P G Baraldi - JoVE Visualize

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Circulation|August 26, 1998

A2A-adenosine receptor reserve for coronary vasodilationJ C Shryock, S Snowdy, P G Baraldi, et al.

Anti-Cancer Drug Design|June 11, 1999

PNU 157977: a new potent antitumour agent exhibiting low in vivo toxicity in mice injected with L1210 leukaemia cellsP G Baraldi, G Balboni, R Romagnoli, et al.

Journal of Medicinal Chemistry|August 10, 2001

Fluorosulfonyl- and bis-(beta-chloroethyl)amino-phenylamino functionalized pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidine derivatives: irreversible antagonists at the human A3 adenosine receptor and molecular modeling studiesP G Baraldi, B Cacciari, S Moro, et al.

Arzneimittel-Forschung|September 1, 1988

Synthesis of 1H-pyrazolo[4,3-d]pyrimidine-7(6H)-ones and pyrazolo-5-carboxamides and interaction with benzodiazepine and adenosine A1 receptors in rat cerebral cortexP G Baraldi, A Casolari, S Manfredini, et al.

Journal of Medicinal Chemistry|March 1, 1996

Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine derivatives: potent and selective A(2A) adenosine antagonistsP G Baraldi, B Cacciari, G Spalluto, et al.

Drug Design and Discovery|February 1, 1992

New isoxazole derivatives of retinoids: synthesis and activity on growth and differentiation of tumor cellsD Simoni, S Manfredini, M A Tabrizi, et al.

Nucleosides, Nucleotides & Nucleic Acids|August 26, 2000

Pyrazole related nucleosides 5. Synthesis and biological activity of 2'-deoxy-2',3'-dideoxy- and acyclo-analogues of 4-iodo-1-beta-D-ribofuranosyl-3-carboxymethyl pyrazole (IPCAR)S Manfredini, P G Baraldi, R Bazzanini, et al.

Bioorganic & Medicinal Chemistry Letters|June 8, 2001

Design, synthesis and enzymatic activity of highly selective human mitochondrial thymidine kinase inhibitorsS Manfredini, P G Baraldi, E Durini, et al.

Journal of Medicinal Chemistry|September 1, 1978

Synthesis and prostaglandin-like activity of 2-(trans-3-hydroxy-1-octenyl)-3-indoleheptanoic acidA Barco, S Benetti, G P Pollini, et al.

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

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 reactivityP G Baraldi, B Cacciari, A Guiotto, et al.

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Showing results (51-60 of 74) with videos related to

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Circulation|August 26, 1998

A2A-adenosine receptor reserve for coronary vasodilationJ C Shryock, S Snowdy, P G Baraldi, et al.

Anti-Cancer Drug Design|June 11, 1999

PNU 157977: a new potent antitumour agent exhibiting low in vivo toxicity in mice injected with L1210 leukaemia cellsP G Baraldi, G Balboni, R Romagnoli, et al.

Journal of Medicinal Chemistry|August 10, 2001

Fluorosulfonyl- and bis-(beta-chloroethyl)amino-phenylamino functionalized pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidine derivatives: irreversible antagonists at the human A3 adenosine receptor and molecular modeling studiesP G Baraldi, B Cacciari, S Moro, et al.

Arzneimittel-Forschung|September 1, 1988

Synthesis of 1H-pyrazolo[4,3-d]pyrimidine-7(6H)-ones and pyrazolo-5-carboxamides and interaction with benzodiazepine and adenosine A1 receptors in rat cerebral cortexP G Baraldi, A Casolari, S Manfredini, et al.

Journal of Medicinal Chemistry|March 1, 1996

Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine derivatives: potent and selective A(2A) adenosine antagonistsP G Baraldi, B Cacciari, G Spalluto, et al.

Drug Design and Discovery|February 1, 1992

New isoxazole derivatives of retinoids: synthesis and activity on growth and differentiation of tumor cellsD Simoni, S Manfredini, M A Tabrizi, et al.

Nucleosides, Nucleotides & Nucleic Acids|August 26, 2000

Pyrazole related nucleosides 5. Synthesis and biological activity of 2'-deoxy-2',3'-dideoxy- and acyclo-analogues of 4-iodo-1-beta-D-ribofuranosyl-3-carboxymethyl pyrazole (IPCAR)S Manfredini, P G Baraldi, R Bazzanini, et al.

Bioorganic & Medicinal Chemistry Letters|June 8, 2001

Design, synthesis and enzymatic activity of highly selective human mitochondrial thymidine kinase inhibitorsS Manfredini, P G Baraldi, E Durini, et al.

Journal of Medicinal Chemistry|September 1, 1978

Synthesis and prostaglandin-like activity of 2-(trans-3-hydroxy-1-octenyl)-3-indoleheptanoic acidA Barco, S Benetti, G P Pollini, et al.

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

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 reactivityP G Baraldi, B Cacciari, A Guiotto, et al.

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