Kouichi Uoto

1.1k total citations
45 papers, 939 citations indexed

About

Kouichi Uoto is a scholar working on Oncology, Organic Chemistry and Molecular Biology. According to data from OpenAlex, Kouichi Uoto has authored 45 papers receiving a total of 939 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Oncology, 26 papers in Organic Chemistry and 16 papers in Molecular Biology. Recurrent topics in Kouichi Uoto's work include Cancer Treatment and Pharmacology (19 papers), Synthetic Organic Chemistry Methods (13 papers) and Microbial Natural Products and Biosynthesis (8 papers). Kouichi Uoto is often cited by papers focused on Cancer Treatment and Pharmacology (19 papers), Synthetic Organic Chemistry Methods (13 papers) and Microbial Natural Products and Biosynthesis (8 papers). Kouichi Uoto collaborates with scholars based in Japan, Germany and United Kingdom. Kouichi Uoto's co-authors include Tsunehiko Soga, Takao Horiuchi, Hirofumi Terasawa, Satoru Ohsuki, Ikuo Mitsui, Takenori Tomohiro, Jun Chiba, Yasuhide Hirota, Hiroaki Okuno and Akio Ejima and has published in prestigious journals such as Journal of Medicinal Chemistry, The Journal of Organic Chemistry and Bioorganic & Medicinal Chemistry.

In The Last Decade

Kouichi Uoto

45 papers receiving 878 citations

Peers

Kouichi Uoto
María Grazia Ferlin Italy
Ralph P. Robinson United States
Zemei Ge China
Christopher J. Dinsmore United States
Tryfon Zarganes‐Tzitzikas Netherlands
Raed A. Al‐Qawasmeh Jordan
Mariateresa Giustiniano Italy
Pijus K. Mandal United States
Heinz Fretz Switzerland
María Grazia Ferlin Italy
Kouichi Uoto
Citations per year, relative to Kouichi Uoto Kouichi Uoto (= 1×) peers María Grazia Ferlin

Countries citing papers authored by Kouichi Uoto

Since Specialization
Citations

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

Fields of papers citing papers by Kouichi Uoto

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kouichi Uoto

This figure shows the co-authorship network connecting the top 25 collaborators of Kouichi Uoto. A scholar is included among the top collaborators of Kouichi Uoto 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 Kouichi Uoto. Kouichi Uoto 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.
Miyazaki, Kazuo, Kouichi Uoto, Maki Terakawa, et al.. (2020). Design, synthesis, and optimization of a series of 2-azaspiro[3.3]heptane derivatives as orally bioavailable fetal hemoglobin inducers. Bioorganic & Medicinal Chemistry Letters. 30(19). 127425–127425. 4 indexed citations
2.
Miyazaki, Masaki, Kouichi Uoto, Hiroyuki Naito, et al.. (2015). Discovery of DS-5272 as a promising candidate: A potent and orally active p53–MDM2 interaction inhibitor. Bioorganic & Medicinal Chemistry. 23(10). 2360–2367. 31 indexed citations
3.
Yoshikawa, Kenji, Toshiharu Yoshino, Yoshihiro Yokomizo, et al.. (2011). Design, synthesis and SAR of novel ethylenediamine and phenylenediamine derivatives as factor Xa inhibitors. Bioorganic & Medicinal Chemistry Letters. 21(7). 2133–2140. 10 indexed citations
4.
Ishii, Yoshikazu, Eri Watanabe, Kouichi Uoto, et al.. (2010). Inhibition of ergosterol synthesis by novel antifungal compounds targeting C-14 reductase. Medical Mycology. 48(4). 613–621. 28 indexed citations
5.
6.
Horiuchi, Takao, Jun Chiba, Kouichi Uoto, & Tsunehiko Soga. (2008). Discovery of novel thieno[2,3-d]pyrimidin-4-yl hydrazone-based inhibitors of Cyclin D1-CDK4: Synthesis, biological evaluation, and structure–activity relationships. Bioorganic & Medicinal Chemistry Letters. 19(2). 305–308. 85 indexed citations
7.
Naito, Hiroyuki, et al.. (2008). Enantioselective Synthesis of Piperidine Diamine Derivatives as Novel fXa Inhibitors. Heterocycles. 75(7). 1659–1659. 2 indexed citations
8.
Nakamoto, Yumi, et al.. (2007). Design, synthesis, and biological activity of piperidine diamine derivatives as factor Xa inhibitor. Bioorganic & Medicinal Chemistry Letters. 18(2). 782–787. 33 indexed citations
9.
Takeda, Yasuyuki, Kouichi Uoto, Michio Iwahana, et al.. (2004). New highly active taxoids from 9β-dihydrobaccatin-9,10-acetals. Part 5. Bioorganic & Medicinal Chemistry Letters. 14(12). 3209–3215. 2 indexed citations
10.
Takeda, Yasuyuki, Kouichi Uoto, Jun Chiba, et al.. (2003). New highly active taxoids from 9β-Dihydrobaccatin-9,10-acetals. Part 4. Bioorganic & Medicinal Chemistry. 11(20). 4431–4447. 14 indexed citations
11.
Takeda, Yasuyuki, Toshiharu Yoshino, Kouichi Uoto, et al.. (2003). New highly active taxoids from 9β-dihydrobaccatin-9,10-acetals. Part 3. Bioorganic & Medicinal Chemistry Letters. 13(2). 185–190. 17 indexed citations
12.
Ishiyama, Takashi, Shin Iimura, Toshiharu Yoshino, et al.. (2002). New highly active taxoids from 9β-dihydrobaccatin-9,10-acetals. Part 2. Bioorganic & Medicinal Chemistry Letters. 12(20). 2815–2819. 6 indexed citations
13.
Ishiyama, Takashi, Shin Iimura, Satoru Ohsuki, et al.. (2002). New highly active taxoids from 9β-Dihydrobaccatin-9,10-acetals. Bioorganic & Medicinal Chemistry Letters. 12(7). 1083–1086. 21 indexed citations
14.
Nakayama, Kiyoshi, Hirofumi Terasawa, Ikuo Mitsui, et al.. (1998). Synthesis and cytotoxic activity of novel 10-alkylated docetaxel analogs. Bioorganic & Medicinal Chemistry Letters. 8(5). 427–432. 6 indexed citations
15.
Uoto, Kouichi, Teruo Yoshino, Yasuhide Hirota, et al.. (1998). Synthesis and Evaluation of Water-Soluble Non-Prodrug Analogs of Docetaxel Bearing sec-Aminoethyl Group at the C-10 Position.. Chemical and Pharmaceutical Bulletin. 46(5). 770–776. 14 indexed citations
16.
Uoto, Kouichi, Satoru Ohsuki, Takashi Ishiyama, et al.. (1997). Synthesis and Structure-Activity Relationships of Novel 2',2'-Difluoro Analogues of Docetaxel.. Chemical and Pharmaceutical Bulletin. 45(11). 1793–1804. 72 indexed citations
17.
Mitsui, Ikuo, Eiji Kumazawa, Yasuhide Hirota, et al.. (1995). A New Water‐soluble Camptothecin Derivative, DX‐8951f, Exhibits Potent Antitumor Activity against Human Tumors in vitro and in vivo. Japanese Journal of Cancer Research. 86(8). 776–782. 134 indexed citations
18.
Sugimori, Masamichi, Akio Ejima, Satoru Ohsuki, et al.. (1994). Antitumor Agents. VII. Synthesis and Antitumor Activity of Novel Hexacyclic Camptothecin Analogs. Journal of Medicinal Chemistry. 37(19). 3033–3039. 39 indexed citations
19.
20.
Tomohiro, Takenori, Kouichi Uoto, & Hiroaki Okuno. (1990). Synthesis of large macrocyclic tetraaza compounds with a methylene backbone: Cyclo[‐NH‐ (CH2)n‐]4, (n = 6, 7, 8, 9 and 10). The formation of 28‐, 32‐, 36‐, 40‐ and 44‐membered rings. Journal of Heterocyclic Chemistry. 27(5). 1233–1239. 6 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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