Balboni G - Search Results

1

PNU 157977: a new potent antitumour agent exhibiting low in vivo toxicity in mice injected with L1210 leukaemia cells.

Baraldi PG, Balboni G, Romagnoli R, Spalluto G, Cozzi P, Geroni C, Mongelli N, Rutigliano C, Bianchi N, Gambari R. Baraldi PG, et al. Among authors: balboni g. Anticancer Drug Des. 1999 Feb;14(1):71-6. Anticancer Drug Des. 1999. PMID: 10363029

2

Synthesis, in vitro antiproliferative activity, and DNA-binding properties of hybrid molecules containing pyrrolo[2,1-c][1, 4]benzodiazepine and minor-groove-binding oligopyrrole carriers.

Baraldi PG, Balboni G, Cacciari B, Guiotto A, Manfredini S, Romagnoli R, Spalluto G, Thurston DE, Howard PW, Bianchi N, Rutigliano C, Mischiati C, Gambari R. Baraldi PG, et al. Among authors: balboni g. J Med Chem. 1999 Dec 16;42(25):5131-41. doi: 10.1021/jm991033w. J Med Chem. 1999. PMID: 10602698

3

Design, synthesis, DNA binding, and biological evaluation of water-soluble hybrid molecules containing two pyrazole analogues of the alkylating cyclopropylpyrroloindole (CPI) subunit of the antitumor agent CC-1065 and polypyrrole minor groove binders.

Baraldi PG, Balboni G, Pavani MG, Spalluto G, Tabrizi MA, Clercq ED, Balzarini J, Bando T, Sugiyama H, Romagnoli R. Baraldi PG, et al. Among authors: balboni g. J Med Chem. 2001 Aug 2;44(16):2536-43. doi: 10.1021/jm0108404. J Med Chem. 2001. PMID: 11472207

4

From the potent and selective mu opioid receptor agonist H-Dmt-d-Arg-Phe-Lys-NH(2) to the potent delta antagonist H-Dmt-Tic-Phe-Lys(Z)-OH.

Balboni G, Cocco MT, Salvadori S, Romagnoli R, Sasaki Y, Okada Y, Bryant SD, Jinsmaa Y, Lazarus LH. Balboni G, et al. J Med Chem. 2005 Aug 25;48(17):5608-11. doi: 10.1021/jm0504959. J Med Chem. 2005. PMID: 16107162

5

Design, Synthesis and Evaluation of Antiproliferative Activity of New Benzimidazolehydrazones.

Onnis V, Demurtas M, Deplano A, Balboni G, Baldisserotto A, Manfredini S, Pacifico S, Liekens S, Balzarini J. Onnis V, et al. Among authors: balboni g. Molecules. 2016 Apr 30;21(5):579. doi: 10.3390/molecules21050579. Molecules. 2016. PMID: 27144551 Free PMC article.

6

New features of the delta opioid receptor: conformational properties of deltorphin I analogues.

Balboni G, Marastoni M, Picone D, Salvadori S, Tancredi T, Temussi PA, Tomatis R. Balboni G, et al. Biochem Biophys Res Commun. 1990 Jun 15;169(2):617-22. doi: 10.1016/0006-291x(90)90375-w. Biochem Biophys Res Commun. 1990. PMID: 2162669

7

Design and solution structure of a partially rigid opioid antagonist lacking the basic center--models of antagonism.

Crescenzi O, Fraternali F, Picone D, Tancredi T, Balboni G, Guerrini R, Lazarus LH, Salvadori S, Temussi PA. Crescenzi O, et al. Among authors: balboni g. Eur J Biochem. 1997 Jul 1;247(1):66-73. doi: 10.1111/j.1432-1033.1997.t01-1-00066.x. Eur J Biochem. 1997. PMID: 9249010 Free article.

8

Design of mu selective opioid dipeptide antagonists.

Capasso A, Amodeo P, Balboni G, Guerrini R, Lazarus LH, Temussi PA, Salvadori S. Capasso A, et al. Among authors: balboni g. FEBS Lett. 1997 Nov 3;417(1):141-4. doi: 10.1016/s0014-5793(97)01271-4. FEBS Lett. 1997. PMID: 9395092 Free article.

9

Synthesis and structure-activity relationships of deltorphin analogues.

Salvadori S, Marastoni M, Balboni G, Borea PA, Morari M, Tomatis R. Salvadori S, et al. Among authors: balboni g. J Med Chem. 1991 May;34(5):1656-61. doi: 10.1021/jm00109a019. J Med Chem. 1991. PMID: 1851843

10

Structure-activity relationships of peptide T-related pentapeptides.

Marastoni M, Salvadori S, Balboni G, Spisani S, Gavioli R, Traniello S, Tomatis R. Marastoni M, et al. Among authors: balboni g. Arzneimittelforschung. 1989 Aug;39(8):926-8. Arzneimittelforschung. 1989. PMID: 2818682

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