Л. А. Балтина

2.7k total citations
137 papers, 1.8k citations indexed

About

Л. А. Балтина is a scholar working on Molecular Biology, Pharmacology and Immunology. According to data from OpenAlex, Л. А. Балтина has authored 137 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 97 papers in Molecular Biology, 93 papers in Pharmacology and 28 papers in Immunology. Recurrent topics in Л. А. Балтина's work include Pharmacological Effects of Natural Compounds (91 papers), Natural product bioactivities and synthesis (87 papers) and Toxin Mechanisms and Immunotoxins (28 papers). Л. А. Балтина is often cited by papers focused on Pharmacological Effects of Natural Compounds (91 papers), Natural product bioactivities and synthesis (87 papers) and Toxin Mechanisms and Immunotoxins (28 papers). Л. А. Балтина collaborates with scholars based in Russia, Taiwan and Belarus. Л. А. Балтина's co-authors include Р. М. Кондратенко, Г. А. Толстиков, Lia A. Baltina, Г. А. Толстиков, О. Б. Флехтер, Jindřich Činátl, Ф. З. Галин, Martin Michaelis, Hans Wilhelm Doerr and E. I. Boreko and has published in prestigious journals such as International Journal of Molecular Sciences, Journal of Medicinal Chemistry and Current Medicinal Chemistry.

In The Last Decade

Л. А. Балтина

129 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Л. А. Балтина Russia 20 1.0k 1.0k 368 352 209 137 1.8k
Hai‐Lin Qin China 21 652 0.6× 359 0.3× 261 0.7× 90 0.3× 240 1.1× 96 1.5k
Catherine Neto United States 24 775 0.7× 337 0.3× 582 1.6× 64 0.2× 155 0.7× 48 2.2k
Guo‐Cai Wang China 28 1.5k 1.4× 497 0.5× 704 1.9× 101 0.3× 262 1.3× 145 2.5k
J.M. Pezzuto United States 25 1.4k 1.3× 470 0.5× 700 1.9× 97 0.3× 209 1.0× 38 2.6k
L. Mark Cosentino United States 23 1.8k 1.7× 335 0.3× 563 1.5× 142 0.4× 165 0.8× 30 3.0k
Adnan J. Al‐Rehaily Saudi Arabia 26 710 0.7× 436 0.4× 961 2.6× 61 0.2× 238 1.1× 142 2.1k
Fatma Ergün Türkiye 20 528 0.5× 238 0.2× 747 2.0× 206 0.6× 208 1.0× 63 1.7k
Banasri Hazra India 28 741 0.7× 254 0.2× 512 1.4× 86 0.2× 342 1.6× 77 2.0k
Yun‐Bao Ma China 34 2.1k 2.0× 831 0.8× 1.1k 2.9× 124 0.4× 380 1.8× 174 3.7k
Hirotsugu Miyashiro Japan 21 782 0.8× 391 0.4× 496 1.3× 102 0.3× 221 1.1× 31 1.7k

Countries citing papers authored by Л. А. Балтина

Since Specialization
Citations

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

Fields of papers citing papers by Л. А. Балтина

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Л. А. Балтина

This figure shows the co-authorship network connecting the top 25 collaborators of Л. А. Балтина. A scholar is included among the top collaborators of Л. А. Балтина 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 Л. А. Балтина. Л. А. Балтина 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.
Lu, Chih‐Hao, Yeh Chen, Wen‐Chi Su, et al.. (2024). Glycyrrhizic acid conjugates with amino acid methyl esters target the main protease, exhibiting antiviral activity against wild-type and nirmatrelvir-resistant SARS-CoV-2 variants. Antiviral Research. 227. 105920–105920. 1 indexed citations
3.
Балтина, Л. А., et al.. (2024). Synthesis and Antiulcer Activity of Aromatic and Heterocyclic Amides of 3-O-Acetylglycyrrhetic Acid. Pharmaceutical Chemistry Journal. 57(11). 1717–1725. 1 indexed citations
4.
Балтина, Л. А., et al.. (2024). Pharmacological Properties of Acetylsalicylic Acid and its Complex with Glycyrrhizic Acid as a Promising Dosage form (Review). Pharmaceutical Chemistry Journal. 58(1). 27–34. 1 indexed citations
5.
Балтина, Л. А., et al.. (2023). Cytotoxic Activity of A-Modified Licorice Triterpenoid Derivatives. Pharmaceutical Chemistry Journal. 57(5). 637–641. 1 indexed citations
6.
Hour, Mann‐Jen, Yeh Chen, Л. А. Балтина, et al.. (2022). Glycyrrhizic Acid Derivatives Bearing Amino Acid Residues in the Carbohydrate Part as Dengue Virus E Protein Inhibitors: Synthesis and Antiviral Activity. International Journal of Molecular Sciences. 23(18). 10309–10309. 10 indexed citations
7.
Балтина, Л. А., Hsueh‐Chou Lai, Su-Hua Huang, et al.. (2021). Glycyrrhetinic acid derivatives as Zika virus inhibitors: Synthesis and antiviral activity in vitro. Bioorganic & Medicinal Chemistry. 41. 116204–116204. 34 indexed citations
8.
Балтина, Л. А., et al.. (2019). Paeoniflorin benzoates: synthesis and influence on learning and memory of aged rats in the passive avoidance task. Natural Product Research. 35(16). 2668–2676. 4 indexed citations
9.
Балтина, Л. А., Su‐Hua Huang, Hsueh‐Chou Lai, et al.. (2019). Glycyrrhizic acid derivatives as Dengue virus inhibitors. Bioorganic & Medicinal Chemistry Letters. 29(20). 126645–126645. 43 indexed citations
10.
Балтина, Л. А., Л. А. Балтина, Р. М. Кондратенко, et al.. (2009). A simple method of synthesis of triterpene glycosides similar to glycyrrhizic acid and their hepatoprotective activity in vitro. Russian Journal of Bioorganic Chemistry. 35(5). 686–95. 3 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.
Балтина, Л. А., et al.. (2006). Synthesis of glycyrrhizic acid conjugates containing L-lysine. Chemistry of Natural Compounds. 42(5). 543–548. 9 indexed citations
13.
Флехтер, О. Б., et al.. (2003). Oxidation of Betulin and Its Monoacetates by “Activated” DMSO. Chemistry of Natural Compounds. 39(2). 207–211. 4 indexed citations
14.
Кондратенко, Р. М., et al.. (2003). Transformations of Glycyrrhizic Acid: XV. Synthesis of Triterpene Saponins with Monosaccharide Residues Attached through Ester Bonds. Russian Journal of Bioorganic Chemistry. 29(6). 601–605. 2 indexed citations
15.
Балтина, Л. А., О. Б. Флехтер, E. I. Boreko, et al.. (2003). Lupane triterpenes and derivatives with antiviral activity. Bioorganic & Medicinal Chemistry Letters. 13(20). 3549–3552. 99 indexed citations
16.
Флехтер, О. Б., et al.. (2002). Synthesis of Ketals of Methyl 3-Oxo-lup-20(29)-en-28-oate. Chemistry of Natural Compounds. 38(6). 583–585. 2 indexed citations
17.
Балтина, Л. А., et al.. (1997). Simplified stereoselective synthesis of triterpene 3-O-2-deoxy-α-D-glycosides. Mendeleev Communications. 7(1). 3–4. 3 indexed citations
18.
Балтина, Л. А., et al.. (1994). Preparation of glycyrrhizic acid from licorice extracts. Pharmaceutical Chemistry Journal. 28(9). 674–678. 2 indexed citations
19.
Балтина, Л. А., et al.. (1990). Synthesis of glycopeptide derivatives of glycyrrhizinic acid and their immunomodulatory properties. Pharmaceutical Chemistry Journal. 24(2). 110–114. 1 indexed citations
20.
Толстиков, Г. А., et al.. (1989). [Transformation of glycyrrhizic acid. Synthesis of glycopeptides of glycyrrhizic acid monomethyl ether, having anti-inflammatory and immunostimulating action].. PubMed. 15(3). 392–8. 1 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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