Pier Giovanni Baraldi

University of Ferrara — Italy

Biochemistry, Genetics and Molecular Biology · Life Sciences

62h-index13.0kcitations426works0.02yr avg
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Research Topics

Adenosine and Purinergic Signaling(127), Synthesis and Biological Evaluation(123), Synthesis and biological activity(82), Synthesis and Characterization of Heterocyclic Compounds(63), Pharmacological Receptor Mechanisms and Effects(58)

Publications426 total

Meet the Editorial Board Member
Cardiovascular & Hematological Agents in Medicinal Chemistry·2022
Meet the Editorial Board Member
Cardiovascular & Hematological Agents in Medicinal Chemistry·2021
Design, Synthesis, and Biological Evaluation of 6-Substituted Thieno[3,2-<i>d</i>]pyrimidine Analogues as Dual Epidermal Growth Factor Receptor Kinase and Microtubule Inhibitors
Journal of Medicinal Chemistry·2019· 46 citedOpen Access
3-Aryl/Heteroaryl-5-amino-1-(3′,4′,5′-trimethoxybenzoyl)-1,2,4-triazoles as antimicrotubule agents. Design, synthesis, antiproliferative activity and inhibition of tubulin polymerization
Bioorganic Chemistry·2018· 21 citedOpen Access
Cover Image, Volume 38, Issue 4
Medicinal Research Reviews·2018Open Access
Discovery of 1,5-Diphenylpyrazole-3-Carboxamide Derivatives as Potent, Reversible, and Selective Monoacylglycerol Lipase (MAGL) Inhibitors
Journal of Medicinal Chemistry·2018· 54 citedOpen Access
Medicinal Chemistry of the A3 Adenosine Receptor
2018· 7 cited
Synthesis and biological evaluation of alpha-bromoacryloylamido indolyl pyridinyl propenones as potent apoptotic inducers in human leukaemia cells
Journal of Enzyme Inhibition and Medicinal Chemistry·2018· 13 citedOpen Access
A2A Adenosine Receptor: Structures, Modeling, and Medicinal Chemistry
2018· 7 citedOpen Access
2-Alkoxycarbonyl-3-arylamino-5-substituted thiophenes as a novel class of antimicrotubule agents: Design, synthesis, cell growth and tubulin polymerization inhibition
European Journal of Medicinal Chemistry·2017· 20 citedOpen Access
A<sub>3</sub>Adenosine Receptors as Modulators of Inflammation: From Medicinal Chemistry to Therapy
Medicinal Research Reviews·2017· 144 citedOpen Access
Design, synthesis and biological evaluation of 3-substituted-2-oxindole hybrid derivatives as novel anticancer agents
European Journal of Medicinal Chemistry·2017· 33 citedOpen Access
Synthesis and Biological Evaluation of 2-Methyl-4,5-Disubstituted Oxazoles as a Novel Class of Highly Potent Antitubulin Agents
Scientific Reports·2017· 25 citedOpen Access
Chemistry of Cannabinoid Receptor Agonists
Elsevier eBooks·2017· 2 cited
Medicinal Chemistry, Pharmacology, and Clinical Implications of TRPV1 Receptor Antagonists
Medicinal Research Reviews·2016· 193 citedOpen Access
Positive allosteric modulation of A1 adenosine receptors as a novel and promising therapeutic strategy for anxiety
Neuropharmacology·2016· 32 citedOpen Access
Design and Synthesis of Potent in Vitro and in Vivo Anticancer Agents Based on 1-(3′,4′,5′-Trimethoxyphenyl)-2-Aryl-1H-Imidazole
Scientific Reports·2016· 35 citedOpen Access
Synthesis and structure activity relationship investigation of triazolo[1,5-a]pyrimidines as CB2 cannabinoid receptor inverse agonists
European Journal of Medicinal Chemistry·2016· 42 citedOpen Access
Medicinal Chemistry, Pharmacology, and Potential Therapeutic Benefits of Cannabinoid CB<sub>2</sub>Receptor Agonists
Chemical Reviews·2016· 111 citedOpen Access
Novel iodoacetamido benzoheterocyclic derivatives with potent antileukemic activity are inhibitors of STAT5 phosphorylation
European Journal of Medicinal Chemistry·2015· 7 citedOpen Access
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Frequent Co-authors

Romeo Romagnoli(22), Pier Andrea Borea(21), Katia Varani(19), Stefania Gessi(18), Mojgan Aghazadeh Tabrizi(17), Stefania Merighi(16), Delia Preti(11), Giampiero Spalluto(10), Barbara Cacciari(9), Edward Leung(7), Andrea Brancale(7), Ernest Hamel(7), Prisco Mirandola(6), Francesca Fruttarolo(5), Maria Giovanna Pavani(5), Daniele Simoni(5), Ennio Ongini(5), M Cara(5), Jan Balzarini(5), Olga Cruz‐López(4)