Duo‐Zhi Chen

653 total citations
35 papers, 525 citations indexed

About

Duo‐Zhi Chen is a scholar working on Molecular Biology, Pharmacology and Organic Chemistry. According to data from OpenAlex, Duo‐Zhi Chen has authored 35 papers receiving a total of 525 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 14 papers in Pharmacology and 9 papers in Organic Chemistry. Recurrent topics in Duo‐Zhi Chen's work include Phytochemical compounds biological activities (9 papers), Chemical synthesis and alkaloids (8 papers) and Phytochemistry and Bioactivity Studies (6 papers). Duo‐Zhi Chen is often cited by papers focused on Phytochemical compounds biological activities (9 papers), Chemical synthesis and alkaloids (8 papers) and Phytochemistry and Bioactivity Studies (6 papers). Duo‐Zhi Chen collaborates with scholars based in China, United Kingdom and Switzerland. Duo‐Zhi Chen's co-authors include Xiao‐Jiang Hao, Ying‐Tong Di, Yu Zhang, Shun‐Lin Li, Jieyun Cai, Hongping He, Gui‐Hua Tang, Chun‐Mao Yuan, Mingming Cao and Chenxu Jing and has published in prestigious journals such as Scientific Reports, The Journal of Organic Chemistry and Molecules.

In The Last Decade

Duo‐Zhi Chen

33 papers receiving 520 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Duo‐Zhi Chen China 16 314 162 161 104 102 35 525
Alex K. Machocho Kenya 14 145 0.5× 227 1.4× 219 1.4× 62 0.6× 194 1.9× 37 587
Clemens A. J. Erdelmeier United States 14 280 0.9× 104 0.6× 119 0.7× 51 0.5× 226 2.2× 23 631
Wiwied Ekasari Indonesia 16 355 1.1× 177 1.1× 215 1.3× 129 1.2× 326 3.2× 60 854
Mikhail D. Antoun United States 13 184 0.6× 98 0.6× 94 0.6× 63 0.6× 171 1.7× 24 446
Ashraf Hamed Egypt 14 166 0.5× 58 0.4× 90 0.6× 83 0.8× 182 1.8× 73 558
Jan H. Wisse United States 15 441 1.4× 142 0.9× 67 0.4× 114 1.1× 257 2.5× 19 687
John M. Pezzuto United States 8 227 0.7× 61 0.4× 74 0.5× 57 0.5× 176 1.7× 8 410
Manik Das India 9 187 0.6× 141 0.9× 76 0.5× 77 0.7× 109 1.1× 21 517
Sianne Schwikkard United Kingdom 12 237 0.8× 123 0.8× 81 0.5× 56 0.5× 190 1.9× 28 560
Anita Mahapatra India 14 262 0.8× 71 0.4× 107 0.7× 101 1.0× 241 2.4× 33 654

Countries citing papers authored by Duo‐Zhi Chen

Since Specialization
Citations

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

Fields of papers citing papers by Duo‐Zhi Chen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Duo‐Zhi 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 Duo‐Zhi Chen. The network helps show where Duo‐Zhi Chen may publish in the future.

Co-authorship network of co-authors of Duo‐Zhi Chen

This figure shows the co-authorship network connecting the top 25 collaborators of Duo‐Zhi Chen. A scholar is included among the top collaborators of Duo‐Zhi 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 Duo‐Zhi Chen. Duo‐Zhi Chen 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.
Ren, Juan, Jieyun Cai, Ting Ruan, et al.. (2024). Potential SARS-CoV-2 Mpro steroid inhibitors from Aphanamixis polystachya (Wall.) R. N. Parker. Fitoterapia. 177. 106134–106134.
2.
Xu, Lili, Duo‐Zhi Chen, Yu Zhang, et al.. (2024). Daphmacrimines A−K, Daphniphyllum alkaloids from Daphniphyllum macropodum Miq. Phytochemistry. 223. 114106–114106. 2 indexed citations
3.
Ruan, Ting, Juan Ren, Qian Zhao, et al.. (2024). Diterpenoids target SARS-CoV-2 RdRp from the roots of Euphorbia fischeriana Steud. Frontiers in Plant Science. 15. 1425759–1425759.
4.
Ren, Juan, Ting Ruan, Yuan Chen, et al.. (2024). Utilizing artificial intelligence for precision exploration of N protein targeting phenanthridine sars-cov-2 inhibitors: A novel approach. European Journal of Medicinal Chemistry. 279. 116885–116885. 1 indexed citations
5.
Hou, Li, Chun‐Mao Yuan, Gui‐Hua Tang, et al.. (2023). Five new limonoids isolated from Walsura robusta. Natural Products and Bioprospecting. 13(1). 7–7. 3 indexed citations
6.
Wang, Yi‐Ting, Xiao Ding, Jieyun Cai, et al.. (2021). Novel nucleocapsid protein-targeting phenanthridine inhibitors of SARS-CoV-2. European Journal of Medicinal Chemistry. 227. 113966–113966. 27 indexed citations
7.
Yuan, Wenjuan, Jiangyu Zhao, Yu Zhang, et al.. (2020). Diterpenes with potential treatment of vitiligo from the aerials parts of Euphorbia antiquorum L. Fitoterapia. 144. 104583–104583. 11 indexed citations
8.
Chen, Duo‐Zhi, et al.. (2018). Anti-TMV Effects of Amaryllidaceae Alkaloids Isolated from the Bulbs of Lycoris radiata and Lycoricidine Derivatives. Natural Products and Bioprospecting. 8(3). 189–197. 12 indexed citations
9.
Yi, Ping, Wei Gu, Chunxia Xiao, et al.. (2018). Hypermonins A and B, two 6-norpolyprenylated acylphloroglucinols with unprecedented skeletons from Hypericum monogynum. Organic & Biomolecular Chemistry. 16(22). 4195–4198. 21 indexed citations
10.
Yuan, Wenjuan, Xiao Ding, Zhe Wang, et al.. (2017). Two novel diterpenoid heterodimers, Bisebracteolasins A and B, from Euphorbia ebracteolata Hayata, and the cancer chemotherapeutic potential of Bisebracteolasin A. Scientific Reports. 7(1). 14507–14507. 21 indexed citations
11.
Yuan, Wenjuan, Shuai Zhang, Pei Cao, et al.. (2017). (±)-Perforison A, A Pair of New Chromone Enantiomers from Harrisonia perforata. Natural Product Communications. 12(1). 63–65. 6 indexed citations
12.
Yuan, Wenjuan, Guo‐Ping Yang, Shuai Zhang, et al.. (2016). Three new diterpenes with cytotoxic activity from the roots of Euphorbia ebracteolata Hayata. Phytochemistry Letters. 18. 176–179. 22 indexed citations
13.
Zhang, Jiahui, Jingjing Guo, Yan-Hui Fu, et al.. (2016). Four new tetracyclic alkaloids with cis-decahydroquinoline motif from Myrioneuron effusum. Fitoterapia. 112. 217–221. 10 indexed citations
14.
Zhang, Yu, Xiaonan Wang, He‐Ping Chen, et al.. (2015). Chemical Constituents from the Stems of Manihot esculenta. Natural Products and Bioprospecting. 5(1). 55–59. 4 indexed citations
15.
Cai, Jieyun, Duo‐Zhi Chen, Yu Zhang, et al.. (2014). Aphanamixis polystachya(センダン科)からのリモノイド類とそれらの摂食阻害活性. Journal of Natural Products. 77(3). 472–482. 1 indexed citations
16.
Huang, Li, Hong‐Chun Liu, Duo‐Zhi Chen, et al.. (2014). Spiramine derivatives induce apoptosis of Bax/Bak cell and cancer cells. Bioorganic & Medicinal Chemistry Letters. 24(8). 1884–1888. 15 indexed citations
17.
Zhang, Yu, Hongping He, Shi-Fei Li, et al.. (2013). A new Amaryllidaceae alkaloid from the bulbs of Lycoris radiata. Chinese Journal of Natural Medicines. 11(4). 406–410. 20 indexed citations
18.
Chen, Duo‐Zhi, Jian‐Dong Jiang, Keqing Zhang, et al.. (2013). Evaluation of anti-HCV activity and SAR study of (+)-lycoricidine through targeting of host heat-stress cognate 70 (Hsc70). Bioorganic & Medicinal Chemistry Letters. 23(9). 2679–2682. 21 indexed citations
19.
Cai, Jieyun, Duo‐Zhi Chen, Shi‐Hong Luo, et al.. (2013). Limonoids from Aphanamixis polystachya and Their Antifeedant Activity. Journal of Natural Products. 77(3). 472–482. 34 indexed citations
20.
Chen, Duo‐Zhi, Jian Yang, Bo Yang, Yuanshuang Wu, & Ting Wu. (2010). Total synthesis of baicalein. Journal of Asian Natural Products Research. 12(2). 124–128. 20 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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