Toshihiro Imaeda

1.3k total citations
20 papers, 597 citations indexed

About

Toshihiro Imaeda is a scholar working on Molecular Biology, Organic Chemistry and Pharmacology. According to data from OpenAlex, Toshihiro Imaeda has authored 20 papers receiving a total of 597 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 3 papers in Organic Chemistry and 3 papers in Pharmacology. Recurrent topics in Toshihiro Imaeda's work include Receptor Mechanisms and Signaling (4 papers), Biochemical Analysis and Sensing Techniques (3 papers) and Gastroesophageal reflux and treatments (2 papers). Toshihiro Imaeda is often cited by papers focused on Receptor Mechanisms and Signaling (4 papers), Biochemical Analysis and Sensing Techniques (3 papers) and Gastroesophageal reflux and treatments (2 papers). Toshihiro Imaeda collaborates with scholars based in Japan, United States and Canada. Toshihiro Imaeda's co-authors include Kazuyoshi Aso, Rei Okamoto, Jumpei Aida, Katherine Rothamel, J. Fraser Glickman, Yasutomi Asano, Antonio N. Luz, Seth A. Reasoner, Pu Gao and Jessica Vincent and has published in prestigious journals such as Nature Communications, PLoS ONE and Biochemical and Biophysical Research Communications.

In The Last Decade

Toshihiro Imaeda

20 papers receiving 590 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Toshihiro Imaeda Japan 11 334 245 138 78 59 20 597
Kristine Svenson United States 11 330 1.0× 60 0.2× 164 1.2× 61 0.8× 6 0.1× 14 605
Gilles A. Robichaud Canada 18 527 1.6× 174 0.7× 102 0.7× 58 0.7× 3 0.1× 53 927
Hongyan Guo China 12 171 0.5× 143 0.6× 90 0.7× 8 0.1× 32 0.5× 28 510
Zahra Khan South Korea 11 360 1.1× 322 1.3× 70 0.5× 36 0.5× 3 0.1× 17 761
Erli You China 8 155 0.5× 38 0.2× 31 0.2× 79 1.0× 16 0.3× 11 329
Lilia I. Melnik United States 11 306 0.9× 44 0.2× 16 0.1× 42 0.5× 43 0.7× 18 562
Kiyean Nam United States 11 237 0.7× 37 0.2× 115 0.8× 146 1.9× 6 0.1× 24 458
Kou Motani Japan 12 437 1.3× 190 0.8× 99 0.7× 49 0.6× 2 0.0× 17 678
R. B. Lingham United States 8 303 0.9× 35 0.1× 81 0.6× 30 0.4× 11 0.2× 10 469
Ian Parsons Australia 12 478 1.4× 113 0.5× 136 1.0× 27 0.3× 5 0.1× 29 790

Countries citing papers authored by Toshihiro Imaeda

Since Specialization
Citations

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

Fields of papers citing papers by Toshihiro Imaeda

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Toshihiro Imaeda. 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 Toshihiro Imaeda. The network helps show where Toshihiro Imaeda may publish in the future.

Co-authorship network of co-authors of Toshihiro Imaeda

This figure shows the co-authorship network connecting the top 25 collaborators of Toshihiro Imaeda. A scholar is included among the top collaborators of Toshihiro Imaeda 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 Toshihiro Imaeda. Toshihiro Imaeda 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.
Yamashita, Takashi, Toshihiro Imaeda, Hiroyuki Kakei, et al.. (2022). Design and synthesis of 6-methylpyridin-2-one derivatives as novel and potent GluN2A positive allosteric modulators for the treatment of cognitive impairment. Bioorganic & Medicinal Chemistry. 79. 117150–117150. 2 indexed citations
2.
Zhang, Hao, John D. Ginn, Wenhu Zhan, et al.. (2022). Design, Synthesis, and Optimization of Macrocyclic Peptides as Species-Selective Antimalaria Proteasome Inhibitors. Journal of Medicinal Chemistry. 65(13). 9350–9375. 16 indexed citations
3.
Ginn, John D., Xiuju Jiang, Mayako Michino, et al.. (2021). Whole Cell Active Inhibitors of Mycobacterial Lipoamide Dehydrogenase Afford Selectivity over the Human Enzyme through Tight Binding Interactions. ACS Infectious Diseases. 7(2). 435–444. 5 indexed citations
4.
Nogami, Masahiro, Misa Iwatani, Toshihiro Imaeda, et al.. (2020). Identification of a selective DDX3X inhibitor with newly developed quantitative high-throughput RNA helicase assays. Biochemical and Biophysical Research Communications. 523(3). 795–801. 10 indexed citations
5.
Zhan, Wenhu, Hao-Chi Hsu, Trevor Morgan, et al.. (2019). Selective Phenylimidazole-Based Inhibitors of the Mycobacterium tuberculosis Proteasome. Journal of Medicinal Chemistry. 62(20). 9246–9253. 15 indexed citations
6.
Vincent, Jessica, Carolina Adura, Pu Gao, et al.. (2017). Small molecule inhibition of cGAS reduces interferon expression in primary macrophages from autoimmune mice. Nature Communications. 8(1). 750–750. 261 indexed citations
7.
Imaeda, Toshihiro, Koji Ono, Kazuo Nakai, et al.. (2017). Discovery, synthesis, and structure-activity relations of 3,4-dihydro-1H-spiro(naphthalene-2,2′-piperidin)-1-ones as potassium-competitive acid blockers. Bioorganic & Medicinal Chemistry. 25(14). 3719–3735. 10 indexed citations
8.
Nishida, Haruyuki, Yasuyoshi Arikawa, Keizo Hirase, et al.. (2017). Identification of a novel fluoropyrrole derivative as a potassium-competitive acid blocker with long duration of action. Bioorganic & Medicinal Chemistry. 25(13). 3298–3314. 7 indexed citations
9.
Matsumoto, Takahiro, Toshihiro Imaeda, Tōru Kawamura, et al.. (2013). Design, synthesis, and biological evaluation of a series of piperazine ureas as fatty acid amide hydrolase inhibitors. Bioorganic & Medicinal Chemistry. 22(4). 1468–1478. 18 indexed citations
10.
Imaeda, Toshihiro, Toshio Tanaka, Masahiro Kamaura, et al.. (2012). Melanin-Concentrating Hormone Receptor 1 Antagonists. Synthesis and Structure–Activity Relationships of Novel 3-(Aminomethyl)quinolines. Journal of Medicinal Chemistry. 55(5). 2353–2366. 27 indexed citations
11.
Yukitake, Hiroshi, Haruhide Kimura, Hirobumi Suzuki, et al.. (2011). BTZO-15, an ARE-Activator, Ameliorates DSS- and TNBS-Induced Colitis in Rats. PLoS ONE. 6(8). e23256–e23256. 19 indexed citations
12.
Imaeda, Toshihiro, Toshio Tanaka, Jun Terauchi, et al.. (2011). Discovery, synthesis, and structure–activity relationship of 6-aminomethyl-7,8-dihydronaphthalenes as human melanin-concentrating hormone receptor 1 antagonists. Bioorganic & Medicinal Chemistry. 19(18). 5539–5552. 9 indexed citations
13.
Kimura, Haruhide, Yoshimi Sato, Hirobumi Suzuki, et al.. (2010). BTZO-1, a Cardioprotective Agent, Reveals that Macrophage Migration Inhibitory Factor Regulates ARE-Mediated Gene Expression. Chemistry & Biology. 17(12). 1282–1294. 20 indexed citations
14.
15.
Sasaki, Satoshi, Toshihiro Imaeda, Yoji Hayase, et al.. (2002). A new class of potent nonpeptide luteinizing hormone-releasing hormone (LHRH) antagonists: design and synthesis of 2-phenylimidazo[1,2-a]pyrimidin-5-ones. Bioorganic & Medicinal Chemistry Letters. 12(16). 2073–2077. 19 indexed citations
16.
Cho, Nobuo, Masataka Harada, Toshihiro Imaeda, et al.. (1998). Discovery of a Novel, Potent, and Orally Active Nonpeptide Antagonist of the Human Luteinizing Hormone-Releasing Hormone (LHRH) Receptor. Journal of Medicinal Chemistry. 41(22). 4190–4195. 106 indexed citations
17.
Masaki, Yukio, Toshihiro Imaeda, & Makoto Kawai. (1994). Highly Stereoselective Synthesis and Structural Confirmation of a Fungal Metabolite, LL-P880.BETA... Chemical and Pharmaceutical Bulletin. 42(1). 179–181. 3 indexed citations
18.
Masaki, Yukio, Toshihiro Imaeda, Hirohisa Oda, Akichika Itoh, & Motoo Shiro. (1992). Total Synthesis of (+)-Asperlin Starting with (S,S)-Tartaric Acid. Chemistry Letters. 21(7). 1209–1212. 9 indexed citations
19.
Masaki, Yukio, et al.. (1989). Enantiospecific synthesis of optically active natural (+)-conhydrine from (S,S)-tartaric acid. Tetrahedron Letters. 30(46). 6395–6396. 22 indexed citations
20.
Masaki, Yukio, et al.. (1988). Synthesis of (+)-7-ethyl-5-methyl-6,8-dioxabicyclo(3.2.1)oct-3-ene, an optically active form of the house mouse pheromone.. Chemical and Pharmaceutical Bulletin. 36(3). 1241–1244. 5 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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