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B Cacciari

Showing results (11-20 of 36) with videos related to

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International Journal of Cosmetic Science|February 28, 2009
Cosmetic preservation and structure-activity relationships of 4-diazo-pyrazole-5-carboxamidesP G Baraldi, M Guarneri, S Bader, et al.
Journal of Medicinal Chemistry|December 9, 1994
Synthesis and antitumor activity of a new class of pyrazolo[4,3-e]pyrrolo[1,2-a][1,4]diazepinone analogues of pyrrolo[1,4][2,1-c]benzodiazepinesP G Baraldi, A Leoni, B Cacciari, et al.
Farmaco (Societa Chimica Italiana : 1989)|June 18, 2005
Synthesis, biological and modeling studies of 1,3-di-n-propyl-2,4-dioxo-6-methyl-8-(substituted) 1,2,3,4-tetrahydro [1,2,4]-triazolo [3,4-f]-purines as adenosine receptor antagonistsG Pastorin, C Bolcato, B Cacciari, 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.
Anti-Cancer Drug Design|January 1, 1997
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-1065P G Baraldi, B Cacciari, M J Pineda de las Infantas, 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.
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.
Farmaco (Societa Chimica Italiana : 1989)|April 1, 1996
1,2,3-Triazolo[5,4-e]1,2,4-triazolo[1,5-c]pyrimidine derivatives: a new class of A2A adenosine receptor antagonistsP G Baraldi, B Cacciari, G Spalluto, et al.
Circulation|August 26, 1998
A2A-adenosine receptor reserve for coronary vasodilationJ C Shryock, S Snowdy, P G Baraldi, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

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Pageof 4
International Journal of Cosmetic Science|February 28, 2009
Cosmetic preservation and structure-activity relationships of 4-diazo-pyrazole-5-carboxamidesP G Baraldi, M Guarneri, S Bader, et al.
Journal of Medicinal Chemistry|December 9, 1994
Synthesis and antitumor activity of a new class of pyrazolo[4,3-e]pyrrolo[1,2-a][1,4]diazepinone analogues of pyrrolo[1,4][2,1-c]benzodiazepinesP G Baraldi, A Leoni, B Cacciari, et al.
Farmaco (Societa Chimica Italiana : 1989)|June 18, 2005
Synthesis, biological and modeling studies of 1,3-di-n-propyl-2,4-dioxo-6-methyl-8-(substituted) 1,2,3,4-tetrahydro [1,2,4]-triazolo [3,4-f]-purines as adenosine receptor antagonistsG Pastorin, C Bolcato, B Cacciari, 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.
Anti-Cancer Drug Design|January 1, 1997
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-1065P G Baraldi, B Cacciari, M J Pineda de las Infantas, 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.
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.
Farmaco (Societa Chimica Italiana : 1989)|April 1, 1996
1,2,3-Triazolo[5,4-e]1,2,4-triazolo[1,5-c]pyrimidine derivatives: a new class of A2A adenosine receptor antagonistsP G Baraldi, B Cacciari, G Spalluto, et al.
Circulation|August 26, 1998
A2A-adenosine receptor reserve for coronary vasodilationJ C Shryock, S Snowdy, P G Baraldi, et al.
Pageof 4