Ombretta Lenzi

689 total citations
19 papers, 623 citations indexed

About

Ombretta Lenzi is a scholar working on Molecular Biology, Physiology and Organic Chemistry. According to data from OpenAlex, Ombretta Lenzi has authored 19 papers receiving a total of 623 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 13 papers in Physiology and 12 papers in Organic Chemistry. Recurrent topics in Ombretta Lenzi's work include Adenosine and Purinergic Signaling (13 papers), Synthesis and Biological Evaluation (10 papers) and Receptor Mechanisms and Signaling (9 papers). Ombretta Lenzi is often cited by papers focused on Adenosine and Purinergic Signaling (13 papers), Synthesis and Biological Evaluation (10 papers) and Receptor Mechanisms and Signaling (9 papers). Ombretta Lenzi collaborates with scholars based in Italy, Belgium and Denmark. Ombretta Lenzi's co-authors include Vittoria Colotta, Daniela Catarzi, Flavia Varano, Guido Filacchioni, Stefano Moro, Claudia Martini, Maria Letizia Trincavelli, Alessandro Galli, Chiara Costagli and Francesca Deflorian and has published in prestigious journals such as Journal of Medicinal Chemistry, European Journal of Medicinal Chemistry and Bioorganic & Medicinal Chemistry.

In The Last Decade

Ombretta Lenzi

19 papers receiving 615 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ombretta Lenzi Italy 16 402 386 303 64 28 19 623
An‐Hu Li United States 14 501 1.2× 383 1.0× 319 1.1× 69 1.1× 18 0.6× 20 818
Ariel S. Gross United States 10 202 0.5× 424 1.1× 385 1.3× 133 2.1× 25 0.9× 10 609
Miriam de Groote Netherlands 12 274 0.7× 343 0.9× 322 1.1× 97 1.5× 12 0.4× 13 565
Lucia Squarcialupi Italy 16 222 0.6× 244 0.6× 171 0.6× 68 1.1× 11 0.4× 18 424
Regina Link Netherlands 6 181 0.5× 221 0.6× 153 0.5× 56 0.9× 17 0.6× 6 354
Jacobus P. D. van Veldhoven Netherlands 16 177 0.4× 493 1.3× 172 0.6× 132 2.1× 106 3.8× 26 658
Lisa C. W. Chang Netherlands 7 239 0.6× 232 0.6× 185 0.6× 54 0.8× 15 0.5× 7 439
Elisabeth Klaasse Netherlands 10 66 0.2× 223 0.6× 110 0.4× 65 1.0× 92 3.3× 11 374
Joanne Lerpiniere United Kingdom 10 242 0.6× 206 0.5× 89 0.3× 44 0.7× 9 0.3× 11 386
Reynalda de Jesus Switzerland 7 149 0.4× 175 0.5× 70 0.2× 49 0.8× 14 0.5× 8 302

Countries citing papers authored by Ombretta Lenzi

Since Specialization
Citations

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

Fields of papers citing papers by Ombretta Lenzi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ombretta Lenzi

This figure shows the co-authorship network connecting the top 25 collaborators of Ombretta Lenzi. A scholar is included among the top collaborators of Ombretta Lenzi 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 Ombretta Lenzi. Ombretta Lenzi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Mortensen, Martin, Kenneth T. Kongstad, Ombretta Lenzi, et al.. (2019). Developing New 4-PIOL and 4-PHP Analogues for Photoinactivation of γ-Aminobutyric Acid Type A Receptors. ACS Chemical Neuroscience. 10(11). 4669–4684. 6 indexed citations
2.
Lauriola, Maria Michela, et al.. (2012). Allergic Contact Dermatitis From Depilatory Wax. Dermatitis. 23(3). 126–127. 1 indexed citations
3.
Colotta, Vittoria, Ombretta Lenzi, Daniela Catarzi, et al.. (2012). 3-Hydroxy-1H-quinazoline-2,4-dione derivatives as new antagonists at ionotropic glutamate receptors: Molecular modeling and pharmacological studies. European Journal of Medicinal Chemistry. 54. 470–482. 34 indexed citations
4.
Lenzi, Ombretta, Vittoria Colotta, Daniela Catarzi, et al.. (2011). Synthesis, structure–affinity relationships, and molecular modeling studies of novel pyrazolo[3,4-c]quinoline derivatives as adenosine receptor antagonists. Bioorganic & Medicinal Chemistry. 19(12). 3757–3768. 19 indexed citations
6.
7.
Lenzi, Ombretta, Vittoria Colotta, Daniela Catarzi, et al.. (2009). 2-Phenylpyrazolo[4,3-d]pyrimidin-7-one as a New Scaffold To Obtain Potent and Selective Human A3Adenosine Receptor Antagonists: New Insights into the Receptor−Antagonist Recognition. Journal of Medicinal Chemistry. 52(23). 7640–7652. 47 indexed citations
8.
Colotta, Vittoria, Ombretta Lenzi, Daniela Catarzi, et al.. (2008). Novel potent and highly selective human A3 adenosine receptor antagonists belonging to the 4-amido-2-arylpyrazolo[3,4-c]quinoline series: Molecular docking analysis and pharmacological studies. Bioorganic & Medicinal Chemistry. 17(1). 401–410. 19 indexed citations
9.
Colotta, Vittoria, Daniela Catarzi, Flavia Varano, et al.. (2008). Synthesis, ligand–receptor modeling studies and pharmacological evaluation of novel 4-modified-2-aryl-1,2,4-triazolo[4,3-a]quinoxalin-1-one derivatives as potent and selective human A3 adenosine receptor antagonists. Bioorganic & Medicinal Chemistry. 16(11). 6086–6102. 32 indexed citations
10.
Varano, Flavia, Daniela Catarzi, Vittoria Colotta, et al.. (2007). Novel AMPA and kainate receptor antagonists containing the pyrazolo[1,5-c]quinazoline ring system: Synthesis and structure–activity relationships. Bioorganic & Medicinal Chemistry. 16(5). 2617–2626. 28 indexed citations
11.
Colotta, Vittoria, Daniela Catarzi, Flavia Varano, et al.. (2007). New 2-Arylpyrazolo[3,4-c]quinoline Derivatives as Potent and Selective Human A3Adenosine Receptor Antagonists. Synthesis, Pharmacological Evaluation, and Ligand−Receptor Modeling Studies. Journal of Medicinal Chemistry. 50(17). 4061–4074. 50 indexed citations
12.
Lenzi, Ombretta, Daniela Catarzi, Flavia Varano, et al.. (2007). Scouting Human A3 Adenosine Receptor Antagonist Binding Mode Using a Molecular Simplification Approach: From Triazoloquinoxaline to a Pyrimidine Skeleton as a Key Study. Journal of Medicinal Chemistry. 50(26). 6596–6606. 31 indexed citations
13.
Colotta, Vittoria, Daniela Catarzi, Flavia Varano, et al.. (2006). Structural Investigation of the 7-Chloro-3-hydroxy-1H-quinazoline-2,4-dione Scaffold to Obtain AMPA and Kainate Receptor Selective Antagonists. Synthesis, Pharmacological, and Molecular Modeling Studies. Journal of Medicinal Chemistry. 49(20). 6015–6026. 44 indexed citations
14.
Lenzi, Ombretta, Vittoria Colotta, Daniela Catarzi, et al.. (2006). 4-Amido-2-aryl-1,2,4-triazolo[4,3-a]quinoxalin-1-ones as New Potent and Selective Human A3Adenosine Receptor Antagonists. Synthesis, Pharmacological Evaluation, and Ligand−Receptor Modeling Studies. Journal of Medicinal Chemistry. 49(13). 3916–3925. 50 indexed citations
15.
Colotta, Vittoria, Daniela Catarzi, Flavia Varano, et al.. (2005). Synthesis and pharmacological studies at the Gly/NMDA, AMPA and Kainate receptors of new oxazolo[4,5-c]quinolin-4-one derivatives bearing different substituents at position-2 and on the fused benzo ring. European Journal of Medicinal Chemistry. 40(9). 897–907. 25 indexed citations
16.
Varano, Flavia, Daniela Catarzi, Vittoria Colotta, et al.. (2005). 1-Substituted pyrazolo[1,5-c]quinazolines as novel Gly/NMDA receptor antagonists: Synthesis, biological evaluation, and molecular modeling study. Bioorganic & Medicinal Chemistry. 13(19). 5536–5549. 62 indexed citations
18.
19.
Catarzi, Daniela, Vittoria Colotta, Flavia Varano, et al.. (2004). 2-Aryl-8-chloro-1,2,4-triazolo[1,5-a]quinoxalin-4-amines as highly potent A1 and A3 adenosine receptor antagonists. Bioorganic & Medicinal Chemistry. 13(3). 705–715. 29 indexed citations

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