Lennart Bunch
About
Lennart Bunch is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Organic Chemistry.
According to data from OpenAlex, Lennart Bunch has authored 80 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 60 papers in Molecular Biology, 54 papers in Cellular and Molecular Neuroscience and 22 papers in Organic Chemistry. Recurrent topics in Lennart Bunch's work include Neuroscience and Neuropharmacology Research (53 papers), Receptor Mechanisms and Signaling (31 papers) and Chemical Synthesis and Analysis (24 papers). Lennart Bunch is often cited by papers focused on Neuroscience and Neuropharmacology Research (53 papers), Receptor Mechanisms and Signaling (31 papers) and Chemical Synthesis and Analysis (24 papers). Lennart Bunch collaborates with scholars based in Denmark, France and United States. Lennart Bunch's co-authors include Charles S. Demmer, Niels Krogsgaard‐Larsen, Anders A. Jensen, Mette N. Erichsen, Birgitte Nielsen, Stine F. Pedersen, Ebbe Boedtkjer, Povl Krogsgaard‐Larsen, Darryl S. Pickering and Michael Kreis and has published in prestigious journals such as Chemical Reviews, Journal of Neuroscience and Journal of Medicinal Chemistry.
In The Last Decade
Lennart Bunch
80 papers receiving 2.3k citations
Hit Papers
Peers
Lennart Bunch
Jesper L. Kristensen Denmark
Vincenzo Tortorella Italy
Robert W. Carling United States
T. G. Murali Dhar United States
Maurizio Anzini Italy
John M. Humphrey United States
John E. Macor United States
Kyoji Furuta Japan
Jing Xu China
Toshiaki Mase Japan
Citations per year, relative to Lennart Bunch Lennart Bunch (= 1×)
peers
Jesper L. Kristensen
Countries citing papers authored by Lennart Bunch
Since
Specialization
Citations
This map shows the geographic impact of Lennart Bunch'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 Lennart Bunch with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Lennart Bunch more than expected).
Fields of papers citing papers by Lennart Bunch
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by Lennart Bunch. 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 Lennart Bunch. The network helps show where Lennart Bunch may publish in the future.
Co-authorship network of co-authors of Lennart Bunch
This figure shows the co-authorship network connecting the top 25 collaborators of Lennart Bunch. A scholar is included among the top collaborators of Lennart Bunch 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 Lennart Bunch. Lennart Bunch is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Liu, Na, Fanny Malhaire, Isabelle Brabet, et al.. (2024). Design, Synthesis, Pharmacology, and In Silico Studies of (1S,2S,3S)-2-((S)-Amino(carboxy)methyl)-3-(carboxymethyl)cyclopropane-1-carboxylic Acid (LBG30300): A Picomolar Potency Subtype-Selective mGlu2 Receptor Agonist. Journal of Medicinal Chemistry. 67(2). 1314–1326.
2.
Liu, Na, et al.. (2024). Synthesis and pharmacological characterization of conformationally restricted 2-amino-Adipic acid analogs and carboxycyclopropyl glycines as selective metabotropic glutamate 2 receptor agonists. European Journal of Medicinal Chemistry. 266. 116157–116157.
3.
Poulie, Christian B. M., Gaël Barthet, Walden E. Bjørn‐Yoshimoto, et al.. (2022). (S)-2-Mercaptohistidine: A First Selective Orthosteric GluK3 Antagonist. ACS Chemical Neuroscience. 13(10). 1580–1587.
4.
Zhao, Fabao, et al.. (2022). Discovery of (R)-2-amino-3-triazolpropanoic acid derivatives as NMDA receptor glycine site agonists with GluN2 subunit-specific activity. Frontiers in Chemistry. 10. 1008233–1008233.
5.
Poulie, Christian B. M., et al.. (2020). A Diversity Oriented Synthesis Approach to New 2,3-trans-Substituted l -Proline Analogs as Potential Ligands for the Ionotropic Glutamate Receptors. ACS Chemical Neuroscience. 11(5). 702–714.
6.
Demmer, Charles S., Floris Chevallier, Thierry Roisnel, et al.. (2018). Functionalization of Oxazolo[4,5‐b]pyrazines by Deprotometallation. European Journal of Organic Chemistry. 2018(29). 3904–3913.
7.
Bunch, Lennart, et al.. (2018). Delineation of the functional properties and the mechanism of action of AA29504, an allosteric agonist and positive allosteric modulator of GABAA receptors. Biochemical Pharmacology. 150. 305–319.
8.
Hansen, Stinne W., Mette N. Erichsen, Tri H. V. Huynh, et al.. (2016). New Insight into the Structure–Activity Relationships of the Selective Excitatory Amino Acid Transporter Subtype 1 (EAAT1) Inhibitors UCPH‐101 and UCPH‐102. ChemMedChem. 11(4). 382–402.
9.
Demmer, Charles S., Charlotte Møller, Patricia M.G.E. Brown, et al.. (2015). Binding Mode of an α-Amino Acid-Linked Quinoxaline-2,3-dione Analogue at Glutamate Receptor Subtype GluK1. ACS Chemical Neuroscience. 6(6). 845–854.
10.
Bader, Benjamin, Corina Ehnert, Christoffer Bundgaard, et al.. (2015). A Multifaceted GABAA Receptor Modulator: Functional Properties and Mechanism of Action of the Sedative-Hypnotic and Recreational Drug Methaqualone (Quaalude). Molecular Pharmacology. 88(2). 401–420.
11.
Jensen, Anders A., Niels F. Jensen, Lennart Bunch, et al.. (2015). The glutamate transport inhibitor DL-Threo-β-Benzyloxyaspartic acid (DL-TBOA) differentially affects SN38- and oxaliplatin-induced death of drug-resistant colorectal cancer cells. BMC Cancer. 15(1). 411–411.
12.
Gynther, Mikko, Aleksanteri Petsalo, Steen Honoré Hansen, Lennart Bunch, & Darryl S. Pickering. (2014). Blood–Brain Barrier Permeability and Brain Uptake Mechanism of Kainic Acid and Dihydrokainic Acid. Neurochemical Research. 40(3). 542–549.
13.
Erichsen, Mette N., Charles S. Demmer, Bjarke Abrahamsen, et al.. (2014). Probing for Improved Potency and In Vivo Bioavailability of Excitatory Amino Acid Transporter Subtype 1 Inhibitors UCPH-101 and UCPH-102: Design, Synthesis and Pharmacological Evaluation of Substituted 7-Biphenyl Analogs. Neurochemical Research. 39(10). 1964–1979.
14.
Demmer, Charles S. & Lennart Bunch. (2014). Benzoxazoles and oxazolopyridines in medicinal chemistry studies. European Journal of Medicinal Chemistry. 97. 778–785.
15.
Abrahamsen, Bjarke, Nicole Schneider, Mette N. Erichsen, et al.. (2013). Allosteric Modulation of an Excitatory Amino Acid Transporter: The Subtype-Selective Inhibitor UCPH-101 Exerts Sustained Inhibition of EAAT1 through an Intramonomeric Site in the Trimerization Domain. Journal of Neuroscience. 33(3). 1068–1087.
16.
Boedtkjer, Ebbe, Lennart Bunch, & Stine F. Pedersen. (2012). Physiology, Pharmacology and Pathophysiology of the pH Regulatory Transport Proteins NHE1 and NBCn1: Similarities, Differences, and Implications for Cancer Therapy. Current Pharmaceutical Design. 18(10). 1345–1371.
17.
Vogensen, Stine B., Jeremy R. Greenwood, Lennart Bunch, & Rasmus P. Clausen. (2011). Glutamate Receptor Agonists: Stereochemical Aspects. Current Topics in Medicinal Chemistry. 11(7). 887–906.
18.
Bunch, Lennart, Darryl S. Pickering, Thierry Gefflaut, et al.. (2009). 4,4‐Dimethyl‐ and Diastereomeric 4‐Hydroxy‐4‐methyl‐ (2S)‐Glutamate Analogues Display Distinct Pharmacological Profiles at Ionotropic Glutamate Receptors and Excitatory Amino Acid Transporters. ChemMedChem. 4(11). 1925–1929.
19.
Bunch, Lennart & Povl Krogsgaard‐Larsen. (2008). Subtype selective kainic acid receptor agonists: Discovery and approaches to rational design. Medicinal Research Reviews. 29(1). 3–28.
20.
Hermit, Mette B., Jeremy R. Greenwood, Birgitte Nielsen, et al.. (2004). Ibotenic acid and thioibotenic acid: a remarkable difference in activity at group III metabotropic glutamate receptors. European Journal of Pharmacology. 486(3). 241–250.
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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