Dao-Feng Chen

599 total citations
13 papers, 541 citations indexed

About

Dao-Feng Chen is a scholar working on Molecular Biology, Pharmacology and Biomaterials. According to data from OpenAlex, Dao-Feng Chen has authored 13 papers receiving a total of 541 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 3 papers in Pharmacology and 2 papers in Biomaterials. Recurrent topics in Dao-Feng Chen's work include Plant-derived Lignans Synthesis and Bioactivity (4 papers), Natural product bioactivities and synthesis (4 papers) and Plant Toxicity and Pharmacological Properties (3 papers). Dao-Feng Chen is often cited by papers focused on Plant-derived Lignans Synthesis and Bioactivity (4 papers), Natural product bioactivities and synthesis (4 papers) and Plant Toxicity and Pharmacological Properties (3 papers). Dao-Feng Chen collaborates with scholars based in China, United States and Taiwan. Dao-Feng Chen's co-authors include Kuo‐Hsiung Lee, Kenneth F. Bastow, Min Chen, Nicole Kilgore, Susan L. Morris‐Natschke, Lan Xie, Ke Chen, Yoshiki Kashiwada, L. Mark Cosentino and Pei Wang and has published in prestigious journals such as Bioorganic & Medicinal Chemistry, Journal of Natural Products and Evidence-based Complementary and Alternative Medicine.

In The Last Decade

Dao-Feng Chen

13 papers receiving 524 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dao-Feng Chen China 10 438 169 100 84 76 13 541
Ih‐Sheng Chen Taiwan 16 272 0.6× 180 1.1× 97 1.0× 92 1.1× 79 1.0× 31 495
Tran Ngoc Ninh Vietnam 18 444 1.0× 202 1.2× 82 0.8× 126 1.5× 136 1.8× 30 699
Christine Kamperdick Germany 14 305 0.7× 180 1.1× 101 1.0× 59 0.7× 54 0.7× 27 447
Etienne Rakotobe United States 17 294 0.7× 189 1.1× 122 1.2× 93 1.1× 43 0.6× 29 512
Hunsa Prawat Thailand 14 270 0.6× 191 1.1× 78 0.8× 122 1.5× 66 0.9× 40 536
Gervais Mouthé Happi Cameroon 15 288 0.7× 211 1.2× 125 1.3× 46 0.5× 100 1.3× 55 473
Troy Smillie United States 16 289 0.7× 179 1.1× 48 0.5× 93 1.1× 81 1.1× 23 602
Rabodo Andriantsiferana United States 17 480 1.1× 219 1.3× 99 1.0× 130 1.5× 49 0.6× 33 749
Wendong Xu China 11 394 0.9× 154 0.9× 46 0.5× 107 1.3× 94 1.2× 17 492
Phan Tông Son Japan 16 424 1.0× 297 1.8× 69 0.7× 54 0.6× 131 1.7× 40 660

Countries citing papers authored by Dao-Feng Chen

Since Specialization
Citations

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

Fields of papers citing papers by Dao-Feng Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Dao-Feng Chen. 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 Dao-Feng Chen. The network helps show where Dao-Feng Chen may publish in the future.

Co-authorship network of co-authors of Dao-Feng Chen

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

All Works

13 of 13 papers shown
1.
Yang, Chen, Yuting Liao, Shiming Yang, et al.. (2025). Site-selective structural modification of toosendanin enables one-step synthesis of 12-hydroxyamoorastatin: A natural tautomeric antitumor lead with low toxicity. Bioorganic Chemistry. 161. 108578–108578. 1 indexed citations
2.
3.
Yan, Min, Yan Lu, Chin‐Ho Chen, et al.. (2015). Stelleralides D–J and Anti-HIV Daphnane Diterpenes from Stellera chamaejasme. Journal of Natural Products. 78(11). 2712–2718. 43 indexed citations
4.
Xia, Long, et al.. (2014). Rabdosia japonicavar.glaucocalyxFlavonoids Fraction Attenuates Lipopolysaccharide‐Induced Acute Lung Injury in Mice. Evidence-based Complementary and Alternative Medicine. 2014(1). 894515–894515. 9 indexed citations
5.
Lu, Yan, et al.. (2013). Cytotoxic and potential anticancer constituents from the stems ofSchisandra pubescens. Pharmaceutical Biology. 51(9). 1204–1207. 5 indexed citations
6.
Chen, Tzu-Hsuan, et al.. (2012). Songaricalarins A–E, Cytotoxic Oplopane Sesquiterpenes from Ligularia songarica. Journal of Natural Products. 76(3). 305–310. 15 indexed citations
7.
Chen, Tzu-Hsuan, et al.. (2010). Altaicalarins A−D, Cytotoxic Bisabolane Sesquiterpenes from Ligularia altaica. Journal of Natural Products. 73(2). 139–142. 25 indexed citations
8.
Mu, Qing, et al.. (2007). Eremophilane Sesquiterpenes fromLigulariamacrophylla. Journal of Natural Products. 70(8). 1259–1262. 34 indexed citations
9.
Chen, Tzu-Hsuan, et al.. (2007). Filiasparosides A−D, Cytotoxic Steroidal Saponins from the Roots of Asparagus filicinus. Journal of Natural Products. 70(8). 1263–1267. 32 indexed citations
10.
Chen, Min, Nicole Kilgore, Kuo‐Hsiung Lee, & Dao-Feng Chen. (2006). Rubrisandrins A and B, Lignans and Related Anti-HIV Compounds from Schisandra rubriflora. Journal of Natural Products. 69(12). 1697–1701. 71 indexed citations
11.
Chen, Lei, et al.. (2004). New Isoprenylated Flavones, Artochamins A−E, and Cytotoxic Principles from Artocarpus chama. Journal of Natural Products. 67(5). 757–761. 78 indexed citations
12.
Chen, Dao-Feng, Mutsuo Kozuka, Feng Ju, et al.. (2002). Interiotherins C and D, Two New Lignans from Kadsura interior and Antitumor-Promoting Effects of Related Neolignans on Epstein−Barr Virus Activation. Journal of Natural Products. 65(9). 1242–1245. 83 indexed citations
13.
Chen, Dao-Feng, Lan Xie, Ke Chen, et al.. (1997). Anti-aids agents—XXVI. Structure-activity correlations of Gomisin-G-related anti-HIV lignans from Kadsura interior and of related synthetic analogues. Bioorganic & Medicinal Chemistry. 5(8). 1715–1723. 144 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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