John C. Lukesh

664 total citations
26 papers, 516 citations indexed

About

John C. Lukesh is a scholar working on Biochemistry, Organic Chemistry and Molecular Biology. According to data from OpenAlex, John C. Lukesh has authored 26 papers receiving a total of 516 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Biochemistry, 13 papers in Organic Chemistry and 10 papers in Molecular Biology. Recurrent topics in John C. Lukesh's work include Sulfur Compounds in Biology (15 papers), Sulfur-Based Synthesis Techniques (7 papers) and Redox biology and oxidative stress (4 papers). John C. Lukesh is often cited by papers focused on Sulfur Compounds in Biology (15 papers), Sulfur-Based Synthesis Techniques (7 papers) and Redox biology and oxidative stress (4 papers). John C. Lukesh collaborates with scholars based in United States. John C. Lukesh's co-authors include Ronald T. Raines, Michael J. Palte, Brett VanVeller, Dale L. Boger, Ian W. Windsor, Brian Gold, Katrina T. Forest, Heather M. Brown, Oliver Allemann and Daniel W. Carney and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Angewandte Chemie International Edition.

In The Last Decade

John C. Lukesh

25 papers receiving 513 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
John C. Lukesh United States 15 201 171 160 66 54 26 516
Stéphanie Pèthe France 15 241 1.2× 84 0.5× 201 1.3× 59 0.9× 42 0.8× 24 551
Olivier Duval France 17 326 1.6× 41 0.2× 285 1.8× 52 0.8× 27 0.5× 54 804
Lionel Nauton France 20 421 2.1× 101 0.6× 608 3.8× 97 1.5× 32 0.6× 60 1.0k
Bert‐Jan Baas Netherlands 14 481 2.4× 51 0.3× 330 2.1× 59 0.9× 60 1.1× 24 745
Satish R. Malwal United States 17 336 1.7× 159 0.9× 220 1.4× 76 1.2× 68 1.3× 34 698
Li‐Ming Zhao China 21 293 1.5× 46 0.3× 909 5.7× 102 1.5× 45 0.8× 82 1.3k
Qian‐Qian Yang China 15 243 1.2× 63 0.4× 409 2.6× 41 0.6× 47 0.9× 40 700
M. Srinivasan India 16 287 1.4× 40 0.2× 324 2.0× 29 0.4× 26 0.5× 37 696
Mingzhi Su China 14 227 1.1× 23 0.1× 144 0.9× 25 0.4× 24 0.4× 40 609
M.J. Alcaraz Spain 12 180 0.9× 26 0.2× 187 1.2× 29 0.4× 22 0.4× 17 573

Countries citing papers authored by John C. Lukesh

Since Specialization
Citations

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

Fields of papers citing papers by John C. Lukesh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John C. Lukesh. 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 John C. Lukesh. The network helps show where John C. Lukesh may publish in the future.

Co-authorship network of co-authors of John C. Lukesh

This figure shows the co-authorship network connecting the top 25 collaborators of John C. Lukesh. A scholar is included among the top collaborators of John C. Lukesh 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 John C. Lukesh. John C. Lukesh 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.
Lukesh, John C., et al.. (2025). Self-Reporting H2S Donors: Integrating H2S Release with Real-Time Fluorescence Detection. Chemistry. 7(4). 116–116.
2.
Lukesh, John C., et al.. (2024). An Examination of Chemical Tools for Hydrogen Selenide Donation and Detection. Molecules. 29(16). 3863–3863. 2 indexed citations
3.
Chen, Chen, et al.. (2024). Esterase-Activated Hydrogen Sulfide Donors with Self-Reporting Fluorescence Properties and Highly Tunable Rates of Delivery. ACS Chemical Biology. 19(9). 1910–1917. 4 indexed citations
4.
Lukesh, John C., et al.. (2023). H2S Donors with Cytoprotective Effects in Models of MI/R Injury and Chemotherapy-Induced Cardiotoxicity. Antioxidants. 12(3). 650–650. 19 indexed citations
5.
Marrs, Glen S., et al.. (2023). An ROS-Responsive Donor That Self-Reports Its H2S Delivery by Forming a Benzoxazole-Based Fluorophore. Journal of the American Chemical Society. 145(46). 25486–25494. 18 indexed citations
6.
Yammani, Rama D., et al.. (2022). Mitigation of doxorubicin-induced cardiotoxicity with an H2O2-Activated, H2S-Donating hybrid prodrug. Redox Biology. 53. 102338–102338. 16 indexed citations
7.
Day, Cynthia S., et al.. (2022). Arylselenyl Radical-Mediated Cyclization of N-(2-Alkynyl)anilines: Access to 3-Selenylquinolines. The Journal of Organic Chemistry. 87(13). 8390–8395. 10 indexed citations
8.
Lukesh, John C., et al.. (2022). Intramolecular Thiol‐ and Selenol‐Assisted Delivery of Hydrogen Sulfide. Angewandte Chemie International Edition. 61(45). e202210754–e202210754. 18 indexed citations
9.
Lukesh, John C., et al.. (2021). Illuminating and alleviating cellular oxidative stress with an ROS-activated, H2S-donating theranostic. Tetrahedron Letters. 69. 152944–152944. 13 indexed citations
10.
Lukesh, John C., et al.. (2020). An Innovative Hydrogen Peroxide‐Sensing Scaffold and Insight Towards its Potential as an ROS‐Activated Persulfide Donor. Angewandte Chemie International Edition. 59(49). 22238–22245. 36 indexed citations
11.
Lukesh, John C., et al.. (2020). An Innovative Hydrogen Peroxide‐Sensing Scaffold and Insight Towards its Potential as an ROS‐Activated Persulfide Donor. Angewandte Chemie. 132(49). 22422–22429. 5 indexed citations
12.
Brown, Heather M., et al.. (2019). Highly selective staining and quantification of intracellular lipid droplets with a compact push–pull fluorophore based on benzothiadiazole. Organic & Biomolecular Chemistry. 18(3). 495–499. 24 indexed citations
13.
Lukesh, John C., Daniel W. Carney, Huijun Dong, et al.. (2017). Vinblastine 20′ Amides: Synthetic Analogues That Maintain or Improve Potency and Simultaneously Overcome Pgp-Derived Efflux and Resistance. Journal of Medicinal Chemistry. 60(17). 7591–7604. 15 indexed citations
14.
Yang, Shouliang, et al.. (2016). Total synthesis of a key series of vinblastines modified at C4 that define the importance and surprising trends in activity. Chemical Science. 8(2). 1560–1569. 17 indexed citations
15.
Lukesh, John C., et al.. (2014). Pyrazine-derived disulfide-reducing agent for chemical biology. Chemical Communications. 50(67). 9591–9591. 11 indexed citations
16.
Lukesh, John C., et al.. (2014). Organocatalysts of oxidative protein folding inspired by protein disulfide isomerase. Organic & Biomolecular Chemistry. 12(43). 8598–8602. 14 indexed citations
17.
Lukesh, John C., Brett VanVeller, & Ronald T. Raines. (2013). Thiols and Selenols as Electron‐Relay Catalysts for Disulfide‐Bond Reduction. Angewandte Chemie International Edition. 52(49). 12901–12904. 33 indexed citations
18.
Lukesh, John C., Brett VanVeller, & Ronald T. Raines. (2013). Thiols and Selenols as Electron‐Relay Catalysts for Disulfide‐Bond Reduction. Angewandte Chemie. 125(49). 13139–13142. 11 indexed citations
19.
Lukesh, John C., Brett VanVeller, & Ronald T. Raines. (2013). Innentitelbild: Thiols and Selenols as Electron‐Relay Catalysts for Disulfide‐Bond Reduction (Angew. Chem. 49/2013). Angewandte Chemie. 125(49). 12982–12982. 1 indexed citations
20.
Lukesh, John C., Michael J. Palte, & Ronald T. Raines. (2012). A Potent, Versatile Disulfide-Reducing Agent from Aspartic Acid. Journal of the American Chemical Society. 134(9). 4057–4059. 117 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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