Peter Kutschy

1.3k total citations
81 papers, 1.1k citations indexed

About

Peter Kutschy is a scholar working on Organic Chemistry, Molecular Biology and Toxicology. According to data from OpenAlex, Peter Kutschy has authored 81 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 53 papers in Organic Chemistry, 46 papers in Molecular Biology and 14 papers in Toxicology. Recurrent topics in Peter Kutschy's work include Genomics, phytochemicals, and oxidative stress (31 papers), Synthesis and biological activity (16 papers) and Synthesis and Reactivity of Sulfur-Containing Compounds (15 papers). Peter Kutschy is often cited by papers focused on Genomics, phytochemicals, and oxidative stress (31 papers), Synthesis and biological activity (16 papers) and Synthesis and Reactivity of Sulfur-Containing Compounds (15 papers). Peter Kutschy collaborates with scholars based in Slovakia, Japan and United States. Peter Kutschy's co-authors include Milan Dzurilla, Roman Mezencev, Mojmı́r Suchý, Kenji Monde, Mitsuo Takasugi, Martina Bago Pilátová, Nobuyuki Harada, Ján Mojžíš, Mariana Budovská and Eva Balentová and has published in prestigious journals such as The Journal of Organic Chemistry, Journal of Chromatography A and Tetrahedron.

In The Last Decade

Peter Kutschy

74 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peter Kutschy Slovakia 19 573 547 211 162 155 81 1.1k
Gábor Tóth Hungary 21 761 1.3× 386 0.7× 221 1.0× 67 0.4× 66 0.4× 135 1.3k
Genrikh A. Tolstikov Russia 21 579 1.0× 516 0.9× 70 0.3× 58 0.4× 112 0.7× 83 1.1k
Kim Messer Germany 16 525 0.9× 259 0.5× 250 1.2× 51 0.3× 74 0.5× 21 782
Alka Kurup United States 19 470 0.8× 390 0.7× 139 0.7× 52 0.3× 34 0.2× 32 1.1k
Hermann Lotter Germany 20 378 0.7× 538 1.0× 62 0.3× 74 0.5× 266 1.7× 78 1.2k
Milan Dzurilla Slovakia 11 373 0.7× 222 0.4× 90 0.4× 63 0.4× 65 0.4× 52 571
P. Rodighiero Italy 19 553 1.0× 342 0.6× 81 0.4× 225 1.4× 315 2.0× 91 1.0k
Nobuyuki Harada Japan 17 574 1.0× 452 0.8× 396 1.9× 42 0.3× 155 1.0× 26 1.3k
M Plat France 18 610 1.1× 323 0.6× 86 0.4× 43 0.3× 102 0.7× 83 1.1k
Magoichi Sako Japan 16 418 0.7× 458 0.8× 45 0.2× 64 0.4× 66 0.4× 107 920

Countries citing papers authored by Peter Kutschy

Since Specialization
Citations

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

Fields of papers citing papers by Peter Kutschy

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Peter Kutschy

This figure shows the co-authorship network connecting the top 25 collaborators of Peter Kutschy. A scholar is included among the top collaborators of Peter Kutschy 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 Peter Kutschy. Peter Kutschy 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.
Pilátová, Martina Bago, Peter Kutschy, Lenka Varinská, et al.. (2013). In vitro toxicity of camalexin derivatives in human cancer and non-cancer cells. Toxicology in Vitro. 27(2). 939–944. 20 indexed citations
2.
Kutschy, Peter, et al.. (2013). Spirocyclisation of phytoalexin 1-methoxybrassinin in the presence of Grignard reagents. Chemical Papers. 67(6). 3 indexed citations
3.
Gondová, Taťána, et al.. (2012). Stereoselective separation of spiroindoline phytoalexins on R-naphthylethyl cyclofructan 6-based chiral stationary phase. Journal of Chromatography A. 1272. 100–105. 20 indexed citations
4.
Mezencev, Roman, et al.. (2011). Camalexin induces apoptosis in T-leukemia Jurkat cells by increased concentration of reactive oxygen species and activation of caspase-8 and caspase-9. Journal of Natural Medicines. 65(3-4). 488–499. 34 indexed citations
5.
Mezencev, Roman, Peter Kutschy, Aneta Salayová, Taylor B. Updegrove, & Jane McDonald. (2009). The design, synthesis and anticancer activity of new nitrogen mustard derivatives of natural indole phytoalexin 1-methoxyspirobrassinol. Neoplasma. 56(4). 321–330. 14 indexed citations
6.
Kutschy, Peter, Aneta Salayová, Tibor Kožár, et al.. (2009). 2-(Substituted phenyl)amino analogs of 1-methoxyspirobrassinol methyl ether: Synthesis and anticancer activity. Bioorganic & Medicinal Chemistry. 17(10). 3698–3712. 37 indexed citations
7.
Mezencev, Roman, Melina Galizzi, Peter Kutschy, & Roberto Docampo. (2009). Trypanosoma cruzi: Antiproliferative effect of indole phytoalexins on intracellular amastigotes in vitro. Experimental Parasitology. 122(1). 66–69. 39 indexed citations
8.
Mezencev, Roman, Peter Kutschy, Aneta Salayová, et al.. (2008). Anticancer Properties of 2-Piperidyl Analogues of the Natural Indole Phytoalexin 1-Methoxyspirobrassinol. Chemotherapy. 54(5). 372–378. 28 indexed citations
9.
Bekešová, Slávka, et al.. (2005). ESI-ion trap multistage and MALDI-TOF mass spectrometry study of protonated per-O-acetyl indole glucosides. Chemia Analityczna. 50(1). 223–233.
10.
Monde, Kenji, Tohru Taniguchi, Nobuaki Miura, et al.. (2005). Chiral cruciferous phytoalexins: Preparation, absolute configuration, and biological activity. Bioorganic & Medicinal Chemistry. 13(17). 5206–5212. 44 indexed citations
11.
Humeník, Martin, Peter Kutschy, Vladimı́r Kováčik, & Slávka Bekešová. (2005). 1,2-Anhydrosaccharides and 1,2-Cyclic Sulfites as Saccharide Donors in Convergent Synthesis of Glucopyranosyl-, Mannopyranosyl- and Ribofuranosylbenzocamalexin. Collection of Czechoslovak Chemical Communications. 70(4). 487–506. 6 indexed citations
12.
13.
Kutschy, Peter, Mojmı́r Suchý, Aldo Andreani, et al.. (2002). A new approach to the synthesis of rare thiazino[6,5-b]indol-4-one derivatives. First total synthesis of the indole phytoalexin cyclobrassinon. Tetrahedron. 58(44). 9029–9039. 19 indexed citations
14.
Dzurilla, Milan, et al.. (2001). Synthesis of Camalexin. Molecules. 6(9). 716–720. 10 indexed citations
15.
Kutschy, Peter, et al.. (2000). Cytotoxic effect of cruciferous phytoalexins against murine L1210 leukemia and B16 melanoma.. 55(6). 701–707. 16 indexed citations
16.
Monde, Kenji, Nobuyuki Harada, Mitsuo Takasugi, et al.. (2000). Enantiomeric Excess of a Cruciferous Phytoalexin, Spirobrassinin, and Its Enantiomeric Enrichment in an Achiral HPLC System. Journal of Natural Products. 63(9). 1312–1314. 34 indexed citations
17.
Iddon, Brian, Peter Kutschy, Andrew Robinson, et al.. (1992). 2H-benzimidazoles (isobenzimidazoles). Part 7. A new route to triclabendazole [5-chloro-6-(2,3-dichlorophenoxy)-2-methylthio-1H-benzimidazole] and congeneric benzimidazoles. Journal of the Chemical Society Perkin Transactions 1. 3129–3129. 13 indexed citations
18.
Dzurilla, Milan, et al.. (1987). Synthesis of 1,3-diazaspiro[5,5]undecanes and 1-thia-3-azaspiro[5,5]undec-2-enes by reaction of 2-cyanocyclohexylideneacetyl isothiocyanate with amines and sodium hydrogen sulfide. Collection of Czechoslovak Chemical Communications. 52(4). 989–994. 1 indexed citations
19.
Dzurilla, Milan, Peter Kutschy, & Pavol Kristián. (1985). Boron Trifluoride-Catalyzed Cyclization ofN-Substituted-N′-(3-substituted propenoyl)-thioureas: A New Synthesis of 1,3-Thiazines. Synthesis. 1985(10). 933–934. 11 indexed citations
20.
Dzurilla, Milan, Pavol Kristián, & Peter Kutschy. (1977). Reactions of α-substituted cinnamoyl isothiocyanates with sodium hydrosulphide and diazomethane. Collection of Czechoslovak Chemical Communications. 42(10). 2938–2944. 2 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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