Barbara Cacciari

3.7k citations

108 papers · 3.3k · 1 hit paper · h-index 31

Impact in

Physiology top 0.1%
- Adenosine and Purinergic Signaling
Organic Chemistry top 1%
- Synthesis and Biological Evaluation
- Click Chemistry and Applications
- Synthesis and biological activity

Papers in

Organic Chemistry 75
- Synthesis and Biological Evaluation 37
- Synthesis and Characterization of Heterocyclic Compounds 20
- Synthesis and biological activity 18
- Click Chemistry and Applications 11
Physiology 53
- Adenosine and Purinergic Signaling 53

Co-authors: Giampiero Spalluto (91 shared papers)Pier Giovanni Baraldi (51 shared papers)Romeo Romagnoli (36 shared papers)Pier Andrea Borea (18 shared papers)Katia Varani (18 shared papers)Stefano Moro (30 shared papers)Giorgia Pastorin (24 shared papers)Karl‐Norbert Klotz (25 shared papers)
Journals: Journal of Medicinal Chemistry (22 papers)Bioorganic & Medicinal Chemistry Letters (6 papers)Bioorganic & Medicinal Chemistry (4 papers)Journal of Chemical Information and Modeling (3 papers)Synthesis (3 papers)
Partner nations: Italy Germany United States

In The Last Decade

Barbara Cacciari

108 papers receiving 3.2k citations

Barbara Cacciari's Hit Papers

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Carbon Nanotube Substrates Boost Neuronal Electrical Signaling 2005 · 542 citations

Peers

Countries citing papers authored by Barbara Cacciari

Since Specialization

Citations

This map shows the geographic impact of Barbara Cacciari's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Barbara Cacciari with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Barbara Cacciari more than expected).

Fields of papers citing papers by Barbara Cacciari

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Barbara Cacciari. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Barbara Cacciari. The network helps show where Barbara Cacciari may publish in the future.

Co-authors

The 25 scholars most cited alongside Barbara Cacciari, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Barbara Cacciari Line = papers co-authored together Barbara Cacciari links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 108 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Carbon Nanotube Substrates Boost Neuronal Electrical Signaling Nano Letters ·Viviana Lovat, Davide Pantarotto, Laura Lagostena, Barbara Cacciari, Micaela Grandolfo, Massimo Righi, Giampiero Spalluto, (unknown), Laura Ballerini Hit paper breakdown →	2005	542
2	A_2A-Adenosine Receptor Reserve for Coronary Vasodilation Circulation ·John C. Shryock, Stephen Snowdy, Pier Giovanni Baraldi, Barbara Cacciari, Giampiero Spalluto, Angela Monopoli, Ennio Ongini, Stephen P. Baker, Luiz Belardinelli	1998	164
3	A3 Adenosine Receptor Ligands: History and Perspectives Medicinal Research Reviews ·Pier Giovanni Baraldi, Barbara Cacciari, Romeo Romagnoli, Stefania Merighi, Katia Varani, Pier Andrea Borea, Giampiero Spalluto	2000	124
4	Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine Derivatives: Potent and Selective A_2AAdenosine Antagonists Journal of Medicinal Chemistry ·Pier Giovanni Baraldi, Barbara Cacciari, Giampiero Spalluto, María José Pineda de las Infantas y Villatoro, Cristina Zocchi, Silvio Dionisotti, Ennio Ongini	1996	106
5	[3H]MRE 3008F20: A Novel Antagonist Radioligand for the Pharmacological and Biochemical Characterization of Human A3 Adenosine Receptors Molecular Pharmacology ·Katia Varani, Stefania Merighi, Stefania Gessi, Karl‐Norbert Klotz, Edward Leung, Pier Giovanni Baraldi, Barbara Cacciari, Romeo Romagnoli, Giampiero Spalluto, Pier Andrea Borea	2000	105
6	Synthesis, Biological Activity, and Molecular Modeling Investigation of New Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine Derivatives as Human A₃ Adenosine Receptor Antagonists Journal of Medicinal Chemistry ·Pier Giovanni Baraldi, Barbara Cacciari, Stefano Moro, Giampiero Spalluto, Giorgia Pastorin, Tatiana Da Ros, Karl‐Norbert Klotz, Katia Varani, Stefania Gessi, Pier Andrea Borea	2002	90
7	7-Substituted 5-Amino-2-(2-furyl)pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidines as A_2AAdenosine Receptor Antagonists: A Study on the Importance of Modifications at the Side Chain on the Activity and Solubility Journal of Medicinal Chemistry ·Pier Giovanni Baraldi, Barbara Cacciari, Romeo Romagnoli, Giampiero Spalluto, Angela Monopoli, Ennio Ongini, Katia Varani, Pier Andrea Borea	2001	86
8	Design, Radiosynthesis, and Biodistribution of a New Potent and Selective Ligand for in Vivo Imaging of the Adenosine A_2A Receptor System Using Positron Emission Tomography Journal of Medicinal Chemistry ·Sergio Todde, Rosa Maria Moresco, Pasquale Simonelli, Pier Giovanni Baraldi, Barbara Cacciari, Giampiero Spalluto, Katia Varani, Angela Monopoli, Mario Matarrese, (unknown), Fulvio Magni, M. Galli Kienle, Ferruccio Fazio	2000	84
9	Effect of A-Ring Modifications on the DNA-Binding Behavior and Cytotoxicity of Pyrrolo[2,1-c][1,4]benzodiazepines Journal of Medicinal Chemistry ·David E. Thurston, D. Subhas Bose, Philip W. Howard, Terence C. Jenkins, Alberto Leoni, Pier Giovanni Baraldi, Andrea Guiotto, Barbara Cacciari, Lloyd R. Kèlland, Marie‐Paule Foloppe, Sylvain Rault	1999	75
10	Pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidine Derivatives as Highly Potent and Selective Human A₃Adenosine Receptor Antagonists: Influence of the Chain at the N⁸Pyrazole Nitrogen Journal of Medicinal Chemistry ·Pier Giovanni Baraldi, Barbara Cacciari, Romeo Romagnoli, Giampiero Spalluto, Stefano Moro, Karl‐Norbert Klotz, Edward Leung, Katia Varani, Stefania Gessi, Stefania Merighi, Pier Andrea Borea	2000	73
11	Synthesis, Biological Properties, and Molecular Modeling Investigation of the First Potent, Selective, and Water-Soluble Human A₃ Adenosine Receptor Antagonist Journal of Medicinal Chemistry ·Anna Maconi, Giorgia Pastorin, Tatiana Da Ros, Giampiero Spalluto, Zhan‐Guo Gao, Kenneth A. Jacobson, Pier Giovanni Baraldi, Barbara Cacciari, Katia Varani, Stefano Moro, Pier Andrea Borea	2002	66
12	Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine Derivatives as Highly Potent and Selective Human A₃ Adenosine Receptor Antagonists Journal of Medicinal Chemistry ·Pier Giovanni Baraldi, Barbara Cacciari, Romeo Romagnoli, Giampiero Spalluto, Karl‐Norbert Klotz, Edward Leung, Katia Varani, Stefania Gessi, Stefania Merighi, Pier Andrea Borea	1999	65
13	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 A_2A Adenosine Receptor Antagonists Journal of Medicinal Chemistry ·Pier Giovanni Baraldi, Barbara Cacciari, Giampiero Spalluto, Manuela Bergonzoni, Silvio Dionisotti, Ennio Ongini, Katia Varani, Pier Andrea Borea	1998	62
14	Carbon Nanotubes Carrying Cell‐Adhesion Peptides do not Interfere with Neuronal Functionality Advanced Materials ·Claire Gaillard, Giada Cellot, Shouping Li, Francesca M. Toma, Hélène Dumortier, Giampiero Spalluto, Barbara Cacciari, (unknown), Laura Ballerini, Alberto Bianco	2009	62
15	Synthesis, in Vitro Antiproliferative Activity, and DNA-Binding Properties of Hybrid Molecules Containing Pyrrolo[2,1-c][1,4]benzodiazepine and Minor-Groove-Binding Oligopyrrole Carriers Journal of Medicinal Chemistry ·Pier Giovanni Baraldi, Gianfranco Balboni, Barbara Cacciari, Andrea Guiotto, Stefano Manfredini, Romeo Romagnoli, Giampiero Spalluto, David E. Thurston, Philip W. Howard, Nicoletta Bianchi, Cristina Rutigliano, Carlo Mischiati, Roberto Gambari	1999	59
16	Synthesis and Biological Activity of a New Series of N⁶-Arylcarbamoyl, 2-(Ar)alkynyl-N⁶-arylcarbamoyl, and N⁶-Carboxamido Derivatives of Adenosine-5‘-N-ethyluronamide as A₁ and A₃ Adenosine Receptor Agonists Journal of Medicinal Chemistry ·Pier Giovanni Baraldi, Barbara Cacciari, María José Pineda de las Infantas y Villatoro, Romeo Romagnoli, Giampiero Spalluto, Rosaria Volpini, Stefano Costanzi, Sauro Vittori, Gloria Cristalli, Neli Melman, Kyung Park, Xiao‐duo Ji, Kenneth A. Jacobson	1998	56
17	Combined Target-Based and Ligand-Based Drug Design Approach as a Tool To Define a Novel 3D-Pharmacophore Model of Human A₃Adenosine Receptor Antagonists: Pyrazolo[4,3-e]1,2,4-triazolo[1,5-c]pyrimidine Derivatives as a Key Study Journal of Medicinal Chemistry ·Stefano Moro, Paolo Braiuca, Francesca Deflorian, Cristina Ferrari, Giorgia Pastorin, Barbara Cacciari, Pier Giovanni Baraldi, Katia Varani, Pier Andrea Borea, Giampiero Spalluto	2004	53
18	Pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine Derivatives as Adenosine Receptor Antagonists. Influence of the N5 Substituent on the Affinity at the Human A₃ and A_2B Adenosine Receptor Subtypes: A Molecular Modeling Investigation Journal of Medicinal Chemistry ·Giorgia Pastorin, Tatiana Da Ros, Giampiero Spalluto, Francesca Deflorian, Stefano Moro, Barbara Cacciari, Pier Giovanni Baraldi, Stefania Gessi, Katia Varani, Pier Andrea Borea	2003	52
19	Synthesis and Properties of Substituted CBI Analogs of CC-1065 and the Duocarmycins Incorporating the 7-Methoxy-1,2,9,9a-tetrahydrocyclopropa[c]benz[e]indol-4-one (MCBI) Alkylation Subunit: Magnitude of Electronic Effects on the Functional Reactivity The Journal of Organic Chemistry ·Dale L. Boger, Jeffrey A. McKie, Hui Cai, Barbara Cacciari, P. G. BARALDI	1996	51
20	Oligonucleotides and Oligonucleotide Conjugates: A New Approach for Cancer Treatment Current Medicinal Chemistry ·Tatiana Da Ros, Giampiero Spalluto, (unknown), Tula Saison‐Behmoaras, Alexandre S. Boutorine, Barbara Cacciari	2005	49

About Barbara Cacciari

Barbara Cacciari is a scholar working on Organic Chemistry, Physiology, Molecular Biology, Oncology and Cellular and Molecular Neuroscience, having authored 108 papers that have together received 3.3k indexed citations. Recurring topics across this work include Adenosine and Purinergic Signaling (53 papers), Synthesis and Biological Evaluation (37 papers), Receptor Mechanisms and Signaling (26 papers), Synthesis and Characterization of Heterocyclic Compounds (20 papers), Pharmacological Receptor Mechanisms and Effects (19 papers), Synthesis and biological activity (18 papers), Click Chemistry and Applications (11 papers) and Cancer therapeutics and mechanisms (10 papers). The work is most often cited by research in Physiology (1.3k citations), Organic Chemistry (1.3k citations), Cellular and Molecular Neuroscience (604 citations), Molecular Biology (1.6k citations) and Developmental Neuroscience (50 citations). Barbara Cacciari has collaborated with scholars based in Italy, Germany and United States. Frequent co-authors include Giampiero Spalluto, Pier Giovanni Baraldi, Romeo Romagnoli, Pier Andrea Borea, Katia Varani, Stefano Moro, Giorgia Pastorin, Karl‐Norbert Klotz, Ennio Ongini and Laura Ballerini. Their work appears in journals such as Journal of Medicinal Chemistry, Bioorganic & Medicinal Chemistry Letters, Bioorganic & Medicinal Chemistry, Journal of Chemical Information and Modeling and Synthesis.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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