И. В. Серков

646 total citations
60 papers, 537 citations indexed

About

И. В. Серков is a scholar working on Organic Chemistry, Pharmacology and Computational Theory and Mathematics. According to data from OpenAlex, И. В. Серков has authored 60 papers receiving a total of 537 indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Organic Chemistry, 28 papers in Pharmacology and 17 papers in Computational Theory and Mathematics. Recurrent topics in И. В. Серков's work include Cholinesterase and Neurodegenerative Diseases (21 papers), Synthesis and biological activity (19 papers) and Computational Drug Discovery Methods (17 papers). И. В. Серков is often cited by papers focused on Cholinesterase and Neurodegenerative Diseases (21 papers), Synthesis and biological activity (19 papers) and Computational Drug Discovery Methods (17 papers). И. В. Серков collaborates with scholars based in Russia, United States and Czechia. И. В. Серков's co-authors include Alexey N. Proshin, Галина Ф. Махаева, Natalia P. Boltneva, С. О. Бачурин, N. V. Kovaleva, Sofya V. Lushchekina, Елена В. Рудакова, Rudy J. Richardson, В. В. Безуглов and С. О. Бачурин and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Medicinal Chemistry and Molecules.

In The Last Decade

И. В. Серков

57 papers receiving 533 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
И. В. Серков Russia 12 319 298 228 139 35 60 537
Hongzhi Lin China 13 394 1.2× 238 0.8× 162 0.7× 255 1.8× 64 1.8× 15 731
X. Formosa Spain 9 321 1.0× 479 1.6× 361 1.6× 143 1.0× 141 4.0× 10 636
A. Altan Bilgin Türkiye 9 715 2.2× 200 0.7× 136 0.6× 131 0.9× 14 0.4× 15 856
Zvetanka Zhivkova Bulgaria 14 156 0.5× 143 0.5× 134 0.6× 222 1.6× 18 0.5× 29 482
Elena Gómez Spain 15 439 1.4× 263 0.9× 202 0.9× 192 1.4× 77 2.2× 40 690
Evgeny V. Shchegolkov Russia 15 514 1.6× 181 0.6× 130 0.6× 100 0.7× 11 0.3× 66 655
Slávka Hamuľaková Slovakia 14 287 0.9× 302 1.0× 218 1.0× 224 1.6× 85 2.4× 25 567
Kamilia M. Amin Egypt 15 673 2.1× 155 0.5× 77 0.3× 273 2.0× 18 0.5× 26 844
Jane L. Wang United States 10 310 1.0× 260 0.9× 95 0.4× 121 0.9× 16 0.5× 10 535
Yasinalli Tamboli India 14 224 0.7× 62 0.2× 78 0.3× 201 1.4× 20 0.6× 35 469

Countries citing papers authored by И. В. Серков

Since Specialization
Citations

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

Fields of papers citing papers by И. В. Серков

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by И. В. Серков. 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 И. В. Серков. The network helps show where И. В. Серков may publish in the future.

Co-authorship network of co-authors of И. В. Серков

This figure shows the co-authorship network connecting the top 25 collaborators of И. В. Серков. A scholar is included among the top collaborators of И. В. Серков 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 И. В. Серков. И. В. Серков 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.
Махаева, Галина Ф., N. V. Kovaleva, Елена В. Рудакова, et al.. (2024). Combining Experimental and Computational Methods to Produce Conjugates of Anticholinesterase and Antioxidant Pharmacophores with Linker Chemistries Affecting Biological Activities Related to Treatment of Alzheimer’s Disease. Molecules. 29(2). 321–321. 11 indexed citations
2.
Proshin, Alexey N., Т. П. Трофимова, O. N. Zefirova, et al.. (2024). New 1,1-dibenzyl-3-(1-benzyl-1H-pyrazol-4-yl)-2-methylisothioureas: synthesis and evaluation of antioxidant activity. Russian Chemical Bulletin. 73(5). 1399–1407.
3.
Серков, И. В., Alexey N. Proshin, N. V. Kovaleva, et al.. (2023). Synthesis and properties of new derivatives of 4-amino-2,3-polymethylenequinolines with antioxidant function. Russian Chemical Bulletin. 72(3). 802–806. 6 indexed citations
4.
Махаева, Галина Ф., N. V. Kovaleva, Natalia P. Boltneva, et al.. (2022). Bis-Amiridines as Acetylcholinesterase and Butyrylcholinesterase Inhibitors: N-Functionalization Determines the Multitarget Anti-Alzheimer’s Activity Profile. Molecules. 27(3). 1060–1060. 19 indexed citations
5.
Серков, И. В., et al.. (2022). Phenothiazine derivatives containing a NO-generating fragment. Russian Chemical Bulletin. 71(12). 2757–2760. 2 indexed citations
6.
Серков, И. В., Alexey N. Proshin, N. V. Kovaleva, et al.. (2022). Tacrine Derivatives Containing an Antioxidant Moiety. Doklady Chemistry. 506(1). 190–195. 2 indexed citations
7.
Махаева, Галина Ф., Sofya V. Lushchekina, N. V. Kovaleva, et al.. (2021). Amiridine-piperazine hybrids as cholinesterase inhibitors and potential multitarget agents for Alzheimer's disease treatment. Bioorganic Chemistry. 112. 104974–104974. 39 indexed citations
8.
Махаева, Галина Ф., N. V. Kovaleva, Елена В. Рудакова, et al.. (2020). New Multifunctional Agents Based on Conjugates of 4-Amino-2,3-polymethylenequinoline and Butylated Hydroxytoluene for Alzheimer’s Disease Treatment. Molecules. 25(24). 5891–5891. 38 indexed citations
9.
Махаева, Галина Ф., N. V. Kovaleva, Natalia P. Boltneva, et al.. (2020). New Hybrids of 4-Amino-2,3-polymethylene-quinoline and p-Tolylsulfonamide as Dual Inhibitors of Acetyl- and Butyrylcholinesterase and Potential Multifunctional Agents for Alzheimer’s Disease Treatment. Molecules. 25(17). 3915–3915. 37 indexed citations
10.
Серков, И. В., et al.. (2020). FIBRO-ADIPOSE VASCULAR ANOMALY IS A NEW DIAGNOSIS IN THE PRACTICE OF A PEDIATRIC VASCULAR SURGEON. EXPERIENCE IN DIAGNOSTICS AND TREATMENT. Russian Journal of Pediatric Surgery. 24(1). 11–15.
11.
Gretskaya, N. M., Roman Akasov, S. V. Burov, et al.. (2020). Novel bexarotene derivatives: Synthesis and cytotoxicity evaluation for glioma cells in 2D and 3D in vitro models. European Journal of Pharmacology. 883. 173346–173346. 10 indexed citations
12.
Akimov, Mikhail, Denis S. Kudryavtsev, N. M. Gretskaya, et al.. (2020). Arachidonoylcholine and Other Unsaturated Long-Chain Acylcholines Are Endogenous Modulators of the Acetylcholine Signaling System. Biomolecules. 10(2). 283–283. 28 indexed citations
13.
Махаева, Галина Ф., N. V. Kovaleva, Natalia P. Boltneva, et al.. (2019). Conjugates of tacrine and 1,2,4-thiadiazole derivatives as new potential multifunctional agents for Alzheimer’s disease treatment: Synthesis, quantum-chemical characterization, molecular docking, and biological evaluation. Bioorganic Chemistry. 94. 103387–103387. 55 indexed citations
14.
Brito, Alex, et al.. (2018). Rabbit plasma metabolomic analysis of Nitroproston®: a multi target natural prostaglandin based-drug. Metabolomics. 14(9). 112–112. 5 indexed citations
15.
16.
Неганова, Маргарита Е., et al.. (2016). N,N’-Substituted Selenoureas as Polyfunctional Antioxidants. Bulletin of Experimental Biology and Medicine. 160(3). 340–342. 4 indexed citations
17.
Махаева, Галина Ф., Natalia P. Boltneva, Sofya V. Lushchekina, et al.. (2016). Synthesis, molecular docking and biological evaluation of N,N-disubstituted 2-aminothiazolines as a new class of butyrylcholinesterase and carboxylesterase inhibitors. Bioorganic & Medicinal Chemistry. 24(5). 1050–1062. 55 indexed citations
18.
Серков, И. В., Alexey N. Proshin, N. V. Kovaleva, et al.. (2016). Synthesis of γ-carbolines containing NO-donor fragment and assessment of their anticholinesterase activity. Russian Chemical Bulletin. 65(11). 2718–2721. 4 indexed citations
19.
Grigoriev, V. V., et al.. (2010). Influence of derivatives of arachidonic and docosohexaenic acids on AMPA receptors in Purkinje neurons and cognitive functions in mice. Biology Bulletin. 37(3). 312–315. 2 indexed citations
20.
Серков, И. В., E. F. Shevtsova, E. G. Kireeva, et al.. (2007). Interaction of docosahexaenoic acid derivatives with mitochondria. Doklady Biological Sciences. 414(1). 187–189. 5 indexed citations

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