Barbara Cacciari

3.7k total citations
108 papers, 3.1k citations indexed

About

Barbara Cacciari is a scholar working on Organic Chemistry, Physiology and Molecular Biology. According to data from OpenAlex, Barbara Cacciari has authored 108 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 76 papers in Organic Chemistry, 54 papers in Physiology and 52 papers in Molecular Biology. Recurrent topics in Barbara Cacciari's work include Adenosine and Purinergic Signaling (54 papers), Synthesis and Biological Evaluation (37 papers) and Receptor Mechanisms and Signaling (27 papers). Barbara Cacciari is often cited by papers focused on Adenosine and Purinergic Signaling (54 papers), Synthesis and Biological Evaluation (37 papers) and Receptor Mechanisms and Signaling (27 papers). Barbara Cacciari collaborates with scholars based in Italy, Germany and United States. Barbara Cacciari's co-authors include Giampiero Spalluto, Pier Giovanni Baraldi, Romeo Romagnoli, Pier Andrea Borea, Katia Varani, Stefano Moro, Giorgia Pastorin, Maurizio Prato, Karl‐Norbert Klotz and Ennio Ongini and has published in prestigious journals such as Advanced Materials, Circulation and Nano Letters.

In The Last Decade

Barbara Cacciari

108 papers receiving 3.0k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Barbara Cacciari Italy 31 1.6k 1.3k 1.3k 588 355 108 3.1k
Barrie Kellam United Kingdom 29 1.7k 1.1× 567 0.4× 407 0.3× 594 1.0× 203 0.6× 88 2.5k
Mojgan Aghazadeh Tabrizi Italy 37 1.8k 1.1× 1.9k 1.5× 1.4k 1.1× 469 0.8× 59 0.2× 104 4.0k
Alexandre Specht France 26 942 0.6× 523 0.4× 173 0.1× 695 1.2× 552 1.6× 65 2.5k
Raman Parkesh India 26 990 0.6× 165 0.1× 441 0.3× 223 0.4× 124 0.3× 49 2.5k
Alan Naylor United Kingdom 24 597 0.4× 683 0.5× 130 0.1× 512 0.9× 122 0.3× 72 2.1k
Russell Dahl United States 34 1.7k 1.1× 481 0.4× 85 0.1× 442 0.8× 126 0.4× 71 2.8k
Joseph M. Ready United States 36 902 0.6× 2.7k 2.1× 95 0.1× 226 0.4× 59 0.2× 101 4.1k
Klaus Mohr Germany 37 3.0k 1.9× 340 0.3× 89 0.1× 1.9k 3.1× 115 0.3× 147 3.8k
Gene M. Dubowchik United States 26 1.3k 0.8× 709 0.5× 62 0.0× 173 0.3× 163 0.5× 80 3.0k
Tiziano Bandiera Italy 30 1.1k 0.7× 367 0.3× 42 0.0× 278 0.5× 308 0.9× 89 2.5k

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-authorship network of co-authors of Barbara Cacciari

This figure shows the co-authorship network connecting the top 25 collaborators of Barbara Cacciari. A scholar is included among the top collaborators of Barbara Cacciari based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Barbara Cacciari. Barbara Cacciari is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Oliva, Paola, Romeo Romagnoli, Barbara Cacciari, et al.. (2022). Synthesis and Biological Evaluation of Highly Active 7-Anilino Triazolopyrimidines as Potent Antimicrotubule Agents. Pharmaceutics. 14(6). 1191–1191. 12 indexed citations
2.
Hanau, Stefania, et al.. (2020). Schematic overview of oligosaccharides, with survey on their major physiological effects and a focus on milk ones. Carbohydrate Polymer Technologies and Applications. 1. 100013–100013. 17 indexed citations
3.
Romagnoli, Romeo, Filippo Prencipe, Paola Oliva, et al.. (2020). Synthesis and Biological Evaluation of New Antitubulin Agents Containing 2-(3′,4′,5′-trimethoxyanilino)-3,6-disubstituted-4,5,6,7-tetrahydrothieno[2,3-c]pyridine Scaffold. Molecules. 25(7). 1690–1690. 13 indexed citations
4.
Redenti, Stephen, Antonella Ciancetta, Giorgia Pastorin, et al.. (2016). Pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidines and Structurally Simplified Analogs. Chemistry and SAR Profile as Adenosine Receptor Antagonists. Current Topics in Medicinal Chemistry. 16(28). 3224–3257. 9 indexed citations
5.
Federico, Stephanie, Antonella Ciancetta, Stephen Redenti, et al.. (2015). 5,7-Disubstituted-[1,2,4]triazolo[1,5- a ][1,3,5]triazines as pharmacological tools to explore the antagonist selectivity profiles toward adenosine receptors. European Journal of Medicinal Chemistry. 108. 529–541. 18 indexed citations
6.
Ben, Diego Dal, Michela Buccioni, Catia Lambertucci, et al.. (2013). 8-(2-Furyl)adenine derivatives as A2A adenosine receptor ligands. European Journal of Medicinal Chemistry. 70. 525–535. 13 indexed citations
7.
Cusan, Claudia, Giorgia Pastorin, Giampiero Spalluto, et al.. (2007). Pyrazolo-triazolo-pyrimidines as adenosine receptor antagonists: Effect of the N-5 bond type on the affinity and selectivity at the four adenosine receptor subtypes. Purinergic Signalling. 4(1). 39–46. 10 indexed citations
8.
Cristalli, Gloria, Barbara Cacciari, Diego Dal Ben, et al.. (2006). Highlights on the Development of A2A Adenosine Receptor Agonists and Antagonists. ChemMedChem. 2(3). 260–281. 29 indexed citations
9.
Moro, Stefano, Magdalena Bacilieri, Barbara Cacciari, et al.. (2006). The application of a 3D-QSAR (autoMEP/PLS) approach as an efficient pharmacodynamic-driven filtering method for small-sized virtual library: Application to a lead optimization of a human A3 adenosine receptor antagonist. Bioorganic & Medicinal Chemistry. 14(14). 4923–4932. 24 indexed citations
10.
Cacciari, Barbara, Giampiero Spalluto, Karl‐Norbert Klotz, et al.. (2006). Pyrazolo-triazolo-pyrimidines as adenosine receptor antagonists: A complete structure–activity profile. Purinergic Signalling. 3(3). 183–193. 14 indexed citations
11.
Ros, Tatiana Da, Giampiero Spalluto, Maurizio Prato, et al.. (2005). Oligonucleotides and Oligonucleotide Conjugates: A New Approach for Cancer Treatment. Current Medicinal Chemistry. 12(1). 71–88. 47 indexed citations
12.
13.
Cacciari, Barbara & Giampiero Spalluto. (2005). Non Peptidic αvβ3 Antagonists: Recent Developments. Current Medicinal Chemistry. 12(1). 51–70. 44 indexed citations
14.
Cacciari, Barbara, Giorgia Pastorin, & Giampiero Spalluto. (2003). Medicinal Chemistry of A2A Adenosine Receptor Antagonists. Current Topics in Medicinal Chemistry. 3(4). 403–411. 35 indexed citations
15.
Moro, Stefano, Francesca Deflorian, Giampiero Spalluto, et al.. (2003). Demystifying the three dimensional structure of G protein-coupled receptors (GPCRs) with the aid of molecular modeling. Chemical Communications. 2949–2949. 38 indexed citations
16.
Baraldi, Pier Giovanni, Barbara Cacciari, Giorgia Pastorin, et al.. (2002). Pyrazolo-Triazolo-Pyrimidine Derivatives as Adenosine Receptor Antagonists: A Possible Template for Adenosine Receptor Subtypes?. Current Pharmaceutical Design. 8(26). 2299–2332. 22 indexed citations
17.
Ongini, Ennio, Angela Monopoli, Barbara Cacciari, & Pier Giovanni Baraldi. (2001). Selective adenosine A2A receptor antagonists. Il Farmaco. 56(1-2). 87–90. 39 indexed citations
18.
Todde, Sergio, Pasquale Simonelli, P. G. BARALDI, et al.. (2000). 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. 43(23). 4359–4362. 4 indexed citations
19.
Baraldi, Pier Giovanni, Barbara Cacciari, Romeo Romagnoli, et al.. (2000). Synthesis and preliminary biological evaluation of [3H]-MRE 3008-F20: the first high affinity radioligand antagonist for the human A3 adenosine receptors. Bioorganic & Medicinal Chemistry Letters. 10(3). 209–211. 21 indexed citations
20.
Baraldi, Pier Giovanni, Giampiero Spalluto, Barbara Cacciari, Romeo Romagnoli, & Kenneth D.R. Setchell. (1999). Chemical Synthesis of [ 13 C]Daidzein. Journal of Medicinal Food. 2(3-4). 99–102. 9 indexed citations

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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