Chang‐Qi Hu

1.1k total citations
30 papers, 916 citations indexed

About

Chang‐Qi Hu is a scholar working on Molecular Biology, Organic Chemistry and Plant Science. According to data from OpenAlex, Chang‐Qi Hu has authored 30 papers receiving a total of 916 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 9 papers in Organic Chemistry and 9 papers in Plant Science. Recurrent topics in Chang‐Qi Hu's work include Natural product bioactivities and synthesis (12 papers), Sirtuins and Resveratrol in Medicine (6 papers) and Phytochemistry and Biological Activities (6 papers). Chang‐Qi Hu is often cited by papers focused on Natural product bioactivities and synthesis (12 papers), Sirtuins and Resveratrol in Medicine (6 papers) and Phytochemistry and Biological Activities (6 papers). Chang‐Qi Hu collaborates with scholars based in China, United States and Japan. Chang‐Qi Hu's co-authors include Hui‐Kang Wang, Junko Ishida, Qian Shi, Robert E. Kilkuskie, Ke Chen, Kuo‐Hsiung Lee, Kenneth F. Bastow, Kuo-Hsiung Lee, Ping Zhang and Yung‐Chi Cheng and has published in prestigious journals such as Tetrahedron, Journal of Ethnopharmacology and Bioorganic & Medicinal Chemistry.

In The Last Decade

Chang‐Qi Hu

30 papers receiving 884 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Chang‐Qi Hu China 14 574 249 202 139 104 30 916
Magnus A. Azuine United States 13 402 0.7× 248 1.0× 229 1.1× 145 1.0× 70 0.7× 17 1.1k
Michael Hawthorne United States 20 784 1.4× 292 1.2× 278 1.4× 117 0.8× 53 0.5× 27 1.4k
Masayoshi Oyama Japan 22 683 1.2× 290 1.2× 344 1.7× 190 1.4× 92 0.9× 73 1.4k
Do Thi Ha South Korea 20 549 1.0× 157 0.6× 302 1.5× 145 1.0× 141 1.4× 61 1.1k
Yean‐Jang Lee Taiwan 20 440 0.8× 391 1.6× 173 0.9× 223 1.6× 72 0.7× 41 1.2k
Kuo-Hsiung Lee United States 23 735 1.3× 389 1.6× 196 1.0× 142 1.0× 135 1.3× 50 1.3k
Albert J. Chulia France 22 956 1.7× 156 0.6× 599 3.0× 111 0.8× 150 1.4× 67 1.5k
Kanaya Lal Dhar India 21 529 0.9× 303 1.2× 219 1.1× 125 0.9× 128 1.2× 36 1.0k
Ken‐ichi Nakaya Japan 20 693 1.2× 272 1.1× 401 2.0× 155 1.1× 66 0.6× 43 1.3k
Vernon E. Steele United States 17 502 0.9× 108 0.4× 96 0.5× 148 1.1× 43 0.4× 20 981

Countries citing papers authored by Chang‐Qi Hu

Since Specialization
Citations

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

Fields of papers citing papers by Chang‐Qi Hu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chang‐Qi Hu. 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 Chang‐Qi Hu. The network helps show where Chang‐Qi Hu may publish in the future.

Co-authorship network of co-authors of Chang‐Qi Hu

This figure shows the co-authorship network connecting the top 25 collaborators of Chang‐Qi Hu. A scholar is included among the top collaborators of Chang‐Qi Hu 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 Chang‐Qi Hu. Chang‐Qi Hu 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.
Hu, Chang‐Qi, et al.. (2007). X‐Ray Crystal Structure and Antioxidant Activity of Salidroside, a Phenylethanoid Glycoside. Chemistry & Biodiversity. 4(3). 508–513. 45 indexed citations
2.
Gai, Yue, Lingling Zhao, Chang‐Qi Hu, & Huiping Zhang. (2007). Roridin H. Acta Crystallographica Section E Structure Reports Online. 63(6). o2990–o2991. 2 indexed citations
3.
Yang, Guo‐Xun, et al.. (2007). [Anti-HIV chemical constituents of aerial parts of Caragana rosea].. Yaoxue xuebao. 42(2). 179–82. 5 indexed citations
4.
Mu, Qing, Simon Gibbons, Michael Stavri, et al.. (2006). Antibacterial Effects ofHypericum ascyron. andHypericum japonicum. Against Multidrug-ResistantStaphylococcus aureus.. Pharmaceutical Biology. 44(3). 157–159. 6 indexed citations
5.
Sun, Xun, Kenji Izumi, Chang‐Qi Hu, & Guo‐Qiang Lin. (2006). Convenient Synthesis of Indene Derivatives via Intramolecular Friedel-Crafts Cyclization of Tetraaryl Substituted 1,3-Butadienes. Chinese Journal of Chemistry. 24(3). 430–434. 23 indexed citations
6.
Sun, Xun, Kenji Izumi, Chang‐Qi Hu, & Guo‐Qiang Lin. (2006). Convenient Synthesis of Indene Derivatives via Intramolecular Friedel—Crafts Cyclization of Tetraaryl Substituted 1,3‐Butadienes.. ChemInform. 37(28). 1 indexed citations
7.
Liang, Gaolin, Jing Bi, Hong Huang, Su Zhang, & Chang‐Qi Hu. (2005). Metabolites and the pharmacokinetics of kobophenol A from Caragana sinica in rats. Journal of Ethnopharmacology. 101(1-3). 324–329. 6 indexed citations
8.
Yang, Guo‐Xun, et al.. (2005). Anti-HIV Bioactive Stilbene Dimers ofCaragana rosea. Planta Medica. 71(6). 569–571. 29 indexed citations
9.
Wang, Shuguang, Da‐You Ma, & Chang‐Qi Hu. (2004). Two new oligostilbenes from Caragana sinica. Journal of Asian Natural Products Research. 6(4). 241–248. 13 indexed citations
10.
Sun, Zhihua, Bo Chen, Su Zhang, & Chang‐Qi Hu. (2004). Four New Eudesmanes from Caragana intermedia and Their Biological Activities. Journal of Natural Products. 67(12). 1975–1979. 55 indexed citations
11.
Chen, Gang, et al.. (2001). Identification and Determination of Oligomeric Stilbenes in the Roots of Caragana Species by Capillary Electrophoresis. Planta Medica. 67(7). 665–668. 13 indexed citations
12.
Zhang, Ping, et al.. (2001). Five novel oligostilbenes from the roots of Caragana sinica. Tetrahedron. 57(23). 4849–4854. 80 indexed citations
13.
Ishida, Junko, Hui‐Kang Wang, Masayoshi Oyama, et al.. (2001). Anti-AIDS Agents. 46. Anti-HIV Activity of Harman, an Anti-HIV Principle from Symplocos setchuensis, and Its Derivatives. Journal of Natural Products. 64(7). 958–960. 111 indexed citations
14.
Ishida, Junko, Hui‐Kang Wang, Kenneth F. Bastow, Chang‐Qi Hu, & Kuo-Hsiung Lee. (1999). Antitumor agents 201.1 Cytotoxicity of harmine and β-carboline analogs. Bioorganic & Medicinal Chemistry Letters. 9(23). 3319–3324. 139 indexed citations
15.
Chen, Ke, Qian Shi, Toshihiro Fujioka, et al.. (1995). Anti-AIDS agents—XIX. Neotripterifordin, a novel anti-HIV principle from Tripterygium wilfordii: Isolation and structural elucidation. Bioorganic & Medicinal Chemistry. 3(10). 1345–1348. 38 indexed citations
16.
Kulanthaivel, Palaniappan, et al.. (1995). Naturally Occurring Protein Kinase C Inhibitors; II1. Isolation of Oligomeric Stilbenes fromCaragana sinica2. Planta Medica. 61(1). 41–44. 35 indexed citations
17.
Hu, Chang‐Qi, Ke Chen, Qian Shi, et al.. (1994). Anti-AIDS Agents, 10. Acacetin-7-O-β-D-galactopyranoside, an Anti-HIV Principle from Chrysanthemum morifolium and a Structure-Activity Correlation with Some Related Flavonoids. Journal of Natural Products. 57(1). 42–51. 135 indexed citations
18.
Chen, Ke, Qian Shi, Yoshiki Kashiwada, et al.. (1992). Anti-AIDS Agents, 6. Salaspermic Acid, an Anti-HIV Principle from Tripterycium wilfordii, and the Structure-activity Correlation with its Related Compounds. Journal of Natural Products. 55(3). 340–346. 37 indexed citations
19.
Chen, Ke, Qian Shi, Toshihiro Fujioka, et al.. (1992). Anti-AIDS Agents, 4. Tripterifordin, a Novel Anti-HIV Principle from Tripterygium wilfordii: Isolation and Structural Elucidation. Journal of Natural Products. 55(1). 88–92. 55 indexed citations
20.
Hu, Chang‐Qi, Jerjang Chang, & Kuo‐Hsiung Lee. (1990). Antitumor Agents, 115. Seselidiol, a New Cytotoxic Polyacetylene from Sesli mairei. Journal of Natural Products. 53(4). 932–935. 31 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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