and terminal cell differentiation.

Mai A, Massa S, Ragno R, Esposito M, Sbardella G, Nocca G, Scatena R, Jesacher F, Loidl P, Brosch G. Mai A, et al. J Med Chem. 2002 Apr 25;45(9):1778-84. doi: 10.1021/jm011088+. J Med Chem. 2002. PMID: 11960489

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