Mikhail V. Pugachev

461 total citations
26 papers, 347 citations indexed

About

Mikhail V. Pugachev is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Mikhail V. Pugachev has authored 26 papers receiving a total of 347 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Organic Chemistry, 12 papers in Molecular Biology and 5 papers in Pharmacology. Recurrent topics in Mikhail V. Pugachev's work include Synthesis and Characterization of Heterocyclic Compounds (9 papers), Synthesis and biological activity (8 papers) and Antimicrobial agents and applications (5 papers). Mikhail V. Pugachev is often cited by papers focused on Synthesis and Characterization of Heterocyclic Compounds (9 papers), Synthesis and biological activity (8 papers) and Antimicrobial agents and applications (5 papers). Mikhail V. Pugachev collaborates with scholars based in Russia. Mikhail V. Pugachev's co-authors include Yurii G. Shtyrlin, Nikita V. Shtyrlin, Alfiya G. Iksanova, Elena Nikitina, Roman S. Pavelyev, Р. З. Мусин, Е. А. Бердников, О.А. Lodochnikova, Airat R. Kayumov and Konstantin V. Balakin and has published in prestigious journals such as SHILAP Revista de lepidopterología, Molecules and Tetrahedron Letters.

In The Last Decade

Mikhail V. Pugachev

24 papers receiving 344 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mikhail V. Pugachev Russia 12 269 134 31 26 25 26 347
Alfiya G. Iksanova Russia 12 280 1.0× 111 0.8× 29 0.9× 28 1.1× 20 0.8× 19 351
Nikita V. Shtyrlin Russia 16 415 1.5× 209 1.6× 51 1.6× 33 1.3× 40 1.6× 37 545
Swetha Kameswari Maddili China 9 214 0.8× 185 1.4× 22 0.7× 32 1.2× 20 0.8× 10 393
Zitai Sang China 13 228 0.8× 171 1.3× 13 0.4× 26 1.0× 46 1.8× 19 391
Taraknath Kundu India 9 183 0.7× 136 1.0× 25 0.8× 9 0.3× 13 0.5× 24 317
Danuta Drozdowska Poland 11 207 0.8× 155 1.2× 8 0.3× 33 1.3× 37 1.5× 30 393
Prashant Gahtori India 18 627 2.3× 146 1.1× 13 0.4× 34 1.3× 62 2.5× 39 795
Merve Nenni Türkiye 8 99 0.4× 69 0.5× 13 0.4× 25 1.0× 25 1.0× 19 324
Zhong‐Lin Zang China 11 272 1.0× 113 0.8× 20 0.6× 14 0.5× 15 0.6× 24 337
Prudencio Herradura United States 9 336 1.2× 78 0.6× 20 0.6× 40 1.5× 25 1.0× 10 410

Countries citing papers authored by Mikhail V. Pugachev

Since Specialization
Citations

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

Fields of papers citing papers by Mikhail V. Pugachev

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mikhail V. Pugachev. 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 Mikhail V. Pugachev. The network helps show where Mikhail V. Pugachev may publish in the future.

Co-authorship network of co-authors of Mikhail V. Pugachev

This figure shows the co-authorship network connecting the top 25 collaborators of Mikhail V. Pugachev. A scholar is included among the top collaborators of Mikhail V. Pugachev 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 Mikhail V. Pugachev. Mikhail V. Pugachev 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.
Pugachev, Mikhail V., et al.. (2025). Analgesic and anti-inflammatory properties of bipharmacophore prodrug derivatives based on pyridoxine and ketorolac. SHILAP Revista de lepidopterología. 167(3). 371–384.
2.
Shtyrlin, Nikita V., Elena Nikitina, Alfiya G. Iksanova, et al.. (2024). Quaternary Ammonium Compounds Based on Pyridoxine Derivatives: A New Class of Promising Antiseptics (A Review). Russian Journal of General Chemistry. 94(8). 1879–1904. 1 indexed citations
3.
Bondar, Oksana V., et al.. (2024). Anticancer Potential of Pyridoxine-Based Doxorubicin Derivatives: An In Vitro Study. Life. 14(3). 282–282. 2 indexed citations
4.
Shtyrlin, Nikita V., Airat R. Kayumov, Mikhail V. Pugachev, et al.. (2023). Synthesis and biological evaluation of fluoroquinolones containing a pyridoxine derivatives moiety. European Journal of Medicinal Chemistry. 261. 115798–115798. 2 indexed citations
5.
6.
Pugachev, Mikhail V., et al.. (2021). Synthesis and antitumor activity of novel pyridoxine-based structural analogs of saccharumoside-B. Medicinal Chemistry Research. 30(5). 1139–1150. 5 indexed citations
7.
Shtyrlin, Nikita V., et al.. (2021). DEVELOPMENT OF ANTIMICROBIAL AGENTS BASED ON PYRIDOXINE DERIVATIVES. 43–43.
8.
Shtyrlin, Nikita V., Mikhail V. Pugachev, Roman S. Pavelyev, et al.. (2020). Novel Bis-Ammonium Salts of Pyridoxine: Synthesis and Antimicrobial Properties. Molecules. 25(18). 4341–4341. 18 indexed citations
9.
Pugachev, Mikhail V., Roman S. Pavelyev, Alfiya G. Iksanova, et al.. (2020). Synthesis, antitumor activity and structure-activity studies of novel pyridoxine-based bioisosteric analogs of estradiol. Bioorganic & Medicinal Chemistry. 30. 115957–115957. 11 indexed citations
10.
Shtyrlin, Yurii G., Nikita V. Shtyrlin, Alfiya G. Iksanova, et al.. (2019). Chemistry of pyridoxine in drug design. Russian Chemical Bulletin. 68(5). 911–945. 37 indexed citations
11.
Pavelyev, Roman S., Oksana V. Bondar, Mikhail V. Pugachev, et al.. (2018). Synthesis and in vitro antitumor activity of novel alkenyl derivatives of pyridoxine, bioisosteric analogs of feruloyl methane. Bioorganic & Medicinal Chemistry. 26(22). 5824–5837. 14 indexed citations
12.
Pugachev, Mikhail V., et al.. (2018). Novel approach to 6-alkenyl-substituted pyridoxine derivatives based on the Heck reaction. Tetrahedron Letters. 59(33). 3220–3222. 1 indexed citations
13.
Pugachev, Mikhail V., Roman S. Pavelyev, Alfiya G. Iksanova, et al.. (2017). Synthesis and Antitumor Activity of Novel Pyridoxine-Based Bioisosteric Analogs of trans-Stilbenes. Journal of Chemistry. 2017. 1–7. 7 indexed citations
14.
Pugachev, Mikhail V., Roman S. Pavelyev, Oleg I. Gnezdilov, et al.. (2017). Wittig reactions of a bis-triphenylphosphonium pyridoxine derivative. Tetrahedron Letters. 58(8). 766–769. 7 indexed citations
15.
Pugachev, Mikhail V., et al.. (2016). Synthesis and antitumor activity of pyridoxine monoalkenyl derivatives. Russian Chemical Bulletin. 65(2). 532–536. 14 indexed citations
16.
Nikitina, Elena, Mikhail V. Pugachev, Nikita V. Shtyrlin, et al.. (2015). Antibacterial effects of quaternary bis-phosphonium and ammonium salts of pyridoxine on Staphylococcus aureus cells: A single base hitting two distinct targets?. World Journal of Microbiology and Biotechnology. 32(1). 5–5. 31 indexed citations
17.
Kayumov, Airat R., Elena Y. Trizna, Guzel R. Gazizova, et al.. (2015). New Derivatives of Pyridoxine Exhibit High Antibacterial Activity against Biofilm-EmbeddedStaphylococcusCells. BioMed Research International. 2015. 1–10. 38 indexed citations
18.
Pugachev, Mikhail V., Nikita V. Shtyrlin, Elena Nikitina, et al.. (2013). Synthesis and antibacterial activity of novel phosphonium salts on the basis of pyridoxine. Bioorganic & Medicinal Chemistry. 21(14). 4388–4395. 59 indexed citations
19.
Pugachev, Mikhail V., Nikita V. Shtyrlin, Alfiya G. Iksanova, et al.. (2013). Bis-phosphonium salts of pyridoxine: The relationship between structure and antibacterial activity. Bioorganic & Medicinal Chemistry. 21(23). 7330–7342. 38 indexed citations
20.
Shtyrlin, Nikita V., О.А. Lodochnikova, Mikhail V. Pugachev, et al.. (2010). Theoretical and experimental study on cyclic 6-methyl-2,3,4-tris(hydroxymethyl)pyridin-5-ol acetonides. Russian Journal of Organic Chemistry. 46(4). 561–567. 14 indexed citations

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