Dmytro S. Radchenko

2.9k total citations · 2 hit papers
55 papers, 1.8k citations indexed

About

Dmytro S. Radchenko is a scholar working on Molecular Biology, Organic Chemistry and Pharmaceutical Science. According to data from OpenAlex, Dmytro S. Radchenko has authored 55 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 32 papers in Organic Chemistry and 16 papers in Pharmaceutical Science. Recurrent topics in Dmytro S. Radchenko's work include Chemical Synthesis and Analysis (28 papers), Fluorine in Organic Chemistry (16 papers) and Computational Drug Discovery Methods (11 papers). Dmytro S. Radchenko is often cited by papers focused on Chemical Synthesis and Analysis (28 papers), Fluorine in Organic Chemistry (16 papers) and Computational Drug Discovery Methods (11 papers). Dmytro S. Radchenko collaborates with scholars based in Ukraine, Germany and United States. Dmytro S. Radchenko's co-authors include Oleksandr O. Grygorenko, Igor V. Komarov, Yurii S. Moroz, Dmitriy M. Volochnyuk, Pavel K. Mykhailiuk, Anne S. Ulrich, Sergii Afonin, Konstantin Fackeldey, Haribabu Arthanari and Andras Boeszoermenyi and has published in prestigious journals such as Nature, Chemical Reviews and Angewandte Chemie International Edition.

In The Last Decade

Dmytro S. Radchenko

52 papers receiving 1.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

An open-source drug discovery platform enables ultra-large virtual screens

2020 395 citations Christoph Gorgulla, Andras Boeszoermenyi et al. Nature profile →
Synthon-based ligand discovery in virtual libraries of over 11 billion compounds

2021 254 citations Yongfeng Liu, Xi‐Ping Huang et al. Nature profile →

Peers

Countries citing papers authored by Dmytro S. Radchenko

Since Specialization

Citations

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

Fields of papers citing papers by Dmytro S. Radchenko

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dmytro S. Radchenko. 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 Dmytro S. Radchenko. The network helps show where Dmytro S. Radchenko may publish in the future.

Co-authorship network of co-authors of Dmytro S. Radchenko

This figure shows the co-authorship network connecting the top 25 collaborators of Dmytro S. Radchenko. A scholar is included among the top collaborators of Dmytro S. Radchenko 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 Dmytro S. Radchenko. Dmytro S. Radchenko 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	The impact of library size and scale of testing on virtual screening 2025 ·Nature Chemical Biology ·Fangyu Liu, Olivier Mailhot, (unknown), (unknown), (unknown), Xinyu Xu, (unknown), (unknown), Dmytro S. Radchenko, James S. Fraser, Yurii S. Moroz, John J. Irwin, Brian K. Shoichet	12
2	Exploration of structure-activity relationships for the SARS-CoV-2 macrodomain from shape-based fragment linking and active learning 2025 ·Science Advances ·G.J. Correy, (unknown), (unknown), Stefan Gahbauer, (unknown), (unknown), Priyadarshini Jaishankar, (unknown), Brian Goldman, (unknown), (unknown), Dmytro S. Radchenko, Yurii S. Moroz, Alan Ashworth, Patrick Riley, Brian K. Shoichet, Adam R. Renslo, W. Patrick Walters, James S. Fraser	2
3	Expanding chemical space of N-acyl sulfonamides for carbonic anhydrase inhibitor discovery 2025 ·European Journal of Medicinal Chemistry ·(unknown), Bohdan V. Vashchenko, (unknown), (unknown), Olga Kuchuk, (unknown), (unknown), В. С. Броварец, Sergey Zozulya, Dmytro S. Radchenko, Oleksandr O. Grygorenko, Yurii S. Moroz	0
4	A bottom-up approach to find lead compounds in expansive chemical spaces 2025 ·Communications Chemistry ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), C. Iglesias Escudero, Tian V. Tian, (unknown), Dmytro S. Radchenko, Yurii S. Moroz, Lucas A. Defelipe, David Carrillo, María García-Alai, Robert Schmidt, Matthias Rarey, Patrick Aloy, Carles Galdeano, Jordi Juárez‐Jiménez, Xavier Barril	0
5	Ultra-large virtual screening unveils potent agonists of the neuromodulatory orphan receptor GPR139 2025 ·Nature Communications ·Israel Cabeza de Vaca, (unknown), (unknown), Duy Duc Vo, (unknown), (unknown), (unknown), (unknown), (unknown), Aljona Saleh, (unknown), Dmytro S. Radchenko, Yurii S. Moroz, Hans Bräuner‐Osborne, Per Svenningsson, Jan Kihlberg, Zhi‐Jie Liu, Alexander S. Hauser, Jens Carlsson	1
6	Rapid traversal of vast chemical space using machine learning-guided docking screens 2025 ·Nature Computational Science ·Andreas Luttens, Israel Cabeza de Vaca, (unknown), José Brea, (unknown), (unknown), Dmytro S. Radchenko, Yurii S. Moroz, Marı́a Isabel Loza, Ulf Norinder, Jens Carlsson	15
7	S _N Ar or Sulfonylation? Chemoselective Amination of Halo(het)arene Sulfonyl Halides for Synthetic Applications and Ultralarge Compound Library Design 2024 ·The Journal of Organic Chemistry ·(unknown), (unknown), Dmytro S. Radchenko, Dmytro Dudenko, Yurii S. Moroz, Andrey A. Tolmachev, (unknown), Oleksandr O. Grygorenko	2
8	Generation of multimillion chemical space based on the parallel Groebke–Blackburn–Bienaymé reaction 2024 ·Beilstein Journal of Organic Chemistry ·(unknown), (unknown), (unknown), Dmytro S. Radchenko, Dmytro Dudenko, Yurii S. Moroz, O.D. Kachkovsky, Oleksandr O. Grygorenko	1
9	Advancing molecular graphs with descriptors for the prediction of chemical reaction yields 2022 ·Journal of Computational Chemistry ·(unknown), (unknown), Oleksandr O. Grygorenko, Dmytro S. Radchenko, Yurii S. Moroz, (unknown)	14
10	Generative and reinforcement learning approaches for the automated de novo design of bioactive compounds 2022 ·Communications Chemistry ·(unknown), (unknown), Stephen J. Capuzzi, Dmytro S. Radchenko, Olena Savych, (unknown), Carrow I. Wells, Timothy M. Willson, Alexander Tropsha, Olexandr Isayev	59
11	Structures of the σ2 receptor enable docking for bioactive ligand discovery 2021 ·Nature ·Assaf Alon, Jiankun Lyu, João M. Bráz, Tia A. Tummino, Veronica Craik, Matthew J. O’Meara, Chase M. Webb, Dmytro S. Radchenko, Yurii S. Moroz, Xi‐Ping Huang, Yongfeng Liu, Bryan L. Roth, John J. Irwin, Allan I. Basbaum, Brian K. Shoichet, Andrew C. Kruse	135
12	One-pot parallel synthesis of 1,3,5-trisubstituted 1,2,4-triazoles 2021 ·Molecular Diversity ·Dmytro S. Radchenko, (unknown), (unknown), (unknown), K.E. Gubina, Yurii S. Moroz, Oleksandr O. Grygorenko	4
13	An open-source drug discovery platform enables ultra-large virtual screens breakdown → 2020 ·Nature ·Christoph Gorgulla, Andras Boeszoermenyi, Zifu Wang, Patrick D. Fischer, Paul Coote, Krishna Mohan Das, Yehor S. Malets, Dmytro S. Radchenko, Yurii S. Moroz, David A. Scott, Konstantin Fackeldey, Moritz Hoffmann, (unknown), Gerhard Wagner, Haribabu Arthanari	395
14	Generating Multibillion Chemical Space of Readily Accessible Screening Compounds 2020 ·iScience ·Oleksandr O. Grygorenko, Dmytro S. Radchenko, (unknown), Alexander Chuprina, K.E. Gubina, Yurii S. Moroz	125
15	Supreme activity of gramicidin S against resistant, persistent and biofilm cells of staphylococci and enterococci 2019 ·Scientific Reports ·Marina Berditsch, Sergii Afonin, (unknown), (unknown), (unknown), Oleg Babii, Dmytro S. Radchenko, (unknown), (unknown), (unknown), Uwe Strähle, Andrew Nelson, Klára Valkó, Anne S. Ulrich	40
16	Does a methionine-to-norleucine substitution in PGLa influence peptide-membrane interactions? 2016 ·Biochimica et Biophysica Acta (BBA) - Biomembranes ·Dmytro S. Radchenko, (unknown), (unknown), Anne S. Ulrich, Sergii Afonin	17
17	Design, Synthesis, and Application of a Trifluoromethylated Phenylalanine Analogue as a Label to Study Peptides by Solid‐State ¹⁹F NMR Spectroscopy 2013 ·Angewandte Chemie International Edition ·(unknown), Dmytro S. Radchenko, Pavel K. Mykhailiuk, Sergii Afonin, Anne S. Ulrich, Igor V. Komarov	19
18	A ¹⁹F NMR Label to Substitute Polar Amino Acids in Peptides: A CF₃‐Substituted Analogue of Serine and Threonine 2012 ·Angewandte Chemie International Edition ·(unknown), Pavel K. Mykhailiuk, Sergii Afonin, Dmytro S. Radchenko, Vladimir Kubyshkin, Anne S. Ulrich, Igor V. Komarov	41
19	Exploiting the Addition of Trimethyl(trifluoromethyl)silane to Functionalized N-Benzylimines for the Preparation of Two Novel x-Trifluoromethyl x-Amino Acids 2012 ·Synthesis ·Pavel K. Mykhailiuk, (unknown), Dmytro S. Radchenko, Олег В. Шишкин, Andrei A. Tolmachev, Igor V. Komarov	14
20	Synthesis of 2-azaspiro[3.3]heptane-derived amino acids: ornitine and GABA analogues 2010 ·Amino Acids ·Dmytro S. Radchenko, Oleksandr O. Grygorenko, Igor V. Komarov	22

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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