Giuliana Biagi

886 citations

46 papers · 683 indexed · h-index 17

Physiology top 5%
- Adenosine and Purinergic Signaling 17
Organic Chemistry top 5%
- Synthesis and Biological Evaluation 26
- Synthesis and Characterization of Heterocyclic Compounds 17
- Click Chemistry and Applications 12
- Synthesis and biological activity 6
- Quinazolinone synthesis and applications 5
Molecular Biology
- Phenothiazines and Benzothiazines Synthesis and Activities 6
- Ion channel regulation and function 5
Toxicology
Nephrology

Co-authors: Oreste Livi Irene Giorgi Valerio Scartoni Vincenzo Calderone Enrica Martinotti P. L. BARILI Gino Giannaccini Laura Betti
Cited by: Physiology Organic Chemistry Molecular Biology
Journals: Journal of Medicinal Chemistry (2 papers)The Journal of Organic Chemistry (1 paper)European Journal of Medicinal Chemistry (10 papers)
Partner nations: Italy United States

In The Last Decade

Giuliana Biagi

45 papers receiving 655 citations

Peers

Countries citing papers authored by Giuliana Biagi

Since Specialization

Citations

This map shows the geographic impact of Giuliana Biagi'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 Giuliana Biagi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Giuliana Biagi more than expected).

Fields of papers citing papers by Giuliana Biagi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Giuliana Biagi. 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 Giuliana Biagi. The network helps show where Giuliana Biagi may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Giuliana Biagi, 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 Giuliana Biagi Line = papers co-authored together Giuliana Biagi links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Synthesis, biological assays and QSAR studies of N-(9-benzyl-2-phenyl-8-azapurin-6-yl)-amides as ligands for A1 adenosine receptors Bioorganic & Medicinal Chemistry ·Irene Giorgi,Michele Leonardi,Daniele Pietra,Giuliana Biagi,Alice Borghini,Ilaria Massarelli,Osele Ciampi,Anna Maria Bianucci	2009	6
2	N6-1,3-Diphenylurea derivatives of 2-phenyl-9-benzyladenines and 8-azaadenines: Synthesis and biological evaluation as allosteric modulators of A2A adenosine receptors European Journal of Medicinal Chemistry ·Irene Giorgi,Giuliana Biagi,Anna Maria Bianucci,Alice Borghini,Oreste Livi,Michele Leonardi,Daniele Pietra,Vincenzo Calderone,Alma Martelli	2007	21
3	Synthesis of New 2‐Phenyladenines and 2‐Phenylpteridines and Biological Evaluation as Adenosine Receptor Ligands Archiv der Pharmazie ·Irene Giorgi,Giuliana Biagi,Oreste Livi,Michele Leonardi,Valerio Scartoni,Daniele Pietra	2007	3
4	Synthesis, biological activity and molecular modelling of new trisubstituted 8-azaadenines with high affinity for A1 adenosine receptors European Journal of Medicinal Chemistry ·Irene Giorgi,Anna Maria Bianucci,Giuliana Biagi,Oreste Livi,Valerio Scartoni,Michele Leonardi,Daniele Pietra,Alessio Coi,Ilaria Massarelli,Fatena Ahmad Nofal,Francesca Lidia Fiamingo,P. Anastasi,Stefano Giannini	2006	25
5	2,9-Disubstituted-N6-(arylcarbamoyl)-8-azaadenines as new selective A3 adenosine receptor antagonists: Synthesis, biochemical and molecular modelling studies Bioorganic & Medicinal Chemistry ·Giuliana Biagi,Anna Maria Bianucci,Alessio Coi,Barbara Costa,Laura Fabbrini,Irene Giorgi,Oreste Livi,Iolanda Micco,Federica Pacchini,E. Santini,Michele Leonardi,Fatena Ahmad Nofal,Oreste LeRoy Salerni,Valerio Scartoni	2005	17
6	Synthesis and biological activity of novel substituted benzanilides as potassium channel activators. V European Journal of Medicinal Chemistry ·Giuliana Biagi,Irene Giorgi,Oreste Livi,Antônio Egídio Nardi,Vincenzo Calderone,Alma Martelli,Enrica Martinotti,Oreste LeRoy Salerni	2004	40
7	1,5-Diarylsubstituted 1,2,3-triazoles as potassium channel activators. VI Il Farmaco ·Giuliana Biagi,Vincenzo Calderone,Irene Giorgi,Oreste Livi,Enrica Martinotti,Alma Martelli,Antônio Egídio Nardi	2004	37
8	New N6- or N(9)-hydroxyalkyl substituted 8-azaadenines or adenines as effective A1 adenosine receptor ligands European Journal of Medicinal Chemistry ·Giuliana Biagi,Irene Giorgi,Michele Leonardi,Oreste Livi,Federica Pacchini,Valerio Scartoni,Barbara Costa,Antonio Lucacchini	2003	7
9	N6-Cycloalkyl-2-phenyl-3-deaza-8-azaadenines: a new class of A1 adenosine receptor ligands. A comparison with the corresponding adenines and 8-azaadenines European Journal of Medicinal Chemistry ·Giuliana Biagi,Irene Giorgi,Oreste Livi,Antônio Egídio Nardi,Federica Pacchini,Valerio Scartoni,Antonio Lucacchini	2003	12
10	Characterization and preliminary use of 1-, 2- and 3-methyl-5-phenyl-7-chloro-1,2,3-triazolo[4,5-d]pyrimidine as reaction intermediates Il Farmaco ·Giuliana Biagi,Irene Giorgi,Oreste Livi,Valerio Scartoni,P. L. BARILI	2003	3
11	erythro- and threo-2-Hydroxynonyl substituted 2-phenyladenines and 2-phenyl-8-azaadenines: ligands for A1 adenosine receptors and adenosine deaminase Il Farmaco ·Giuliana Biagi,Irene Giorgi,Oreste Livi,Federica Pacchini,Pietro Rum,Valerio Scartoni,Barbara Costa,Maria Rosa Mazzoni,Laura Giusti	2002	12
12	New 1,2,3-triazolo[1,5-a]quinoxalines: synthesis and binding to benzodiazepine and adenosine receptors. II European Journal of Medicinal Chemistry ·Giuliana Biagi,Irene Giorgi,Oreste Livi,Valerio Scartoni,Laura Betti,Gino Giannaccini,Maria Letizia Trincavelli	2002	65
13	New 5-substituted-1-(2-hydroxybenzoyl)-benzotriazoles, potassium channel activators. IV Il Farmaco ·Giuliana Biagi,Irene Giorgi,Oreste Livi,Valerio Scartoni,P. L. BARILI,Vincenzo Calderone,Enrica Martinotti	2001	20
14	New 2-(2′-phenyl-9′-benzyl-8′-azapurin-6′-ylamino)-carboxylic acid methylesters as ligands for A1 adenosine receptors Il Farmaco ·Giuliana Biagi,Irene Giorgi,Federica Pacchini,Oreste Livi,Valerio Scartoni	2001	4
15	2-Alkyloxyalkylthiohypoxanthines as new potent inhibitors of xanthine oxidase Il Farmaco ·Giuliana Biagi,Irene Giorgi,Federica Pacchini,Oreste Livi,Valerio Scartoni	2001	20
16	Some structural changes on triazolyl-benzotriazoles and triazolyl-benzimidazolones as potential potassium channel activators. III Il Farmaco ·Giuliana Biagi,Vincenzo Calderone,Irene Giorgi,Oreste Livi,Valerio Scartoni,Barbara Baragatti,Enrica Martinotti	2001	28
17	5-(4′-Substituted-2′-nitroanilino)-1,2,3-triazoles as new potential potassium channel activators. I European Journal of Medicinal Chemistry ·Giuliana Biagi,Vincenzo Calderone,Irene Giorgi,Oreste Livi,Valerio Scartoni,Barbara Baragatti,Enrica Martinotti	2000	41
18	Triazolyl–benzimidazolones and triazolyl–benzotriazoles: new potential potassium channel activators. II European Journal of Medicinal Chemistry ·Barbara Baragatti,Giuliana Biagi,Vincenzo Calderone,Irene Giorgi,Oreste Livi,Enrica Martinotti,Valerio Scartoni	2000	27
19	1‐(1,2,3‐triazol‐4‐yl)‐benzimidazolones, a new series of heterocyclic derivatives Journal of Heterocyclic Chemistry ·Lucia Bertelli,Giuliana Biagi,Vincenzo Calderone,Irene Giorgi,Oreste Livi,Valerio Scartoni,P. L. BARILI	2000	8
20	1,2,3-Triazolo[1,5-a][1,4]- and 1,2,3-triazolo[1,5-a][1,5]benzodiazepine derivatives: synthesis and benzodiazepine receptor binding Il Farmaco ·Lucia Bertelli,Giuliana Biagi,Irene Giorgi,Oreste Livi,Clementina Manera,Valerio Scartoni,Claudia Martini,Gino Giannaccini,Maria Letizia Trincavelli,P. L. BARILI	1998	29

About Giuliana Biagi

Giuliana Biagi is a scholar working on Physiology, Organic Chemistry and Toxicology, having authored 46 papers that have together received 683 indexed citations. Recurring topics across this work include Synthesis and Biological Evaluation (26 papers), Synthesis and Characterization of Heterocyclic Compounds (17 papers), Adenosine and Purinergic Signaling (17 papers), Click Chemistry and Applications (12 papers), Synthesis and biological activity (6 papers), Phenothiazines and Benzothiazines Synthesis and Activities (6 papers), Quinazolinone synthesis and applications (5 papers) and Ion channel regulation and function (5 papers). The work is most often cited by research in Physiology (104 citations), Organic Chemistry (527 citations) and Molecular Biology (294 citations). Giuliana Biagi has collaborated with scholars based in Italy and United States. Frequent co-authors include Oreste Livi, Irene Giorgi, Valerio Scartoni, Vincenzo Calderone, Enrica Martinotti, P. L. BARILI, Gino Giannaccini, Laura Betti, Maria Letizia Trincavelli and Clementina Manera. Their work appears in journals such as Journal of Medicinal Chemistry, The Journal of Organic Chemistry and European Journal of Medicinal Chemistry.

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