Cacciari B - Search Results

1

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: cacciari b. Arzneimittelforschung. 1996 Apr;46(4):365-8. Arzneimittelforschung. 1996. PMID: 8740079

2

7-Substituted 5-amino-2-(2-furyl)pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidines as A2A adenosine receptor antagonists: a study on the importance of modifications at the side chain on the activity and solubility.

Baraldi PG, Cacciari B, Romagnoli R, Spalluto G, Monopoli A, Ongini E, Varani K, Borea PA. Baraldi PG, et al. Among authors: cacciari b. J Med Chem. 2002 Jan 3;45(1):115-26. doi: 10.1021/jm010924c. J Med Chem. 2002. PMID: 11754583

3

Synthesis, biological activity, and molecular modeling investigation of new pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine derivatives as human A(3) adenosine receptor antagonists.

Baraldi PG, Cacciari B, Moro S, Spalluto G, Pastorin G, Da Ros T, Klotz KN, Varani K, Gessi S, Borea PA. Baraldi PG, et al. Among authors: cacciari b. J Med Chem. 2002 Feb 14;45(4):770-80. doi: 10.1021/jm0109614. J Med Chem. 2002. PMID: 11831890

4

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: cacciari b. J Med Chem. 1996 Feb 2;39(3):802-6. doi: 10.1021/jm950518r. J Med Chem. 1996. PMID: 8576924

5

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: cacciari b. Farmaco. 1996 Apr;51(4):297-300. Farmaco. 1996. PMID: 8645419 No abstract available.

6

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: cacciari b. J Med Chem. 1996 Mar 1;39(5):1164-71. doi: 10.1021/jm950746l. J Med Chem. 1996. PMID: 8676354

7

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: cacciari b. J Med Chem. 1998 Jun 4;41(12):2126-33. doi: 10.1021/jm9708689. J Med Chem. 1998. PMID: 9622554

8

Synthesis and biological activity of a new series of N6-arylcarbamoyl, 2-(Ar)alkynyl-N6-arylcarbamoyl, and N6-carboxamido derivatives of adenosine-5'-N-ethyluronamide as A1 and A3 adenosine receptor agonists.

Baraldi PG, Cacciari B, Pineda de Las Infantas MJ, Romagnoli R, Spalluto G, Volpini R, Costanzi S, Vittori S, Cristalli G, Melman N, Park KS, Ji XD, Jacobson KA. Baraldi PG, et al. Among authors: cacciari b. J Med Chem. 1998 Aug 13;41(17):3174-85. doi: 10.1021/jm980147p. J Med Chem. 1998. PMID: 9703463 Free PMC article.

9

Binding affinity of adenosine receptor agonists and antagonists at human cloned A3 adenosine receptors.

Varani K, Cacciari B, Baraldi PG, Dionisotti S, Ongini E, Borea PA. Varani K, et al. Among authors: cacciari b. Life Sci. 1998;63(5):PL 81-7. doi: 10.1016/s0024-3205(98)00289-6. Life Sci. 1998. PMID: 9714428

10

1H-pyrazolo[2,3-d][1,2,4]triazine-3,7-diones as a new class of human leukocyte elastase inhibitors.

Baraldi PG, Cacciari B, Romagnoli R, Spalluto G. Baraldi PG, et al. Among authors: cacciari b. Arzneimittelforschung. 1999 Dec;49(12):997-1000. doi: 10.1055/s-0031-1300540. Arzneimittelforschung. 1999. PMID: 10635444

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