Р. М. Кондратенко

981 total citations
51 papers, 797 citations indexed

About

Р. М. Кондратенко is a scholar working on Pharmacology, Molecular Biology and Immunology. According to data from OpenAlex, Р. М. Кондратенко has authored 51 papers receiving a total of 797 indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Pharmacology, 32 papers in Molecular Biology and 12 papers in Immunology. Recurrent topics in Р. М. Кондратенко's work include Pharmacological Effects of Natural Compounds (43 papers), Natural product bioactivities and synthesis (27 papers) and Toxin Mechanisms and Immunotoxins (12 papers). Р. М. Кондратенко is often cited by papers focused on Pharmacological Effects of Natural Compounds (43 papers), Natural product bioactivities and synthesis (27 papers) and Toxin Mechanisms and Immunotoxins (12 papers). Р. М. Кондратенко collaborates with scholars based in Russia, Austria and Taiwan. Р. М. Кондратенко's co-authors include Л. А. Балтина, Г. А. Толстиков, Lia A. Baltina, Martin Michaelis, Jindřich Činátl, Hans Wilhelm Doerr, Г. А. Толстиков, А. Г. Покровский, Jung‐Chung Lin and Jaw‐Ming Cherng and has published in prestigious journals such as Journal of Medicinal Chemistry, Virus Research and Antiviral Research.

In The Last Decade

Р. М. Кондратенко

49 papers receiving 774 citations

Peers

Countries citing papers authored by Р. М. Кондратенко

Since Specialization

Citations

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

Fields of papers citing papers by Р. М. Кондратенко

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Р. М. Кондратенко. 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 Р. М. Кондратенко. The network helps show where Р. М. Кондратенко may publish in the future.

Co-authorship network of co-authors of Р. М. Кондратенко

This figure shows the co-authorship network connecting the top 25 collaborators of Р. М. Кондратенко. A scholar is included among the top collaborators of Р. М. Кондратенко 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 Р. М. Кондратенко. Р. М. Кондратенко 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

#	Work	Indexed citations
1	Cytotoxic Activity of A-Modified Licorice Triterpenoid Derivatives 2023 ·Pharmaceutical Chemistry Journal ·Л. А. Балтина, (unknown), (unknown), (unknown), Р. М. Кондратенко	1
2	Синтез конъюгатов глицирризиновой кислоты с s-бензил-L-цистеином и их противовирусная активность 2021 ·Химико-фармацевтический журнал ·Л. А. Балтина, Р. М. Кондратенко, (unknown), (unknown)	1
3	1-(3-Dimethylaminopropyl)-3-Ethylcarbodiimide in the Synthesis of Glycyrrhizic Acid Amino-Acid Conjugates 2020 ·Chemistry of Natural Compounds ·Л. А. Балтина, Р. М. Кондратенко, (unknown)	6
4	Antiviral activity of glycyrrhizic acid conjugates with amino acid esters against Zika virus 2020 ·Virus Research ·Л. А. Балтина, Mann‐Jen Hour, (unknown), (unknown), Su-Hua Huang, Hsueh‐Chou Lai, Р. М. Кондратенко, (unknown), Marat S. Yunusov, Cheng‐Wen Lin	19
5	Paeoniflorin benzoates: synthesis and influence on learning and memory of aged rats in the passive avoidance task 2019 ·Natural Product Research ·Л. А. Балтина, (unknown), (unknown), (unknown), (unknown), Lia A. Baltina, Р. М. Кондратенко	4
6	Synthesis and Anti-HIV-1 Activity of Olean-9(11),12(13)-Dien-30-Oic Acid 3β-(2-O-β-D-Glucuronopyranosyl-β-D-Glucuronopyranoside) 2014 ·Pharmaceutical Chemistry Journal ·Л. А. Балтина, (unknown), Р. М. Кондратенко, (unknown), (unknown), Tatiana V. Ilina	5
7	Synthesis and anti-HIV-1 activity of new conjugates of 18β- and 18α-glycyrrhizic acids with aspartic acid esters 2012 ·Chemistry of Natural Compounds ·Л. А. Балтина, (unknown), Р. М. Кондратенко, (unknown)	16
8	Synthesis and anti-HIV activity of triterpene 3-O-galactopyranosides, analogs of glycyrrhizic acid 2010 ·Chemistry of Natural Compounds ·Л. А. Балтина, Р. М. Кондратенко, (unknown), Sergey A. Nepogodiev, Robert A. Field	4
9	Synthesis and antiviral activity of 18α-glycyrrhizic acid and its esters 2010 ·Pharmaceutical Chemistry Journal ·Л. А. Балтина, (unknown), Р. М. Кондратенко, (unknown), А. Г. Покровский	17
10	A simple method of synthesis of triterpene glycosides similar to glycyrrhizic acid and their hepatoprotective activity in vitro 2009 ·Russian Journal of Bioorganic Chemistry ·(unknown), Л. А. Балтина, Р. М. Кондратенко, Sergey A. Nepogodiev, Robert A. Field, Olaf Kunert, Mei-chin Yin	3
11	Prospects for the creation of new antiviral drugs based on glycyrrhizic acid and its derivatives (a review) 2009 ·Pharmaceutical Chemistry Journal ·Л. А. Балтина, Р. М. Кондратенко, (unknown), А. Г. Покровский, Г. А. Толстиков	63
12	Synthesis and immunomodulating activity of new glycopeptides of glycyrrhizic acid containing residues of L-glutamic acid 2006 ·Russian Journal of Bioorganic Chemistry ·Р. М. Кондратенко, Л. А. Балтина, (unknown), Г. А. Толстиков	10
13	Synthesis and high-resolution NMR spectra of A-nor-derivatives of 11-deoxyglycyrrhetic acid 2006 ·Chemistry of Natural Compounds ·(unknown), Л. А. Балтина, Р. М. Кондратенко, Olaf Kunert, Л. В. Спирихин, Ф. З. Галин, Г. А. Толстиков	10
14	Synthesis and Immunostimulating Activity of Cysteine-Containing Derivatives of Glycyrrhizic Acid 2004 ·Russian Journal of Bioorganic Chemistry ·Р. М. Кондратенко, Л. А. Балтина, Е. В. Васильева, (unknown), (unknown), (unknown), (unknown), (unknown), Г. А. Толстиков	8
15	Transformations of Glycyrrhizic Acid: XV. Synthesis of Triterpene Saponins with Monosaccharide Residues Attached through Ester Bonds 2003 ·Russian Journal of Bioorganic Chemistry ·Р. М. Кондратенко, Л. А. Балтина, (unknown), Е. В. Васильева, (unknown), (unknown), Г. А. Толстиков	2
16	Complexes of Glycyrrhizinic Acid with Antimicrobial Substances. 2003 ·ChemInform ·Р. М. Кондратенко, Л. А. Балтина, (unknown), (unknown), Ф. С. Зарудий, (unknown), (unknown), (unknown), Г. А. Толстиков	2
17	Crystalline Glycyrrhizic Acid Synthesized from Commercial Glycyrram. Immunomodulant Properties of High-Purity Glycyrrhizic Acid 2001 ·Pharmaceutical Chemistry Journal ·Р. М. Кондратенко, Л. А. Балтина, (unknown), (unknown), (unknown), Г. А. Толстиков	19
18	Synthesis of Glycyrrhizic Acid from Glycyrram and Pharmaciological Characterization of the Product 2001 ·Pharmaceutical Chemistry Journal ·Л. А. Балтина, Р. М. Кондратенко, (unknown), О. Б. Флехтер, Yu. I. Murinov, (unknown), Ф. С. Зарудий, (unknown), Г. А. Толстиков	5
19	Preparation of glycyrrhizic acid from licorice extracts 1994 ·Pharmaceutical Chemistry Journal ·Л. А. Балтина, (unknown), (unknown), Р. М. Кондратенко, Г. А. Толстиков	2
20	[Transformation of glycyrrhizic acid. Synthesis of glycopeptides of glycyrrhizic acid monomethyl ether, having anti-inflammatory and immunostimulating action]. 1989 ·PubMed ·Г. А. Толстиков, Л. А. Балтина, Р. М. Кондратенко, (unknown), (unknown)	1

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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