Н. И. Комарова

922 total citations
60 papers, 736 citations indexed

About

Н. И. Комарова is a scholar working on Molecular Biology, Organic Chemistry and Pharmacology. According to data from OpenAlex, Н. И. Комарова has authored 60 papers receiving a total of 736 indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Molecular Biology, 21 papers in Organic Chemistry and 9 papers in Pharmacology. Recurrent topics in Н. И. Комарова's work include Natural product bioactivities and synthesis (10 papers), DNA and Nucleic Acid Chemistry (8 papers) and Pharmacological Effects of Natural Compounds (6 papers). Н. И. Комарова is often cited by papers focused on Natural product bioactivities and synthesis (10 papers), DNA and Nucleic Acid Chemistry (8 papers) and Pharmacological Effects of Natural Compounds (6 papers). Н. И. Комарова collaborates with scholars based in Russia, United Kingdom and Italy. Н. И. Комарова's co-authors include Нариман Ф. Салахутдинов, Д. В. Корчагина, Константин П. Волчо, М. П. Половинка, Olga A. Luzina, Т. М. Хоменко, Jóhannes Reynisson, Oksana V. Salomatina, Olga I. Lavrik and Alexandra L. Zakharenko and has published in prestigious journals such as Nucleic Acids Research, FEBS Letters and International Journal of Molecular Sciences.

In The Last Decade

Н. И. Комарова

57 papers receiving 717 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Н. И. Комарова Russia	15	328	245	102	96	93	60	736
Kakali Bhadra India	14	442 1.3×	202 0.8×	208 2.0×	73 0.8×	45 0.5×	33	856
Praveen Kumar India	15	241 0.7×	547 2.2×	74 0.7×	156 1.6×	35 0.4×	50	837
Chen Qing China	20	432 1.3×	303 1.2×	217 2.1×	212 2.2×	77 0.8×	55	962
Zhiqin Ji China	18	475 1.4×	306 1.2×	194 1.9×	203 2.1×	62 0.7×	62	882
Huizhe Lu China	16	485 1.5×	241 1.0×	125 1.2×	145 1.5×	41 0.4×	61	946
Ragini G. Bodade India	13	264 0.8×	530 2.2×	141 1.4×	78 0.8×	51 0.5×	26	875
Wenyan Xu China	16	484 1.5×	134 0.5×	39 0.4×	196 2.0×	34 0.4×	36	813
Michael Dreyer Germany	19	315 1.0×	488 2.0×	99 1.0×	184 1.9×	50 0.5×	31	979
Guiyang Yao China	19	479 1.5×	355 1.4×	128 1.3×	54 0.6×	19 0.2×	42	860
Nelilma Correia Romeiro Brazil	18	385 1.2×	662 2.7×	185 1.8×	66 0.7×	21 0.2×	62	1.2k

Countries citing papers authored by Н. И. Комарова

Since Specialization

Citations

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

Fields of papers citing papers by Н. И. Комарова

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Н. И. Комарова

This figure shows the co-authorship network connecting the top 25 collaborators of Н. И. Комарова. A scholar is included among the top collaborators of Н. И. Комарова 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 Н. И. Комарова. Н. И. Комарова is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Salomatina, Oksana V., Alexandra L. Zakharenko, Н. И. Комарова, et al.. (2024). New Dual Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 and 2 Based on Deoxycholic Acid: Design, Synthesis, Cytotoxicity, and Molecular Modeling. Molecules. 29(3). 581–581. 1 indexed citations

Штро, Анна А., Sophia S. Borisevich, Т. М. Хоменко, et al.. (2024). Design, synthesis and antiviral evaluation of triazole-linked 7-hydroxycoumarin–monoterpene conjugates as inhibitors of RSV replication. RSC Medicinal Chemistry. 16(3). 1151–1171.

Комарова, Н. И., et al.. (2023). SYNTHESIS OF GLYCIVIR DERIVATIVES USING MODIFICATION OF SYNTHESIS PROCEDURE STUDYING THEIR ANTIVIRAL ACTIVITY AGAINST ENV-PSEUDOVIROUSES HIV-1. chemistry of plant raw material. 387–395.

Salomatina, Oksana V., Aleksandra V. Sen’kova, Innokenty A. Savin, et al.. (2022). Novel Epoxides of Soloxolone Methyl: An Effect of the Formation of Oxirane Ring and Stereoisomerism on Cytotoxic Profile, Anti-Metastatic and Anti-Inflammatory Activities In Vitro and In Vivo. International Journal of Molecular Sciences. 23(11). 6214–6214. 10 indexed citations

Salomatina, Oksana V., Alexandra L. Zakharenko, Olga D. Zakharova, et al.. (2020). Deoxycholic acid as a molecular scaffold for tyrosyl-DNA phosphodiesterase 1 inhibition: A synthesis, structure–activity relationship and molecular modeling study. Steroids. 165. 108771–108771. 25 indexed citations

Kuzmich, Alexandra S., Т. М. Хоменко, Sergey N. Fedorov, et al.. (2016). Cytotoxic and cancer preventive activity of benzotrithioles and benzotrithiole oxides, synthetic analogues of varacins. Medicinal Chemistry Research. 26(2). 397–404. 4 indexed citations

Boyarskikh, U. A., Михаил В. Хвостов, Dmitry S. Baev, et al.. (2015). Hypolipidemic Berberine Derivatives with a Reduced Aromatic Ring C. Chemistry of Natural Compounds. 51(5). 916–922. 13 indexed citations

Naumenko, Sergey, et al.. (2014). Cardioprotective Effect of Resveratrol and Resveratroloside. Cardiovascular & Hematological Agents in Medicinal Chemistry. 11(3). 207–210. 8 indexed citations

Суслов, Е. В., Д. В. Корчагина, Н. И. Комарова, et al.. (2012). Synthesis and anxiolytic activity of 2-aminoadamantane derivatives containing monoterpene fragments. Pharmaceutical Chemistry Journal. 46(5). 263–265. 24 indexed citations

10.

Rogachev, Artem D., et al.. (2012). Reaction of several resveratrol glycoside derivatives with hypochlorites in various media. Chemistry of Natural Compounds. 48(1). 1–7. 6 indexed citations

11.

Boyarskikh, U. A., Н. И. Комарова, М. П. Половинка, et al.. (2011). LDLR up-regulatory activity of berberine and its bromo and iodo derivatives in human liver HepG2 cells. Doklady Chemistry. 439(1). 204–208. 9 indexed citations

12.

Хоменко, Т. М., Константин П. Волчо, Н. И. Комарова, & Нариман Ф. Салахутдинов. (2008). An efficient procedure for the synthesis of Esomeprazole using a titanium complex with two chiral ligands. Russian Journal of Organic Chemistry. 44(1). 124–127. 12 indexed citations

13.

Половинка, М. П., et al.. (2008). Low-molecular-weight phenolic compounds from Hedysarum theinum roots. Chemistry of Natural Compounds. 44(1). 31–34. 31 indexed citations

14.

Волчо, Константин П., et al.. (2008). New chiral Schiff bases derived from (+)- and (−)-α-pinenes in the metal complex catalyzed asymmetric oxidation of sulfides. Russian Chemical Bulletin. 57(1). 108–117. 21 indexed citations

15.

Половинка, М. П., et al.. (2008). Fatty-acid composition and secondary metabolites from slightly polar extracts of the aerial part of Primula macrocalyx. Chemistry of Natural Compounds. 44(5). 564–568. 14 indexed citations

16.

Rogachev, Artem D., et al.. (2007). Phytochemical Studies of Rhododendron adamsii Rehder. Quantitative Determination of Ursolic and Oleanolic Acids in Some Representatives of Ericaceae Family. 2 indexed citations

17.

Репкова, М. Н., et al.. (2002). Oligoribonucleotides containing an aminoalkyl group at the N(4) atom of cytosine as precursors of new reagents for site-specific modifications of biopolymers. Russian Chemical Bulletin. 51(7). 1194–1197. 2 indexed citations

18.

Denisov, A. Yu., et al.. (2001). Long-lived reactive intermediate photogenerated from N-(5-azido-2-nitrobenzoyl)-N′-(d-biotinyl)-1,2-diaminoethane as an affinity reagent to streptavidin. Journal of Photochemistry and Photobiology B Biology. 61(1-2). 68–77. 1 indexed citations

19.

Bonora, Gian Maria, et al.. (1999). Biological Properties of Antisense Oligonucleotides Conjugated to Different High-Molecular Mass Poly(Ethylen Glycols). Nucleosides and Nucleotides. 18(6-7). 1723–1725. 3 indexed citations

20.

Grachev, M.A., et al.. (1971). On the heterogenity of individual tRNA^val₁ that arises in the course of modification with CME‐carbodiimide. FEBS Letters. 17(2). 269–272. 3 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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