P G Baraldi - JoVE Visualize

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Nucleosides & Nucleotides|August 5, 1999

Synthesis, cytostatic activity and inhibition of ribonucleotide reductase by 5'-phosphoramidates and 5'-diphosphates, of 2'-O-allyl-arabinofuranosyl nucleosidesS Manfredini, P G Baraldi, E Durini, et al.

Journal of Medicinal Chemistry|June 17, 1998

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 antagonistsP G Baraldi, B Cacciari, G Spalluto, et al.

Journal of Medicinal Chemistry|July 14, 2000

Synthesis and antitumor activity of new benzoheterocyclic derivatives of distamycin AP G Baraldi, R Romagnoli, I Beria, et al.

Anticancer Research|September 1, 1989

New synthetic retinoids: effects on proliferation and differentiationC Nastruzzi, D Simoni, S Manfredini, et al.

Farmaco (Societa Chimica Italiana : 1989)|November 1, 1991

Synthesis, antibacterial activity and structure-activity relationships of N-substituted 4-diazo-pyrazole-5-carboxamides. 2P G Baraldi, B Cacciari, A Leoni, et al.

Journal of Medicinal Chemistry|August 28, 1999

5'-Phosphoramidates and 5'-diphosphates of 2'-O-allyl-beta-D-arabinofuranosyluracil, -cytosine, and -adenine: inhibition of ribonucleotide reductaseS Manfredini, P G Baraldi, E Durini, et al.

British Journal of Pharmacology|August 28, 2001

Pharmacological and biochemical characterization of A3 adenosine receptors in Jurkat T cellsS Gessi, K Varani, S Merighi, et al.

Farmaco (Societa Chimica Italiana : 1989)|July 2, 1998

Synthesis, cytotoxicity and antitumor activity of some new simplified pyrazole analogs of the antitumor agent CC-1065. Effect of an hydrophobic group on antitumor activityP G Baraldi, B Cacciari, A Guiotto, et al.

Arzneimittel-Forschung|April 1, 1996

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 receptorsP G Baraldi, B Cacciari, A Dalpiaz, et al.

Journal of Medicinal Chemistry|March 6, 1992

Pyrazole-related nucleosides. Synthesis and antiviral/antitumor activity of some substituted pyrazole and pyrazolo[4,3-d]-1,2,3-triazin-4-one nucleosidesS Manfredini, R Bazzanini, P G Baraldi, et al.

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Nucleosides & Nucleotides|August 5, 1999

Synthesis, cytostatic activity and inhibition of ribonucleotide reductase by 5'-phosphoramidates and 5'-diphosphates, of 2'-O-allyl-arabinofuranosyl nucleosidesS Manfredini, P G Baraldi, E Durini, et al.

Journal of Medicinal Chemistry|June 17, 1998

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 antagonistsP G Baraldi, B Cacciari, G Spalluto, et al.

Journal of Medicinal Chemistry|July 14, 2000

Synthesis and antitumor activity of new benzoheterocyclic derivatives of distamycin AP G Baraldi, R Romagnoli, I Beria, et al.

Anticancer Research|September 1, 1989

New synthetic retinoids: effects on proliferation and differentiationC Nastruzzi, D Simoni, S Manfredini, et al.

Farmaco (Societa Chimica Italiana : 1989)|November 1, 1991

Synthesis, antibacterial activity and structure-activity relationships of N-substituted 4-diazo-pyrazole-5-carboxamides. 2P G Baraldi, B Cacciari, A Leoni, et al.

Journal of Medicinal Chemistry|August 28, 1999

5'-Phosphoramidates and 5'-diphosphates of 2'-O-allyl-beta-D-arabinofuranosyluracil, -cytosine, and -adenine: inhibition of ribonucleotide reductaseS Manfredini, P G Baraldi, E Durini, et al.

British Journal of Pharmacology|August 28, 2001

Pharmacological and biochemical characterization of A3 adenosine receptors in Jurkat T cellsS Gessi, K Varani, S Merighi, et al.

Farmaco (Societa Chimica Italiana : 1989)|July 2, 1998

Synthesis, cytotoxicity and antitumor activity of some new simplified pyrazole analogs of the antitumor agent CC-1065. Effect of an hydrophobic group on antitumor activityP G Baraldi, B Cacciari, A Guiotto, et al.

Arzneimittel-Forschung|April 1, 1996

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 receptorsP G Baraldi, B Cacciari, A Dalpiaz, et al.

Journal of Medicinal Chemistry|March 6, 1992

Pyrazole-related nucleosides. Synthesis and antiviral/antitumor activity of some substituted pyrazole and pyrazolo[4,3-d]-1,2,3-triazin-4-one nucleosidesS Manfredini, R Bazzanini, P G Baraldi, et al.

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