Bing‐Xin Zhao

1.1k total citations
53 papers, 965 citations indexed

About

Bing‐Xin Zhao is a scholar working on Biotechnology, Organic Chemistry and Pharmacology. According to data from OpenAlex, Bing‐Xin Zhao has authored 53 papers receiving a total of 965 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Biotechnology, 23 papers in Organic Chemistry and 19 papers in Pharmacology. Recurrent topics in Bing‐Xin Zhao's work include Marine Sponges and Natural Products (27 papers), Microbial Natural Products and Biosynthesis (16 papers) and Chemical synthesis and alkaloids (13 papers). Bing‐Xin Zhao is often cited by papers focused on Marine Sponges and Natural Products (27 papers), Microbial Natural Products and Biosynthesis (16 papers) and Chemical synthesis and alkaloids (13 papers). Bing‐Xin Zhao collaborates with scholars based in China, Hong Kong and United States. Bing‐Xin Zhao's co-authors include Ying Wang, Wen‐Cai Ye, Shi‐Hai Xu, Xiao‐Jun Huang, Xiaojian Liao, Dongmei Zhang, Nan Ma, Ren‐Wang Jiang, Wei‐Min Chen and Guo‐Cai Wang and has published in prestigious journals such as Angewandte Chemie International Edition, Chemical Communications and Journal of Agricultural and Food Chemistry.

In The Last Decade

Bing‐Xin Zhao

51 papers receiving 947 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Bing‐Xin Zhao China 18 405 273 271 261 244 53 965
Rui‐Yun Yang China 21 160 0.4× 561 2.1× 305 1.1× 486 1.9× 162 0.7× 80 1.3k
Kuo Xu China 20 165 0.4× 280 1.0× 163 0.6× 466 1.8× 135 0.6× 68 1.1k
Akemi Umeyama Japan 23 309 0.8× 344 1.3× 321 1.2× 608 2.3× 265 1.1× 95 1.5k
Tung-Ying Wu Taiwan 17 157 0.4× 359 1.3× 93 0.3× 437 1.7× 158 0.6× 25 915
Yue‐Hu Pei China 19 151 0.4× 297 1.1× 181 0.7× 570 2.2× 101 0.4× 76 1.0k
Zhongbin Cheng China 21 166 0.4× 499 1.8× 357 1.3× 340 1.3× 79 0.3× 52 862
You‐Min Ying China 19 179 0.4× 570 2.1× 198 0.7× 480 1.8× 98 0.4× 76 1.0k
Jong-Pyung Kim South Korea 18 234 0.6× 347 1.3× 98 0.4× 365 1.4× 71 0.3× 29 890
Noboru Shoji Japan 21 216 0.5× 200 0.7× 210 0.8× 398 1.5× 261 1.1× 53 1.0k
Changxing Qi China 21 252 0.6× 796 2.9× 338 1.2× 565 2.2× 120 0.5× 95 1.3k

Countries citing papers authored by Bing‐Xin Zhao

Since Specialization
Citations

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

Fields of papers citing papers by Bing‐Xin Zhao

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bing‐Xin Zhao. 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 Bing‐Xin Zhao. The network helps show where Bing‐Xin Zhao may publish in the future.

Co-authorship network of co-authors of Bing‐Xin Zhao

This figure shows the co-authorship network connecting the top 25 collaborators of Bing‐Xin Zhao. A scholar is included among the top collaborators of Bing‐Xin Zhao 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 Bing‐Xin Zhao. Bing‐Xin Zhao 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.
Yuan, Yuan, et al.. (2025). Bioactive Terpenes from Marine Sponges and Their Associated Organisms. Marine Drugs. 23(3). 96–96. 1 indexed citations
3.
Liao, Xiaojian, et al.. (2023). Isolation and total synthesis of dysidone A: a new piperidone alkaloid from the marine sponge Dysidea sp.. RSC Advances. 13(42). 29316–29319. 3 indexed citations
4.
Liu, Tingting, et al.. (2023). A new chlorobenzoate derivative from the red alga Solieria sp.. Journal of Asian Natural Products Research. 25(9). 899–904. 1 indexed citations
5.
Liao, Xiaojian, et al.. (2022). Synthesis of Marine Cyclopeptide Galaxamide Analogues as Potential Anticancer Agents. Marine Drugs. 20(3). 158–158. 8 indexed citations
6.
Chen, Guo‐Dong, Bing‐Xin Zhao, Meijuan Huang, et al.. (2021). Tripodalsporormielones A–C, unprecedented cage-like polyketides with complex polyvdent bridged and fused ring systems. Acta Pharmaceutica Sinica B. 11(11). 3648–3654. 9 indexed citations
7.
Liu, Tingting, Xiaojian Liao, Shi‐Hai Xu, & Bing‐Xin Zhao. (2020). Solieritide A, a new polyketide from the red alga Solieria sp. Natural Product Research. 35(21). 3780–3786. 12 indexed citations
8.
Zhou, Rong, Xiaojian Liao, Jing Li, et al.. (2018). Isolation and Synthesis of Misszrtine A: A Novel Indole Alkaloid From Marine Sponge-Associated Aspergillus sp. SCSIO XWS03F03. Frontiers in Chemistry. 6. 212–212. 22 indexed citations
9.
Wang, Junfeng, Zhen Wang, Xiuping Lin, et al.. (2017). Structurally diverse secondary metabolites from a deep-sea-derived fungus Penicillium chrysogenum SCSIO 41001 and their biological evaluation. Fitoterapia. 117. 71–78. 50 indexed citations
10.
Liao, Xiaojian, et al.. (2017). Cytotoxicity Study of Cyclopentapeptide Analogues of Marine Natural Product Galaxamide towards Human Breast Cancer Cells. Oxidative Medicine and Cellular Longevity. 2017(1). 8392035–8392035. 15 indexed citations
12.
Tang, Genyun, Xin Liu, Nan Ma, et al.. (2016). Design and Synthesis of Dimeric Securinine Analogues with Neuritogenic Activities. ACS Chemical Neuroscience. 7(10). 1442–1451. 20 indexed citations
13.
Jian, Yuqing, Xiao‐Jun Huang, Dongmei Zhang, et al.. (2015). Guapsidial A and Guadials B and C: Three New Meroterpenoids with Unusual Skeletons from the Leaves of Psidium guajava. Chemistry - A European Journal. 21(25). 9022–9027. 46 indexed citations
14.
Ma, Nan, et al.. (2015). The application of click chemistry in the synthesis of agents with anticancer activity. Drug Design Development and Therapy. 9. 1585–1585. 50 indexed citations
15.
Huang, Xiao‐Jun, Bing‐Xin Zhao, Yuqing Jian, et al.. (2014). Five New Acylphloroglucinol Glycosides from the Leaves of Eucalyptus robusta. Natural Product Communications. 9(2). 209–12. 1 indexed citations
16.
Ma, Nan, Yiwu Yao, Bing‐Xin Zhao, et al.. (2014). Total synthesis of securinega alkaloids (−)-norsecurinine, (−)-niruroidine and (−)-flueggine A. Chemical Communications. 50(66). 9284–9287. 55 indexed citations
17.
Wu, Zhen‐Long, Bing‐Xin Zhao, Xiao‐Jun Huang, et al.. (2014). Suffrutines A and B: A Pair of Z/E Isomeric Indolizidine Alkaloids from the Roots of Flueggea suffruticosa. Angewandte Chemie International Edition. 53(23). 5796–5799. 36 indexed citations
18.
Zhao, Bing‐Xin, Ying Wang, Chen Li, et al.. (2013). Flueggedine, a novel axisymmetric indolizidine alkaloid dimer from Flueggea virosa. Tetrahedron Letters. 54(35). 4708–4711. 45 indexed citations
19.
Chen, Lili, et al.. (2013). Five new stilbene glycosides from the roots of Polygonum multiflorum. Journal of Asian Natural Products Research. 15(11). 1145–1151. 9 indexed citations
20.
Zhao, Bing‐Xin, Ying Wang, Dongmei Zhang, et al.. (2012). Virosaines A and B, Two New Birdcage-Shaped Securinega Alkaloids with an Unprecedented Skeleton from Flueggea virosa. Organic Letters. 14(12). 3096–3099. 65 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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