Oleg D. Mitkin
About
Oleg D. Mitkin is a scholar working on Organic Chemistry, Molecular Biology and Epidemiology.
According to data from OpenAlex, Oleg D. Mitkin has authored 63 papers receiving a total of 835 indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Organic Chemistry, 25 papers in Molecular Biology and 8 papers in Epidemiology. Recurrent topics in Oleg D. Mitkin's work include Synthesis and Biological Evaluation (21 papers), Synthesis and Reactivity of Heterocycles (13 papers) and Synthesis and Reactions of Organic Compounds (10 papers). Oleg D. Mitkin is often cited by papers focused on Synthesis and Biological Evaluation (21 papers), Synthesis and Reactivity of Heterocycles (13 papers) and Synthesis and Reactions of Organic Compounds (10 papers). Oleg D. Mitkin collaborates with scholars based in Russia, United States and Ukraine. Oleg D. Mitkin's co-authors include Alexandre V. Ivachtchenko, Ilya Okun, Sergey E. Tkachenko, M. Г. Кадиева, Volodymyr Kysil, Elena S. Golovina, Andrey A. Ivashchenko, Andrei G. Kutateladze, Sergey Tkachenko and Dmitry V. Kravchenko and has published in prestigious journals such as Journal of the American Chemical Society, SHILAP Revista de lepidopterología and Journal of Medicinal Chemistry.
In The Last Decade
Oleg D. Mitkin
58 papers receiving 721 citations
Peers
Oleg D. Mitkin
Casey C. McComas United States
Samuel W. Gerritz United States
Alan Stobie United Kingdom
Douglas C. Beshore United States
Fernando Rodrı́guez Spain
Maria Giovanna Pavani Italy
Frank Navas United States
Dieter Hamprecht United Kingdom
Jacobien K. von Frijtag Drabbe Künzel Netherlands
Stefan Peukert Switzerland
Citations per year, relative to Oleg D. Mitkin Oleg D. Mitkin (= 1×)
peers
Casey C. McComas
Countries citing papers authored by Oleg D. Mitkin
Since
Specialization
Citations
This map shows the geographic impact of Oleg D. Mitkin'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 Oleg D. Mitkin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Oleg D. Mitkin more than expected).
Fields of papers citing papers by Oleg D. Mitkin
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by Oleg D. Mitkin. 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 Oleg D. Mitkin. The network helps show where Oleg D. Mitkin may publish in the future.
Co-authorship network of co-authors of Oleg D. Mitkin
This figure shows the co-authorship network connecting the top 25 collaborators of Oleg D. Mitkin. A scholar is included among the top collaborators of Oleg D. Mitkin 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 Oleg D. Mitkin. Oleg D. Mitkin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Ivashchenko, Andrey A., Morozova Ma, Alina N. Egorova, et al.. (2021). Safety and efficacy of aviandr in patients with generalized anxiety disorder: A multicenter, randomized, double-blind, placebo-controlled, dose-finding, pilot study. Journal of Psychiatric Research. 143. 436–444.
2.
Ivashchenko, Andrey A., Yan A. Ivanenkov, Vladimir Aladinskiy, et al.. (2020). Synthesis, biological evaluation and in silico modeling of novel pan-genotypic NS5A inhibitors. Bioorganic & Medicinal Chemistry. 28(20). 115716–115716.
3.
Ivachtchenko, Alexandre V., Sergiy М. Kovalenko, Dmitry V. Kravchenko, et al.. (2019). Crystal structure, Hirshfeld analysis and a molecular docking study of a new inhibitor of the Hepatitis B virus (HBV): ethyl 5-methyl-1,1-dioxo-2-{[5-(pentan-3-yl)-1,2,4-oxadiazol-3-yl]methyl}-2H-1,2,6-thiadiazine-4-carboxylate. Acta Crystallographica Section E Crystallographic Communications. 76(1). 12–17.
4.
Ivachtchenko, Alexandre V., Yan A. Ivanenkov, Oleg D. Mitkin, et al.. (2015). Design, synthesis and biological evaluation of novel 5-oxo-2-thioxoimidazolidine derivatives as potent androgen receptor antagonists. European Journal of Medicinal Chemistry. 99. 51–66.
5.
Ivachtchenko, Alexandre V., Yan A. Ivanenkov, Oleg D. Mitkin, et al.. (2014). Novel oral anti-influenza drug candidate AV5080. Journal of Antimicrobial Chemotherapy. 69(7). 1892–1902.
6.
Mitkin, Oleg D., Irina A. Leneva, Елена А. Буланова, et al.. (2014). Synthesis and Antiviral Activity of Substituted 2,4-bis-aminomethyl-5-hydroxy-1H-indole-3-carboxylic Acid Ethyl Esters and their Derivatives. Pharmaceutical Chemistry Journal. 48(9). 569–581.
7.
Ivachtchenko, Alexandre V., et al.. (2014). Preclinical Development of ONC1-13B, Novel Antiandrogen for Prostate Cancer Treatment. Journal of Cancer. 5(2). 133–142.
8.
Ivachtchenko, Alexandre V., Yan A. Ivanenkov, Oleg D. Mitkin, et al.. (2014). Novel oral anti-influenza prodrug candidate AV5075S. Journal of Antimicrobial Chemotherapy. 69(5). 1311–1324.
9.
Ivachtchenko, Alexandre V., et al.. (2013). Synthesis of substituted diphenyl sulfones and their structure–activity relationship with the antagonism of 5-НТ6 receptors. Bioorganic & Medicinal Chemistry. 21(15). 4614–4627.
10.
Ivachtchenko, Alexandre V., Elena S. Golovina, M. Г. Кадиева, et al.. (2012). Serotonin 5-HT6 receptor antagonists. II. Synthesis and structure—activity relationship of 3-arylsulfonyl-2-methylthiopyrazolo[1,5-a]pyrimidines with substituents containing an amine in the 6-position. Pharmaceutical Chemistry Journal. 46(6). 337–345.
11.
Ivachtchenko, Alexandre V., Elena S. Golovina, M. Г. Кадиева, et al.. (2012). Antagonists of 5-HT6 receptors. Substituted 3-(phenylsulfonyl)pyrazolo[1,5-a]pyrido[3,4-e]pyrimidines and 3-(phenylsulfonyl)pyrazolo[1,5-a]pyrido[4,3-d]pyrimidines—Synthesis and ‘structure–activity’ relationship. Bioorganic & Medicinal Chemistry Letters. 22(13). 4273–4280.
12.
Ivachtchenko, Alexandre V., Elena S. Golovina, M. Г. Кадиева, et al.. (2011). Synthesis and SAR of 3-arylsulfonyl-pyrazolo[1,5-a]pyrimidines as potent serotonin 5-HT6 receptor antagonists. Bioorganic & Medicinal Chemistry. 19(4). 1482–1491.
13.
Ivachtchenko, Alexandre V., Elena S. Golovina, M. Г. Кадиева, et al.. (2010). (3-Phenylsulfonylcycloalkano[eandd]pyrazolo[1,5-a]pyrimidin-2-yl)amines: Potent and Selective Antagonists of the Serotonin 5-HT6Receptor. Journal of Medicinal Chemistry. 53(14). 5186–5196.
14.
Okun, Ilya, et al.. (2010). From Anti-allergic to Anti-Alzheimer ’ s: Molecular Pharmacology of Dimebon™. Current Alzheimer Research. 7(2). 97–112.
15.
Ivachtchenko, Alexandre V., Oleg D. Mitkin, Sergey E. Tkachenko, Ilya Okun, & Volodymyr Kysil. (2009). 8-Sulfonyl-substituted tetrahydro-1 H -pyrido[4,3- b ]indoles as 5-HT 6 receptor antagonists. European Journal of Medicinal Chemistry. 45(2). 782–789.
16.
Ivachtchenko, Alexandre V., et al.. (2009). Synthesis and Biological Evaluation of Novel 5,8‐Disubstituted‐2‐methyl‐2,3,4,5‐tetrahydro‐1H‐pyrido[4,3‐b] indoles as 5‐HT6and H1Receptors Antagonists. Archiv der Pharmazie. 342(12). 740–747.
17.
Ivachtchenko, Alexandre V., et al.. (2009). Synthesis and biological activity of 5-styryl and 5-phenethyl-substituted 2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indoles. Bioorganic & Medicinal Chemistry Letters. 20(1). 78–82.
18.
Ivachtchenko, Alexandre V., Oleg D. Mitkin, Volodymyr Kysil, et al.. (2009). Synthesis and biological evaluation of novel γ-carboline analogues of Dimebon as potent 5-HT6 receptor antagonists. Bioorganic & Medicinal Chemistry Letters. 19(12). 3183–3187.
19.
Mitkin, Oleg D. & M. A. Yurovskaya. (2000). Quaternization of electron-deficient pyridines containing two electron-withdrawing substituents. Chemistry of Heterocyclic Compounds. 36(1). 47–48.
20.
Yurovskaya, M. A., Oleg D. Mitkin, & В. Н. Нестеров. (1996). Autohetarylation of 4,6-dimethyl-5-nitro-2chloro-3-cyanopyridine ? An unexpected transformation in the presence of bases. Chemistry of Heterocyclic Compounds. 32(5). 585–589.
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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