Kan’ichiro Ishiuchi

1.4k total citations
60 papers, 1.1k citations indexed

About

Kan’ichiro Ishiuchi is a scholar working on Pharmacology, Molecular Biology and Plant Science. According to data from OpenAlex, Kan’ichiro Ishiuchi has authored 60 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Pharmacology, 22 papers in Molecular Biology and 17 papers in Plant Science. Recurrent topics in Kan’ichiro Ishiuchi's work include Cholinesterase and Neurodegenerative Diseases (21 papers), Botanical Research and Chemistry (13 papers) and Chemical synthesis and alkaloids (13 papers). Kan’ichiro Ishiuchi is often cited by papers focused on Cholinesterase and Neurodegenerative Diseases (21 papers), Botanical Research and Chemistry (13 papers) and Chemical synthesis and alkaloids (13 papers). Kan’ichiro Ishiuchi collaborates with scholars based in Japan, Malaysia and Taiwan. Kan’ichiro Ishiuchi's co-authors include Jun’ichi Kobayashi, Takaaki Kubota, Toshiaki Makino, Kinya Hotta, Kenji Watanabe, Norimichi Nakahata, Yutaro Obara, Takehito Nakazawa, Hiroshi Noguchi and Shigeki Hayashi and has published in prestigious journals such as Journal of the American Chemical Society, Scientific Reports and Tetrahedron.

In The Last Decade

Kan’ichiro Ishiuchi

54 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kan’ichiro Ishiuchi Japan 22 692 406 399 279 198 60 1.1k
He‐Ping Chen China 20 834 1.2× 486 1.2× 200 0.5× 227 0.8× 169 0.9× 85 1.1k
Jun‐Mian Tian China 26 369 0.5× 977 2.4× 334 0.8× 504 1.8× 177 0.9× 76 1.6k
Yong‐Xian Cheng China 27 843 1.2× 723 1.8× 338 0.8× 413 1.5× 455 2.3× 84 1.7k
Da‐Le Guo China 18 316 0.5× 454 1.1× 141 0.4× 256 0.9× 121 0.6× 94 937
You‐Min Ying China 19 570 0.8× 480 1.2× 179 0.4× 196 0.7× 98 0.5× 76 1.0k
Xing‐De Wu China 23 488 0.7× 915 2.3× 405 1.0× 483 1.7× 214 1.1× 111 1.6k
Sheng‐Zhuo Huang China 18 320 0.5× 433 1.1× 205 0.5× 239 0.9× 197 1.0× 82 880
Weifa Zheng China 20 514 0.7× 347 0.9× 174 0.4× 307 1.1× 94 0.5× 55 1.0k
Zhong‐Duo Yang China 19 397 0.6× 290 0.7× 267 0.7× 158 0.6× 167 0.8× 63 873
Hsun‐Shuo Chang Taiwan 23 313 0.5× 780 1.9× 191 0.5× 361 1.3× 190 1.0× 123 1.5k

Countries citing papers authored by Kan’ichiro Ishiuchi

Since Specialization
Citations

This map shows the geographic impact of Kan’ichiro Ishiuchi'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 Kan’ichiro Ishiuchi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kan’ichiro Ishiuchi more than expected).

Fields of papers citing papers by Kan’ichiro Ishiuchi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kan’ichiro Ishiuchi. 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 Kan’ichiro Ishiuchi. The network helps show where Kan’ichiro Ishiuchi may publish in the future.

Co-authorship network of co-authors of Kan’ichiro Ishiuchi

This figure shows the co-authorship network connecting the top 25 collaborators of Kan’ichiro Ishiuchi. A scholar is included among the top collaborators of Kan’ichiro Ishiuchi 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 Kan’ichiro Ishiuchi. Kan’ichiro Ishiuchi 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.
Saito, Tetsuo, et al.. (2025). Stereoisomerism at the 3-position of glycyrrhetinic acid affects pseudoaldosteronism-related toxicokinetics. Drug Metabolism and Disposition. 53(11). 100180–100180.
2.
Ishiuchi, Kan’ichiro, Tetsuhiro Yoshino, Keiko Ogawa‐Ochiai, et al.. (2024). 3-epi-18β-Glycyrrhetinic Acid or Its Glucuronide, the Metabolites of Glycyrrhizinic Acid with Individual Differences, Correlated with Diagnostic Marker for Licorice-Induced Pseudoaldosteronism in Humans. Drug Metabolism and Disposition. 52(12). 1407–1416. 3 indexed citations
3.
Kondo, T., Tomoaki Ishida, Ke Ye, et al.. (2022). Suppressive effects of processed aconite root on dexamethasone-induced muscle ring finger protein-1 expression and its active ingredients. Journal of Natural Medicines. 76(3). 594–604. 9 indexed citations
4.
Inoue, Yasumichi, Kan’ichiro Ishiuchi, Michiyo Matsuno, et al.. (2021). Periplocin and cardiac glycosides suppress the unfolded protein response. Scientific Reports. 11(1). 9528–9528. 3 indexed citations
5.
6.
7.
Nakatani, Yoshihiko, Miki Yamauchi, Masato Yoshida, et al.. (2020). Neoline, an active ingredient of the processed aconite root in Goshajinkigan formulation, targets Nav1.7 to ameliorate mechanical hyperalgesia in diabetic mice. Journal of Ethnopharmacology. 259. 112963–112963. 19 indexed citations
8.
Ishiuchi, Kan’ichiro, Osamu Morinaga, Takeshi Ohkita, et al.. (2019). 18β-glycyrrhetyl-3-O-sulfate would be a causative agent of licorice-induced pseudoaldosteronism. Scientific Reports. 9(1). 1587–1587. 27 indexed citations
9.
Yoshino, Tetsuhiro, Kan’ichiro Ishiuchi, Takao Namiki, et al.. (2019). Identification of glycyrrhizin metabolites in humans and of a potential biomarker of liquorice-induced pseudoaldosteronism: a multi-centre cross-sectional study. Archives of Toxicology. 93(11). 3111–3119. 27 indexed citations
10.
Ishiuchi, Kan’ichiro, et al.. (2019). Alpha-pyrone glycosides fromScutellaria salviifoliaBenth. TURKISH JOURNAL OF CHEMISTRY. 43(3). 972–981. 7 indexed citations
11.
Ishiuchi, Kan’ichiro, Xin Xu, Masaaki Minami, et al.. (2018). The immunostimulatory effects and chemical characteristics of heated honey. Journal of Ethnopharmacology. 228. 11–17. 14 indexed citations
12.
Morinaga, Osamu, Kan’ichiro Ishiuchi, Takeshi Ohkita, et al.. (2018). Isolation of a novel glycyrrhizin metabolite as a causal candidate compound for pseudoaldosteronism. Scientific Reports. 8(1). 15568–15568. 27 indexed citations
13.
Ishiuchi, Kan’ichiro, et al.. (2015). Chemical constituents isolated from Juncus effusus induce cytotoxicity in HT22 cells. Journal of Natural Medicines. 69(3). 421–426. 27 indexed citations
14.
Tsunematsu, Yuta, Kan’ichiro Ishiuchi, Kinya Hotta, & Kenji Watanabe. (2013). Yeast-based genome mining, production and mechanistic studies of the biosynthesis of fungal polyketide and peptide natural products. Natural Product Reports. 30(8). 1139–1139. 47 indexed citations
15.
Nakazawa, Takehito, Kan’ichiro Ishiuchi, Alex P. Praseuth, et al.. (2012). Overexpressing Transcriptional Regulator in Aspergillus oryzae Activates a Silent Biosynthetic Pathway to Produce a Novel Polyketide. ChemBioChem. 13(6). 855–861. 34 indexed citations
16.
Ishiuchi, Kan’ichiro, Takehito Nakazawa, Satoru Sugimoto, et al.. (2012). Establishing a New Methodology for Genome Mining and Biosynthesis of Polyketides and Peptides through Yeast Molecular Genetics. ChemBioChem. 13(6). 846–854. 66 indexed citations
17.
Ishiuchi, Kan’ichiro, Takaaki Kubota, Haruaki Ishiyama, et al.. (2010). Lyconadins D and E, and complanadine E, new Lycopodium alkaloids from Lycopodium complanatum. Bioorganic & Medicinal Chemistry. 19(2). 749–753. 54 indexed citations
18.
Ishiuchi, Kan’ichiro, Takaaki Kubota, Shigeki Hayashi, Toshiro Shibata, & Jun’ichi Kobayashi. (2009). Lycopladine H, a novel alkaloid with fused-tetracyclic skeleton from Lycopodium complanatum. Tetrahedron Letters. 50(47). 6534–6536. 29 indexed citations
19.
Ishiuchi, Kan’ichiro, Takaaki Kubota, Hiroshi Morita, & Jun’ichi Kobayashi. (2006). Lycopladine A, a New C16N Alkaloid from Lycopodium complanatum.. ChemInform. 37(35).
20.
Morita, Hiroshi, Kan’ichiro Ishiuchi, Tomohiro Hoshino, et al.. (2005). Complanadine B, Obscurumines A and B, New Alkaloids from Two Species of Lycopodium. ChemInform. 36(27). 1 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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