С. Г. Полоник

631 total citations
54 papers, 491 citations indexed

About

С. Г. Полоник is a scholar working on Toxicology, Organic Chemistry and Molecular Biology. According to data from OpenAlex, С. Г. Полоник has authored 54 papers receiving a total of 491 indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Toxicology, 34 papers in Organic Chemistry and 18 papers in Molecular Biology. Recurrent topics in С. Г. Полоник's work include Bioactive Compounds and Antitumor Agents (36 papers), Synthesis and biological activity (11 papers) and Synthesis and Reactions of Organic Compounds (10 papers). С. Г. Полоник is often cited by papers focused on Bioactive Compounds and Antitumor Agents (36 papers), Synthesis and biological activity (11 papers) and Synthesis and Reactions of Organic Compounds (10 papers). С. Г. Полоник collaborates with scholars based in Russia, Taiwan and United States. С. Г. Полоник's co-authors include Dmitry L. Aminin, Irina V. Guzhova, Boris A. Margulis, В. А. Денисенко, N. I. Uvarova, В. Ф. Ануфриев, Vladimir F. Lazarev, Evgeny Nudler, Elena R. Mikhaylova and Alexander Tolkach and has published in prestigious journals such as SHILAP Revista de lepidopterología, Biochemical and Biophysical Research Communications and International Journal of Molecular Sciences.

In The Last Decade

С. Г. Полоник

53 papers receiving 480 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
С. Г. Полоник Russia 11 270 204 203 78 38 54 491
Neil Frankish Ireland 13 39 0.1× 141 0.7× 192 0.9× 51 0.7× 13 0.3× 33 666
Ojas A. Namjoshi United States 20 53 0.2× 577 2.8× 396 2.0× 24 0.3× 9 0.2× 46 1.1k
Patricia A. Rose Canada 15 43 0.2× 183 0.9× 328 1.6× 12 0.2× 13 0.3× 45 1.2k
Chihiro Ito Japan 15 58 0.2× 147 0.7× 238 1.2× 26 0.3× 18 0.5× 46 661
Ekaterina S. Menchinskaya Russia 16 51 0.2× 106 0.5× 254 1.3× 26 0.3× 356 9.4× 71 760
Jae Wook Lee South Korea 15 24 0.1× 121 0.6× 330 1.6× 27 0.3× 16 0.4× 47 624
Nobuko Nishimura United States 14 33 0.1× 224 1.1× 124 0.6× 43 0.6× 22 0.6× 17 491
Michael A. Ernst‐Russell United States 7 29 0.1× 122 0.6× 166 0.8× 8 0.1× 62 1.6× 11 396
Ana Elisa Gonçalves Brazil 9 19 0.1× 228 1.1× 158 0.8× 40 0.5× 6 0.2× 11 446
Xian‐Qing Deng China 23 40 0.1× 959 4.7× 885 4.4× 12 0.2× 14 0.4× 73 1.7k

Countries citing papers authored by С. Г. Полоник

Since Specialization
Citations

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

Fields of papers citing papers by С. Г. Полоник

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by С. Г. Полоник. 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 С. Г. Полоник. The network helps show where С. Г. Полоник may publish in the future.

Co-authorship network of co-authors of С. Г. Полоник

This figure shows the co-authorship network connecting the top 25 collaborators of С. Г. Полоник. A scholar is included among the top collaborators of С. Г. Полоник 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 С. Г. Полоник. С. Г. Полоник 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.
Агафонова, И. Г., Ekaterina A. Chingizova, Ekaterina S. Menchinskaya, et al.. (2024). Protection Activity of 1,4-Naphthoquinones in Rotenone-Induced Models of Neurotoxicity. Marine Drugs. 22(2). 62–62. 3 indexed citations
2.
Pislyagin, Еvgeny А., Ekaterina S. Menchinskaya, Ekaterina A. Chingizova, et al.. (2024). Antinociceptive effect and anti-inflammatory activity of 1,4-naphthoquinones in mice. SHILAP Revista de lepidopterología. 39–50. 3 indexed citations
3.
Pislyagin, Еvgeny А., Ekaterina S. Menchinskaya, Ekaterina A. Chingizova, et al.. (2023). Anti-Inflammatory Activity of 1,4-Naphthoquinones Blocking P2X7 Purinergic Receptors in RAW 264.7 Macrophage Cells. Toxins. 15(1). 47–47. 18 indexed citations
4.
Pislyagin, Еvgeny А., Ekaterina S. Menchinskaya, Ekaterina A. Chingizova, et al.. (2023). Tetracyclic 1,4-Naphthoquinone Thioglucoside Conjugate U-556 Blocks the Purinergic P2X7 Receptor in Macrophages and Exhibits Anti-Inflammatory Activity In Vivo. International Journal of Molecular Sciences. 24(15). 12370–12370. 4 indexed citations
5.
Komarova, Elena Y., Dmitry Alexeev, Sergey Efremov, et al.. (2021). Prevention of High Glucose-Mediated EMT by Inhibition of Hsp70 Chaperone. International Journal of Molecular Sciences. 22(13). 6902–6902. 11 indexed citations
6.
Fedorov, Sergey N., et al.. (2021). Synthesis and studies of acetylthioglycoside conjugates of 4-chloro-1,2-dithiole-3-thione as potential antitumor agents. Russian Chemical Bulletin. 70(3). 573–579. 2 indexed citations
7.
8.
Полоник, С. Г., et al.. (2020). Оценка эффективности превентивной терапии с индуктором шаперонов U133 в модели доклинической стадии болезни Паркинсона у пожилых крыс. Российский физиологический журнал им  И  М  Сеченова. 106(10). 1251–1265. 2 indexed citations
9.
Pislyagin, Еvgeny А., Ekaterina S. Menchinskaya, Ekaterina A. Chingizova, et al.. (2020). Synthetic 1,4-Naphthoquinones inhibit P2X7 receptors in murine neuroblastoma cells. Bioorganic & Medicinal Chemistry. 31. 115975–115975. 17 indexed citations
10.
Полоник, С. Г., et al.. (2019). Synthesis and Screening of Anti-HSV-1 Activity of Thioglucoside Derivatives of Natural Polyhydroxy-1,4-Naphthoquinones. Natural Product Communications. 14(6). 4 indexed citations
11.
Semenova, Marina N., Ekaterina A. Yurchenko, В. А. Денисенко, et al.. (2017). Synthesis and Comparative Evaluation of Polymethoxy Substituted 1,4-Naphthoquinones and their Acetyl-O-glucosides as Cytotoxic Agents. Natural Product Communications. 12(7). 2 indexed citations
12.
Полоник, С. Г., et al.. (2016). DMSO-mediated transformation of 3-amino-2-hydroxynaphthazarins to natural 2,3-dihydroxynaphthazarins and related compounds. Tetrahedron Letters. 57(30). 3303–3306. 6 indexed citations
13.
Lazarev, Vladimir F., et al.. (2011). Kinetics of chaperone activity of proteins Hsp70 and Hdj1 in human leukemia U-937 cells after preconditioning with thermal shock or compound U-133. Biochemistry (Moscow). 76(5). 590–595. 18 indexed citations
14.
15.
Полоник, С. Г. & В. А. Денисенко. (2009). Synthesis and properties of fused tetracyclic derivatives of 1,4-naphthoquinone thioglycosides. Russian Chemical Bulletin. 58(5). 1062–1066. 6 indexed citations
16.
Полоник, С. Г.. (2009). Glycosylation of Shikonin by the Helferich method. Chemistry of Natural Compounds. 45(2). 247–248. 4 indexed citations
17.
Полоник, С. Г., et al.. (2006). Reductive heterocyclization of 2,2-dichloro-1,4-naphthoquinone into naphtho[2,3-f][1,2,3,4,5]pentathiepine-6,11-diol under the action of sodium hydrosulfide in DMF. Russian Journal of Organic Chemistry. 42(2). 302–303. 3 indexed citations
18.
Полоник, С. Г., Alexander Tolkach, & N. I. Uvarova. (1996). ChemInform Abstract: Reaction of Acetylated 1,4‐Naphthoquinone Thioglycosides with Nucleophilic Reagents.. ChemInform. 27(29). 1 indexed citations
19.
Полоник, С. Г., et al.. (1992). Synthesis of acetylated glycosides of hydroxyjuglones and study of their antifungal activity. Pharmaceutical Chemistry Journal. 26(6). 500–502. 8 indexed citations
20.
Полоник, С. Г., Н. Д. Похило, В. И. Баранов, & N. I. Uvarova. (1977). Quantitative determination of triterpenoids of the dammarane series by the densitometry of thin-layer chromatograms. Chemistry of Natural Compounds. 13(3). 297–300. 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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