Spalluto G - Search Results

1

Synthesis, biological properties, and molecular modeling investigation of the first potent, selective, and water-soluble human A(3) adenosine receptor antagonist.

Maconi A, Pastorin G, Da Ros T, Spalluto G, Gao ZG, Jacobson KA, Baraldi PG, Cacciari B, Varani K, Moro S, Borea PA. Maconi A, et al. Among authors: spalluto g. J Med Chem. 2002 Aug 15;45(17):3579-82. doi: 10.1021/jm020974x. J Med Chem. 2002. PMID: 12166930 Free PMC article.

2

Novel N6-(substituted-phenylcarbamoyl)adenosine-5'-uronamides as potent agonists for A3 adenosine receptors.

Baraldi PG, Cacciari B, Spalluto G, Ji XD, Olah ME, Stiles G, Dionisotti S, Zocchi C, Ongini E, Jacobson KA. Baraldi PG, et al. Among authors: spalluto g. J Med Chem. 1996 Feb 2;39(3):802-6. doi: 10.1021/jm950518r. J Med Chem. 1996. PMID: 8576924

3

1,2,3-Triazolo[5,4-e]1,2,4-triazolo[1,5-c]pyrimidine derivatives: a new class of A2A adenosine receptor antagonists.

Baraldi PG, Cacciari B, Spalluto G, Pineda de las Infants MJ, Zocchi C, Ferrara S, Dionisotti S, FerraDDionisotti S. Baraldi PG, et al. Among authors: spalluto g. Farmaco. 1996 Apr;51(4):297-300. Farmaco. 1996. PMID: 8645419 No abstract available.

4

Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine derivatives: potent and selective A(2A) adenosine antagonists.

Baraldi PG, Cacciari B, Spalluto G, Pineda de las Infantas y Villatoro MJ, Zocchi C, Dionisotti S, Ongini E. Baraldi PG, et al. Among authors: spalluto g. J Med Chem. 1996 Mar 1;39(5):1164-71. doi: 10.1021/jm950746l. J Med Chem. 1996. PMID: 8676354

5

1H-pyrazolo[4,3-d]pyrimidine-7(6H)-one and 5H-pyrazolo[4,3-d] 1,2,3-triazin-4(3H)-one derivatives. Synthesis and in vitro biological activity at adenosine A1 and A2a receptors.

Baraldi PG, Cacciari B, Dalpiaz A, Dionisotti S, Zocchi C, Pineda de las Infantas MJ, Spalluto G, Varani K. Baraldi PG, et al. Among authors: spalluto g. Arzneimittelforschung. 1996 Apr;46(4):365-8. Arzneimittelforschung. 1996. PMID: 8740079

6

Synthesis, chemical solvolytic stability and preliminary biological evaluation of (+/-)-N-Boc-CPzI: a pyrazole analog of the left-hand segment of the antitumor agent CC-1065.

Baraldi PG, Cacciari B, Pineda de las Infantas MJ, Romagnoli R, Spalluto G, Cozzi P, Mongelli N. Baraldi PG, et al. Among authors: spalluto g. Anticancer Drug Des. 1997 Jan;12(1):67-74. Anticancer Drug Des. 1997. PMID: 9051115 No abstract available.

7

Synthesis, cytotoxicity, antitumor activity and sequence selective binding of two pyrazole analogs structurally related to the antitumor agents U-71,184 and adozelesin.

Baraldi PG, Cacciari B, Romagnoli R, Spalluto G, Gambari R, Bianchi N, Passadore M, Ambrosino P, Mongelli N, Cozzi P, Geroni C. Baraldi PG, et al. Among authors: spalluto g. Anticancer Drug Des. 1997 Oct;12(7):555-76. Anticancer Drug Des. 1997. PMID: 9365502

8

Design, synthesis, and biological evaluation of a second generation of pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidines as potent and selective A2A adenosine receptor antagonists.

Baraldi PG, Cacciari B, Spalluto G, Bergonzoni M, Dionisotti S, Ongini E, Varani K, Borea PA. Baraldi PG, et al. Among authors: spalluto g. J Med Chem. 1998 Jun 4;41(12):2126-33. doi: 10.1021/jm9708689. J Med Chem. 1998. PMID: 9622554

9

Synthesis, cytotoxicity and antitumor activity of some new simplified pyrazole analogs of the antitumor agent CC-1065. Effect of an hydrophobic group on antitumor activity.

Baraldi PG, Cacciari B, Guiotto A, Romagnoli R, Spalluto G, Zaid AN, Cozzi P, Geroni C, Mongelli N. Baraldi PG, et al. Among authors: spalluto g. Farmaco. 1997 Dec;52(12):711-6. Farmaco. 1997. PMID: 9648274

10

Synthesis, solvolytic stability and cytotoxicity of a modified derivative of CPzI, a pyrazole analog of the alkylation subunit of the antitumor agent CC-1065: effect of the nitrogen substitution on the functional reactivity.

Baraldi PG, Cacciari B, Guiotto A, Romagnoli R, Spalluto G, Zaid AN, Capolongo L, Cozzi P, Geroni C, Mongelli N. Baraldi PG, et al. Among authors: spalluto g. Farmaco. 1997 Dec;52(12):717-23. Farmaco. 1997. PMID: 9648275

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