Xing‐De Wu

1.9k total citations
111 papers, 1.6k citations indexed

About

Xing‐De Wu is a scholar working on Molecular Biology, Plant Science and Pharmacology. According to data from OpenAlex, Xing‐De Wu has authored 111 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 75 papers in Molecular Biology, 42 papers in Plant Science and 38 papers in Pharmacology. Recurrent topics in Xing‐De Wu's work include Natural product bioactivities and synthesis (41 papers), Cholinesterase and Neurodegenerative Diseases (27 papers) and Phytochemistry and Biological Activities (21 papers). Xing‐De Wu is often cited by papers focused on Natural product bioactivities and synthesis (41 papers), Cholinesterase and Neurodegenerative Diseases (27 papers) and Phytochemistry and Biological Activities (21 papers). Xing‐De Wu collaborates with scholars based in China and United States. Xing‐De Wu's co-authors include Qin‐Shi Zhao, Li‐Yan Peng, Juan He, Liao‐Bin Dong, Jia Su, Liu‐Dong Song, Lin‐Fen Ding, Xiao Cheng, Juan He and Xiao‐Nian Li and has published in prestigious journals such as Chemical Communications, Food Chemistry and The Journal of Organic Chemistry.

In The Last Decade

Xing‐De Wu

110 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Xing‐De Wu China 23 915 488 483 405 214 111 1.6k
Li‐Yan Peng China 23 1.2k 1.4× 518 1.1× 809 1.7× 432 1.1× 295 1.4× 128 2.0k
Shi‐Shan Yu China 25 1.1k 1.3× 509 1.0× 577 1.2× 447 1.1× 287 1.3× 108 1.9k
Yegao Chen China 21 982 1.1× 576 1.2× 716 1.5× 221 0.5× 240 1.1× 175 1.6k
Mi Hee Woo South Korea 25 1.1k 1.2× 454 0.9× 461 1.0× 216 0.5× 248 1.2× 94 1.9k
Yong‐Xian Cheng China 27 723 0.8× 843 1.7× 413 0.9× 338 0.8× 455 2.1× 84 1.7k
Shepo Shi China 29 1.3k 1.4× 473 1.0× 664 1.4× 538 1.3× 213 1.0× 107 2.2k
Jun‐Mian Tian China 26 977 1.1× 369 0.8× 504 1.0× 334 0.8× 177 0.8× 76 1.6k
Trần Mạnh Hưng South Korea 24 990 1.1× 449 0.9× 537 1.1× 213 0.5× 244 1.1× 52 1.8k
Shih‐Chang Chien Taiwan 23 723 0.8× 388 0.8× 433 0.9× 255 0.6× 208 1.0× 62 1.5k
Da‐Yuan Zhu China 20 683 0.7× 425 0.9× 458 0.9× 246 0.6× 147 0.7× 72 1.3k

Countries citing papers authored by Xing‐De Wu

Since Specialization
Citations

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

Fields of papers citing papers by Xing‐De Wu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Xing‐De Wu. 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 Xing‐De Wu. The network helps show where Xing‐De Wu may publish in the future.

Co-authorship network of co-authors of Xing‐De Wu

This figure shows the co-authorship network connecting the top 25 collaborators of Xing‐De Wu. A scholar is included among the top collaborators of Xing‐De Wu 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 Xing‐De Wu. Xing‐De Wu 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.
Wang, Haiyin, et al.. (2024). Clerodane diterpenoids from the vine stems of Fibraurea recisa Pierre and their hepatic gluconeogenesis inhibitory activity. Phytochemistry. 232. 114364–114364. 1 indexed citations
3.
Ding, Lin‐Fen, et al.. (2023). Eudesmane-type sesquiterpenoids from the aerial parts of Artemisia lavandulaefolia and their anti-pancreatic cancer activities. Phytochemistry. 216. 113871–113871. 3 indexed citations
4.
Wu, Xing‐De, et al.. (2022). Design, synthesis and structural-activity relationship studies of phanginin A derivatives for regulating SIK1-cAMP/CREB signaling to suppress hepatic gluconeogenesis. European Journal of Medicinal Chemistry. 232. 114171–114171. 9 indexed citations
5.
Ding, Lin‐Fen, et al.. (2021). Cassane diterpenoids from the seeds of Caesalpinia bonduc and their nitric oxide production and α-glucosidase inhibitory activities. Phytochemistry. 193. 112973–112973. 13 indexed citations
6.
Liu, Jiangxin, et al.. (2021). Discovery of pseudolaric acid A as a new Hsp90 inhibitor uncovers its potential anticancer mechanism. Bioorganic Chemistry. 112. 104963–104963. 14 indexed citations
7.
Zhu, Qin‐Feng, Li‐Dong Shao, Xing‐De Wu, Jiangxin Liu, & Qin‐Shi Zhao. (2019). Isolation, Structural Assignment of Isoselagintamarlin A from Selaginella tamariscina and Its Biomimetic Synthesis. Natural Products and Bioprospecting. 9(1). 69–74. 9 indexed citations
8.
Qi, Yanyan, Lin‐Fen Ding, Hui Yang, et al.. (2019). Diterpenoids and sesquiterpenoids from the stem bark of Metasequoia glyptostroboides. Phytochemistry. 161. 86–96. 13 indexed citations
9.
Ding, Lin‐Fen, Jia Su, Zheng‐Hong Pan, et al.. (2018). Cytotoxic sesquiterpenoids from the leaves of Magnolia grandiflora. Phytochemistry. 155. 182–190. 27 indexed citations
10.
Zhang, Zhi‐Jun, Yin Nian, Qin‐Feng Zhu, et al.. (2017). Lycoplanine A, a C16N Lycopodium Alkaloid with a 6/9/5 Tricyclic Skeleton from Lycopodium complanatum. Organic Letters. 19(17). 4668–4671. 29 indexed citations
11.
Gao, Xiu, Juan He, Xing‐De Wu, et al.. (2016). Sauruchinenols A and B, unprecedented monocyclic diterpenes with new carbon skeleton from the aerial parts of Saururus chinensis. Fitoterapia. 116. 116–120. 7 indexed citations
12.
Fan, Min, Juan He, Xing‐De Wu, et al.. (2015). New cytotoxic and anti-inflammatory compounds isolated fromMorus albaL.. Natural Product Research. 29(18). 1711–1718. 35 indexed citations
13.
He, Juan, et al.. (2014). Isolation, characterisation, and antioxidant activities of flavonoids from chufa (Eleocharis tuberosa) peels. Food Chemistry. 164. 30–35. 27 indexed citations
14.
Jiang, Weiwei, Fei Liu, Xiu Gao, et al.. (2014). Huperserines A–E, Lycopodium alkaloids from Huperzia serrata. Fitoterapia. 99. 72–77. 17 indexed citations
15.
Jiang, Weiwei, Jia Su, Xing‐De Wu, et al.. (2014). Geissoschizine methyl etherN-oxide, a new alkaloid with antiacetylcholinesterase activity fromUncaria rhynchophylla. Natural Product Research. 29(9). 842–847. 24 indexed citations
16.
He, Juan, Xing‐De Wu, Fei Liu, et al.. (2014). Lycopodine-Type Alkaloids from Lycopodium japonicum. Natural Products and Bioprospecting. 4(4). 213–219. 11 indexed citations
17.
Wu, Xing‐De, Shuangyan Wang, Lei Wang, et al.. (2013). Labdane diterpenoids and lignans from Calocedrus macrolepis. Fitoterapia. 85. 154–160. 10 indexed citations
18.
Wu, Xing‐De, Jin‐Tang Cheng, Juan He, et al.. (2012). Benzophenone glycosides and epicatechin derivatives from Malania oleifera. Fitoterapia. 83(6). 1068–1071. 14 indexed citations
19.
Pan, Zheng‐Hong, et al.. (2012). A cytotoxic cardenolide and a saponin from the rhizomes of Tupistra chinensis. Fitoterapia. 83(8). 1489–1493. 28 indexed citations
20.
Pan, Zheng‐Hong, Yan Li, Xing‐De Wu, et al.. (2012). Norditerpenoids from Salvia castanea Diels f. pubescens. Fitoterapia. 83(6). 1072–1075. 17 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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