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Bioorganic & Medicinal Chemistry Letters|March 4, 2000

Synthesis and preliminary biological evaluation of [3H]-MRE 3008-F20: the first high affinity radioligand antagonist for the human A3 adenosine receptorsP G Baraldi, B Cacciari, R Romagnoli, et al.

Molecular Pharmacology|April 25, 2000

[(3)H]MRE 3008F20: a novel antagonist radioligand for the pharmacological and biochemical characterization of human A(3) adenosine receptorsK Varani, S Merighi, S Gessi, et al.

Nucleosides, Nucleotides & Nucleic Acids|November 30, 2000

[2,1-c][1,4]benzodiazepine (PBD)-distamycin hybrid inhibits DNA binding to transcription factor Sp1P G Baraldi, B Cacciari, A Guiotto, et al.

Bioorganic & Medicinal Chemistry Letters|September 15, 2000

Synthesis and biological effects of a new series of 2-amino-3-benzoylthiophenes as allosteric enhancers of A1-adenosine receptorP G Baraldi, A N Zaid, I Lampronti, et al.

Anti-Cancer Drug Design|November 20, 1997

Synthesis, cytotoxicity, antitumor activity and sequence selective binding of two pyrazole analogs structurally related to the antitumor agents U-71,184 and adozelesinP G Baraldi, B Cacciari, R Romagnoli, et al.

Journal of Medicinal Chemistry|February 2, 1996

Novel N6-(substituted-phenylcarbamoyl)adenosine-5'-uronamides as potent agonists for A3 adenosine receptorsP G Baraldi, B Cacciari, G Spalluto, et al.

Journal of Medicinal Chemistry|July 27, 2001

Design, synthesis, DNA binding, and biological evaluation of water-soluble hybrid molecules containing two pyrazole analogues of the alkylating cyclopropylpyrroloindole (CPI) subunit of the antitumor agent CC-1065 and polypyrrole minor groove bindersP G Baraldi, G Balboni, M G Pavani, et al.

Anti-Cancer Drug Design|April 1, 1996

Pyrazole-related nucleosides. 4. Synthesis and antitumor activity of some 1-tetrahydropyranyl-4-substituted pyrazolesS Manfredini, R Bazzanini, P G Baraldi, et al.

Bioorganic & Medicinal Chemistry Letters|January 5, 1999

Design, synthesis and biological activity of a pyrrolo [2,1-c][1,4]benzodiazepine (PBD)-distamycin hybridP G Baraldi, B Cacciari, A Guiotto, et al.

Journal of Medicinal Chemistry|December 22, 2000

Pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidine derivatives as highly potent and selective human A(3) adenosine receptor antagonists: influence of the chain at the N(8) pyrazole nitrogenP G Baraldi, B Cacciari, R Romagnoli, et al.

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Bioorganic & Medicinal Chemistry Letters|March 4, 2000

Synthesis and preliminary biological evaluation of [3H]-MRE 3008-F20: the first high affinity radioligand antagonist for the human A3 adenosine receptorsP G Baraldi, B Cacciari, R Romagnoli, et al.

Molecular Pharmacology|April 25, 2000

[(3)H]MRE 3008F20: a novel antagonist radioligand for the pharmacological and biochemical characterization of human A(3) adenosine receptorsK Varani, S Merighi, S Gessi, et al.

Nucleosides, Nucleotides & Nucleic Acids|November 30, 2000

[2,1-c][1,4]benzodiazepine (PBD)-distamycin hybrid inhibits DNA binding to transcription factor Sp1P G Baraldi, B Cacciari, A Guiotto, et al.

Bioorganic & Medicinal Chemistry Letters|September 15, 2000

Synthesis and biological effects of a new series of 2-amino-3-benzoylthiophenes as allosteric enhancers of A1-adenosine receptorP G Baraldi, A N Zaid, I Lampronti, et al.

Anti-Cancer Drug Design|November 20, 1997

Synthesis, cytotoxicity, antitumor activity and sequence selective binding of two pyrazole analogs structurally related to the antitumor agents U-71,184 and adozelesinP G Baraldi, B Cacciari, R Romagnoli, et al.

Journal of Medicinal Chemistry|February 2, 1996

Novel N6-(substituted-phenylcarbamoyl)adenosine-5'-uronamides as potent agonists for A3 adenosine receptorsP G Baraldi, B Cacciari, G Spalluto, et al.

Journal of Medicinal Chemistry|July 27, 2001

Design, synthesis, DNA binding, and biological evaluation of water-soluble hybrid molecules containing two pyrazole analogues of the alkylating cyclopropylpyrroloindole (CPI) subunit of the antitumor agent CC-1065 and polypyrrole minor groove bindersP G Baraldi, G Balboni, M G Pavani, et al.

Anti-Cancer Drug Design|April 1, 1996

Pyrazole-related nucleosides. 4. Synthesis and antitumor activity of some 1-tetrahydropyranyl-4-substituted pyrazolesS Manfredini, R Bazzanini, P G Baraldi, et al.

Bioorganic & Medicinal Chemistry Letters|January 5, 1999

Design, synthesis and biological activity of a pyrrolo [2,1-c][1,4]benzodiazepine (PBD)-distamycin hybridP G Baraldi, B Cacciari, A Guiotto, et al.

Journal of Medicinal Chemistry|December 22, 2000

Pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidine derivatives as highly potent and selective human A(3) adenosine receptor antagonists: influence of the chain at the N(8) pyrazole nitrogenP G Baraldi, B Cacciari, R Romagnoli, et al.

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