Masahiro Yonaga

1.2k total citations
35 papers, 922 citations indexed

About

Masahiro Yonaga is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Masahiro Yonaga has authored 35 papers receiving a total of 922 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Organic Chemistry, 9 papers in Molecular Biology and 8 papers in Pharmacology. Recurrent topics in Masahiro Yonaga's work include Asymmetric Synthesis and Catalysis (6 papers), Stress Responses and Cortisol (5 papers) and Neuroscience and Neuropharmacology Research (5 papers). Masahiro Yonaga is often cited by papers focused on Asymmetric Synthesis and Catalysis (6 papers), Stress Responses and Cortisol (5 papers) and Neuroscience and Neuropharmacology Research (5 papers). Masahiro Yonaga collaborates with scholars based in Japan, Russia and United States. Masahiro Yonaga's co-authors include Seiichi Takano, Kunio Ogasawara, Shigeki Hibi, Keigo Tanaka, Norio Murai, Satoshi Nagato, Koichi Ito, Osamu Takenaka, Jennifer M. Finan and Yoshito Kishi and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Journal of Neuroscience.

In The Last Decade

Masahiro Yonaga

34 papers receiving 900 citations

Peers

Masahiro Yonaga
Henner Knust Switzerland
David J. Hallett United Kingdom
Emmanuel Pinard Switzerland
Stephen R. Fletcher United States
T. G. Murali Dhar United States
Curt A. Dvorak United States
Raymond S. Gross United States
Masahiro Yonaga
Citations per year, relative to Masahiro Yonaga Masahiro Yonaga (= 1×) peers Tatsuki Koike

Countries citing papers authored by Masahiro Yonaga

Since Specialization
Citations

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

Fields of papers citing papers by Masahiro Yonaga

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Masahiro Yonaga

This figure shows the co-authorship network connecting the top 25 collaborators of Masahiro Yonaga. A scholar is included among the top collaborators of Masahiro Yonaga 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 Masahiro Yonaga. Masahiro Yonaga 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.
Yonaga, Masahiro, et al.. (2017). Activation of γ-Secretase Trimming Activity by Topological Changes of Transmembrane Domain 1 of Presenilin 1. Journal of Neuroscience. 37(50). 12272–12280. 26 indexed citations
2.
Matsumoto, Yasunobu, Kazuhiro Hibino, Masahiro Yonaga, Hideaki Kakeya, & Yujiro Hayashi. (2016). Enantioselective Total Synthesis of RQN-18690A (18-Deoxyherboxidiene). Organic Letters. 18(14). 3382–3385. 9 indexed citations
3.
Yoshida, Yu, Toshiaki Tanaka, Keiichi Sorimachi, et al.. (2015). Discovery of (1R,2S)-2-{[(2,4-Dimethylpyrimidin-5-yl)oxy]methyl}-2-(3-fluorophenyl)-N-(5-fluoropyridin-2-yl)cyclopropanecarboxamide (E2006): A Potent and Efficacious Oral Orexin Receptor Antagonist. Journal of Medicinal Chemistry. 58(11). 4648–4664. 73 indexed citations
4.
Yoshida, Yu, Yuji Kazuta, Carsten T. Beuckmann, et al.. (2014). Design, synthesis, and structure–activity relationships of a series of novel N-aryl-2-phenylcyclopropanecarboxamide that are potent and orally active orexin receptor antagonists. Bioorganic & Medicinal Chemistry. 22(21). 6071–6088. 20 indexed citations
5.
Ino, Mitsuhiro, et al.. (2012). Design, synthesis and structure–activity relationships of 5-alkylaminolquinolines as a novel series of CRF1 receptor antagonists. Bioorganic & Medicinal Chemistry Letters. 22(14). 4756–4761. 7 indexed citations
6.
Takahashi, Y., Minako Hashizume, Shigeki Hibi, et al.. (2012). Design, Synthesis, and Structure–Activity Relationships of Novel Pyrazolo[5,1-b]thiazole Derivatives as Potent and Orally Active Corticotropin-Releasing Factor 1 Receptor Antagonists. Journal of Medicinal Chemistry. 55(19). 8450–8463. 11 indexed citations
7.
Hashizume, Minako, Kohdoh Shikata, Y. Takahashi, et al.. (2012). Synthesis and structure–activity relationships of 8-substituted-2-aryl-5-alkylaminoquinolines: Potent, orally active corticotropin-releasing factor-1 receptor antagonists. Bioorganic & Medicinal Chemistry. 20(22). 6559–6578. 7 indexed citations
8.
Takahashi, Y., Shigeki Hibi, Yorihisa Hoshino, et al.. (2012). Synthesis and Structure–Activity Relationships of Pyrazolo[1,5-a]pyridine Derivatives: Potent and Orally Active Antagonists of Corticotropin-Releasing Factor 1 Receptor. Journal of Medicinal Chemistry. 55(11). 5255–5269. 32 indexed citations
9.
Hashizume, Minako, et al.. (2012). Design, synthesis, and structure–activity relationships of a series of 2-Ar-8-methyl-5-alkylaminoquinolines as novel CRF1 receptor antagonists. Bioorganic & Medicinal Chemistry Letters. 22(17). 5372–5378. 5 indexed citations
10.
Asai, Naoki, Osamu Takenaka, Hideki Sakurai, et al.. (2007). Synthesis and pharmacological profile of serofendic acids A and B. Bioorganic & Medicinal Chemistry. 15(22). 7098–7107. 14 indexed citations
11.
Yonaga, Masahiro, et al.. (2006). Synthesis and neuroprotective effects of serofendic acid analogues. Bioorganic & Medicinal Chemistry Letters. 16(19). 5080–5083. 10 indexed citations
12.
Nishikawa, Hiroyuki, Toshiaki Kume, Shuji Kaneko, et al.. (2003). Serofendic acid prevents acute glutamate neurotoxicity in cultured cortical neurons. European Journal of Pharmacology. 477(3). 195–203. 25 indexed citations
13.
Suzuki, Yuichi, Noboru Yamamoto, Teiji Kimura, et al.. (2003). Discovery of novel neuronal voltage-Dependent calcium channel blockers based on emopamil left hand as a bioactive template. Bioorganic & Medicinal Chemistry Letters. 13(5). 919–922. 3 indexed citations
14.
Kimura, Teiji, et al.. (2002). Practical Synthesis of Chiral Emopamil Left Hand as a Bioactive Motif. The Journal of Organic Chemistry. 67(17). 6228–6231. 20 indexed citations
15.
Funahashi, Yasuhiro, Naoko Hata Sugi, Taro Semba, et al.. (2002). Sulfonamide derivative, E7820, is a unique angiogenesis inhibitor suppressing an expression of integrin alpha2 subunit on endothelium.. PubMed. 62(21). 6116–23. 94 indexed citations
16.
Yonaga, Masahiro, et al.. (1996). Dopamine D3 agonists disrupt social behavior in rats. Brain Research. 721(1-2). 229–232. 23 indexed citations
17.
Christ, William J., Jennifer M. Finan, Yoshito Kishi, et al.. (1983). ChemInform Abstract: STEREOCHEMISTRY OF PALYTOXIN. PART 4. COMPLETE STRUCTURE. Chemischer Informationsdienst. 14(12). 18 indexed citations
18.
Christ, William J., Jennifer M. Finan, Yoshito Kishi, et al.. (1982). Stereochemistry of palytoxin. Part 4. Complete structure. Journal of the American Chemical Society. 104(25). 7369–7371. 96 indexed citations
19.
Takano, Seiichi, Masahiro Yonaga, & Kunio Ogasawara. (1981). Synthesis of Both Enantiomers of γ-Trityloxymethyl-γ-butyrolactone from a Single Progenitor, (S)-(+)-Glutamic Acid. Synthesis. 1981(4). 265–266. 5 indexed citations
20.
Takano, Seiichi, Masahiro Yonaga, Kenji Chiba, & Kunio Ogasawara. (1980). Enantioselective synthesis of (−)-velbanamine and (+)-isovelbanamine using L-glutamic acid as chiral template. Tetrahedron Letters. 21(38). 3697–3700. 19 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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