А. Г. Покровский

474 total citations
46 papers, 393 citations indexed

About

А. Г. Покровский is a scholar working on Molecular Biology, Organic Chemistry and Pharmacology. According to data from OpenAlex, А. Г. Покровский has authored 46 papers receiving a total of 393 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 15 papers in Organic Chemistry and 7 papers in Pharmacology. Recurrent topics in А. Г. Покровский's work include Natural product bioactivities and synthesis (13 papers), Synthesis and biological activity (8 papers) and Pharmacological Effects of Natural Compounds (7 papers). А. Г. Покровский is often cited by papers focused on Natural product bioactivities and synthesis (13 papers), Synthesis and biological activity (8 papers) and Pharmacological Effects of Natural Compounds (7 papers). А. Г. Покровский collaborates with scholars based in Russia, Mongolia and Italy. А. Г. Покровский's co-authors include Л. А. Балтина, Elvira E. Shults, Р. М. Кондратенко, Г. А. Толстиков, Г. А. Толстиков, М. М. Шакиров, Tatyana V. Rybalova, Л. Д. Раднаева, Dmitry S. Baev and Нариман Ф. Салахутдинов and has published in prestigious journals such as Molecules, Journal of Ethnopharmacology and Steroids.

In The Last Decade

А. Г. Покровский

43 papers receiving 381 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
А. Г. Покровский Russia 11 196 123 103 73 41 46 393
Shou-Fang Wu Taiwan 10 216 1.1× 136 1.1× 68 0.7× 67 0.9× 17 0.4× 10 493
Gao-Xiong Rao China 15 225 1.1× 190 1.5× 81 0.8× 112 1.5× 26 0.6× 48 586
Di‐An Sun China 15 301 1.5× 84 0.7× 96 0.9× 81 1.1× 24 0.6× 34 481
P. Vijayan India 11 168 0.9× 114 0.9× 79 0.8× 172 2.4× 28 0.7× 21 547
Mark Tristan J. Quimque Philippines 13 162 0.8× 64 0.5× 74 0.7× 52 0.7× 20 0.5× 26 447
Hanne L. Ziegler Denmark 11 375 1.9× 91 0.7× 63 0.6× 108 1.5× 34 0.8× 12 513
Xun Luo China 6 167 0.9× 90 0.7× 101 1.0× 41 0.6× 16 0.4× 8 494
Kanwal Raj India 15 156 0.8× 112 0.9× 78 0.8× 102 1.4× 12 0.3× 32 393
Ahmed M. Zaghloul Egypt 13 230 1.2× 89 0.7× 56 0.5× 152 2.1× 14 0.3× 29 471
Macki Kaloga Germany 12 289 1.5× 105 0.9× 80 0.8× 187 2.6× 24 0.6× 18 536

Countries citing papers authored by А. Г. Покровский

Since Specialization
Citations

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

Fields of papers citing papers by А. Г. Покровский

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of А. Г. Покровский

This figure shows the co-authorship network connecting the top 25 collaborators of А. Г. Покровский. A scholar is included among the top collaborators of А. Г. Покровский 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 А. Г. Покровский. А. Г. Покровский 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.
2.
Shults, Elvira E., et al.. (2020). Chromones and coumarins from Saposhnikovia divaricata (Turcz.) Schischk. Growing in Buryatia and Mongolia and their cytotoxicity. Journal of Ethnopharmacology. 261. 112517–112517. 36 indexed citations
3.
4.
Baev, Dmitry S., et al.. (2019). Design, synthesis, cytotoxicity, and molecular modeling study of 2,4,6-trisubstituted pyrimidines with anthranilate ester moiety. Medicinal Chemistry Research. 28(4). 545–558. 22 indexed citations
5.
Покровский, А. Г., et al.. (2017). Comparative Study of Fusogenic Activity of H1 and H5 Subtypes Influenza Virus Hemagglutinins. Bulletin of Experimental Biology and Medicine. 164(1). 85–89. 1 indexed citations
6.
Luzina, Olga A., et al.. (2016). Synthesis and cytotoxic activity of usnic acid cyanoethyl derivatives. Russian Chemical Bulletin. 65(2). 566–569. 3 indexed citations
7.
Шакиров, М. М., et al.. (2014). Synthesis and Cytotoxic Activity of Lupane Triterpenoids Containing 1,3,4-Oxadiazoles. Chemistry of Natural Compounds. 10 indexed citations
8.
Shults, Elvira E., et al.. (2013). Synthetic transformation of higher terpenoids 31. Synthesis of 1,2,3-triazolyl-containing furan labdanoids and studies of their cytotoxic activity. Russian Chemical Bulletin. 62(9). 2046–2055. 9 indexed citations
9.
Shults, Elvira E., et al.. (2013). Furocoumarins from Peucedanum baicalense of mongolia flora and their cytotoxic activity. Chemistry of Natural Compounds. 49(1). 99–102. 3 indexed citations
10.
Балтина, Л. А., et al.. (2010). Synthesis and antiviral activity of 18α-glycyrrhizic acid and its esters. Pharmaceutical Chemistry Journal. 44(6). 299–302. 17 indexed citations
11.
Балтина, Л. А., et al.. (2009). Prospects for the creation of new antiviral drugs based on glycyrrhizic acid and its derivatives (a review). Pharmaceutical Chemistry Journal. 43(10). 539–548. 63 indexed citations
12.
Покровский, А. Г., et al.. (2006). Activation of apoptosis by derivatives of betulinic acid in human tumor cells in vitro. Doklady Biochemistry and Biophysics. 407(1). 94–97. 5 indexed citations
13.
Jasko, Maxim V., et al.. (2006). New derivatives of alkyl-and aminocarbonylphosphonic acids containing 3′-azido-3′-deoxythymidine. Russian Journal of Bioorganic Chemistry. 32(6). 542–546. 8 indexed citations
14.
Покровский, А. Г., et al.. (2004). Fluorinated Derivatives of Benz[4,5]imidazo[1,2-b][1,3] thiazole—Inhibitors of Reproduction of Measles Virus. Doklady Biochemistry and Biophysics. 398(1-6). 285–287. 4 indexed citations
15.
Кондратенко, Р. М., Л. А. Балтина, Е. В. Васильева, et al.. (2004). The Synthesis and Antiviral Activity of Glycyrrhizic Acid Conjugates with α-D-Glucosamine and Some Glycosylamines. Russian Journal of Bioorganic Chemistry. 30(3). 275–282. 8 indexed citations
16.
Shirokova, Elena A., Maxim V. Jasko, Anastasia L. Khandazhinskaya, et al.. (2004). New Phosphonoformic Acid Derivatives of 3′-Azido-3′-Deoxythymidine. Russian Journal of Bioorganic Chemistry. 30(3). 242–249. 3 indexed citations
17.
Семенова, Е. А., et al.. (2003). Inhibition of the Activity of Recombinant HIV-1 Integrase by Derivatives of Higher Terpenoids. Doklady Biochemistry and Biophysics. 391(1-6). 218–220. 2 indexed citations
18.
Ilina, Tatiana V., Е. А. Семенова, А. Г. Покровский, et al.. (2002). Inhibition of HIV-1 Reverse Transcriptase by Aryl-Substituted Naphto- and Anthraquinones. Doklady Biochemistry and Biophysics. 382(1-6). 56–59. 17 indexed citations
19.
Флехтер, О. Б., Л. А. Балтина, Ф. С. Зарудий, et al.. (2002). Synthesis and Pharmacological Activity of Betulin Dinicotinate. Russian Journal of Bioorganic Chemistry. 28(6). 494–500. 22 indexed citations
20.
Mamaeva, Olga, et al.. (2001). Nonintegrated Circular Forms of the HIV-1 Provirus DNA in Experimental HIV Infection. Doklady Biochemistry and Biophysics. 377(1-6). 116–118. 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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