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Satoshi Shuto

Satoshi Shuto

Hokkaido University
Japan

D-Index & Metrics

Chemistry

D-Index
55
Citations
9223
World Ranking
12306
National Ranking
923

Satoshi Shuto publication distribution in Chemistry in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Chemistry in 2026. The highlighted bar marks where Satoshi Shuto sits on this spectrum.

61–80 publications: 66 scientists 81–100 publications: 302 scientists 101–120 publications: 623 scientists 121–140 publications: 918 scientists 141–160 publications: 1,218 scientists 161–180 publications: 1,350 scientists 181–200 publications: 1,344 scientists 201–220 publications: 1,281 scientists 221–240 publications: 1,216 scientists 241–260 publications: 1,100 scientists 261–280 publications: 979 scientists 281–300 publications: 939 scientists 301–320 publications: 764 scientists 321–340 publications: 643 scientists 341–360 publications: 628 scientists 361–380 publications: 522 scientists 381–400 publications: 459 scientists 401–420 publications: 397 scientists 421–440 publications: 327 scientists 441–460 publications: 270 scientists 461–480 publications: 265 scientists 481–500 publications: 252 scientists 501–520 publications: 201 scientists 521–540 publications: 185 scientists 541–560 publications: 148 scientists 561–580 publications: 148 scientists 581–600 publications: 132 scientists 601–620 publications: 114 scientists 621–640 publications: 104 scientists 641–660 publications: 91 scientists 661–680 publications: 92 scientists 681–700 publications: 73 scientists 701–720 publications: 57 scientists 721–740 publications: 54 scientists 741–760 publications: 67 scientists 761–780 publications: 45 scientists 781–800 publications: 46 scientists 801–820 publications: 39 scientists 821–840 publications: 32 scientists 841–860 publications: 36 scientists 861–880 publications: 29 scientists 881–900 publications: 26 scientists 901–920 publications: 24 scientists 921–940 publications: 14 scientists 941–960 publications: 23 scientists 961–980 publications: 28 scientists 981–1,000 publications: 15 scientists 1,001–1,020 publications: 29 scientists 1,021–1,040 publications: 12 scientists 1,041–1,060 publications: 19 scientists 1,061–1,080 publications: 12 scientists 1,081–1,100 publications: 6 scientists 1,101–1,120 publications: 8 scientists 1,121–1,140 publications: 12 scientists 1,141–1,160 publications: 5 scientists 1,161–1,180 publications: 6 scientists 1,181–1,200 publications: 14 scientists 1,201–1,220 publications: 7 scientists 1,221–1,240 publications: 2 scientists 1,241–1,260 publications: 6 scientists 1,261–1,280 publications: 4 scientists 1,281–1,294 publications: 6 scientists 1,295+ publications: 100 scientists
61 publications 1,295+

This scientist: 402 publications — 80th percentile

80% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 1,295 publications or more.

Satoshi Shuto D-index placement in Chemistry in 2026

The chart shows the D-index (discipline H-index) distribution of Chemistry scientists ranked by Research.com in 2026. The highlighted bar marks where Satoshi Shuto sits on this spectrum.

40–41 D-Index: 289 scientists 42–43 D-Index: 612 scientists 44–45 D-Index: 808 scientists 46–47 D-Index: 776 scientists 48–49 D-Index: 835 scientists 50–51 D-Index: 861 scientists 52–53 D-Index: 872 scientists 54–55 D-Index: 933 scientists 56–57 D-Index: 1,051 scientists 58–59 D-Index: 930 scientists 60–61 D-Index: 882 scientists 62–63 D-Index: 834 scientists 64–65 D-Index: 731 scientists 66–67 D-Index: 775 scientists 68–69 D-Index: 683 scientists 70–71 D-Index: 646 scientists 72–73 D-Index: 561 scientists 74–75 D-Index: 501 scientists 76–77 D-Index: 437 scientists 78–79 D-Index: 388 scientists 80–81 D-Index: 354 scientists 82–83 D-Index: 292 scientists 84–85 D-Index: 275 scientists 86–87 D-Index: 254 scientists 88–89 D-Index: 235 scientists 90–91 D-Index: 185 scientists 92–93 D-Index: 192 scientists 94–95 D-Index: 155 scientists 96–97 D-Index: 163 scientists 98–99 D-Index: 125 scientists 100–101 D-Index: 105 scientists 102–103 D-Index: 105 scientists 104–105 D-Index: 112 scientists 106–107 D-Index: 88 scientists 108–109 D-Index: 68 scientists 110–111 D-Index: 69 scientists 112–113 D-Index: 65 scientists 114–115 D-Index: 79 scientists 116–117 D-Index: 61 scientists 118–119 D-Index: 44 scientists 120–121 D-Index: 37 scientists 122–123 D-Index: 40 scientists 124–125 D-Index: 33 scientists 126–127 D-Index: 26 scientists 128–129 D-Index: 34 scientists 130–131 D-Index: 35 scientists 132–133 D-Index: 25 scientists 134–135 D-Index: 27 scientists 136–137 D-Index: 17 scientists 138–139 D-Index: 16 scientists 140–141 D-Index: 20 scientists 142–143 D-Index: 20 scientists 144–145 D-Index: 15 scientists 146–147 D-Index: 9 scientists 148–149 D-Index: 9 scientists 150–151 D-Index: 16 scientists 152–153 D-Index: 11 scientists 154–155 D-Index: 9 scientists 156–157 D-Index: 3 scientists 158 D-Index: 3 scientists 159+ D-Index: 98 scientists
40 D-Index 159+

This scientist: 55 D-Index — 33rd percentile

33% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 159 D-Index or more.

Overview

Satoshi Shuto is affiliated with Hokkaido University in Japan. Their research spans several fields, primarily focusing on biochemistry, genetics, and molecular biology as well as medicine.

The main fields of study for Shuto include:

  • Biochemistry, Genetics and Molecular Biology
  • Medicine

Their subfields of expertise cover:

  • Molecular Biology
  • Organic Chemistry
  • Immunology
  • Physiology
  • Cellular and Molecular Neuroscience

Shuto's research topics include:

  • Chemical Synthesis and Analysis
  • Neuroscience and Neuropharmacology Research
  • Fatty Acid Research and Health
  • Stress Responses and Cortisol
  • Eicosanoids and Hypertension Pharmacology
  • Peroxisome Proliferator-Activated Receptors
  • RNA and protein synthesis mechanisms

Among the recent papers authored or co-authored by Satoshi Shuto are:

  • Delivering mRNA to Secondary Lymphoid Tissues by Phosphatidylserine-Loaded Lipid Nanoparticles (2022), published in Advanced Healthcare Materials
  • Discovery of [1,2,4]Triazolo[1,5-a]pyridine Derivatives as Potent and Orally Bioavailable RORγt Inverse Agonists (2020), published in ACS Medicinal Chemistry Letters
  • Design and Synthesis of Benzene Congeners of Resolvin E2, a Proresolving Lipid Mediator, as Its Stable Equivalents (2020), published in ACS Medicinal Chemistry Letters
  • Synthesis of Resolvin E3, a Proresolving Lipid Mediator, and Its Deoxy Derivatives: Identification of 18-Deoxy-resolvin E3 as a Potent Anti-Inflammatory Agent (2020), published in The Journal of Organic Chemistry
  • Resolvin E1 Attenuates Chronic Pain-Induced Depression-Like Behavior in Mice: Possible Involvement of Chemerin Receptor ChemR23 (2021), published in Biological and Pharmaceutical Bulletin

Frequent co-authors working with Shuto include:

  • Mizuki Watanabe
  • Hayato Fukuda
  • Koichi Fujiwara
  • Kohei Ishimura
  • Satoshi Deyama

Prominent venues where Shuto's work has appeared encompass:

  • ACS Medicinal Chemistry Letters
  • The Journal of Organic Chemistry
  • Bioorganic & Medicinal Chemistry Letters
  • Organic Letters
  • Proceedings for Annual Meeting of The Japanese Pharmacological Society

Best Publications

  • Rolling Circle Translation of Circular RNA in Living Human Cells

    Naoko Abe;Ken Matsumoto;Mizuki Nishihara;Yukiko Nakano

  • Highly α- and β-Selective Radical C-Glycosylation Reactions Using a Controlling Anomeric Effect Based on the Conformational Restriction Strategy. A Study on the Conformation−Anomeric Effect− Stereoselectivity Relationship in Anomeric Radical Reactions

    Hiroshi Abe;Satoshi Shuto;Akira Matsuda

  • Nucleosides and nucleotides. 185. Synthesis and biological activities of 4'alpha-C-branched-chain sugar pyrimidine nucleosides.

    Makoto Nomura;Satoshi Shuto;Motohiro Tanaka;Takuma Sasaki

  • A facile one-step synthesis of 5'-phosphatidylnucleosides by an enzymatic two-phase reaction

    Satoshi Shuto;Shigeru Ueda;Shigeyuki Imamura;Kiyofumi Fukukawa

  • Conformational Restriction by Repulsion between Adjacent Substituents on a Cyclopropane Ring: Design and Enantioselective Synthesis of 1-Phenyl-2-(1-aminoalkyl)-N,N-diethylcyclopropanecarboxamides as Potent NMDA Receptor Antagonists

    Satoshi Shuto;Shizuka Ono;Yukako Hase;Noriko Kamiyama

  • Synthesis and characterization of a series of highly fluorogenic substrates for glutathione transferases, a general strategy.

    Jie Zhang;Aya Shibata;Mika Ito;Satoshi Shuto

  • Nucleosides and nucleotides. 183. Synthesis of 4′ α-branched thymidines as a new type of antiviral agent

    Isamu Sugimoto;Satoshi Shuto;Shuichi Mori;Shiro Shigeta

  • Development of versatile cis- and trans-dicarbon-substituted chiral cyclopropane units: synthesis of (1S,2R)- and (1R,2R)-2-aminomethyl-1-(1H-imidazol-4-yl)cyclopropanes and their enantiomers as conformationally restricted analogues of histamine.

    Yuji Kazuta;and Akira Matsuda;Satoshi Shuto

  • The First Synthesis of Herbicidin B. Stereoselective Construction of the Tricyclic Undecose Moiety by a Conformational Restriction Strategy Using Steric Repulsion between Adjacent Bulky Silyl Protecting Groups on a Pyranose Ring

    Satoshi Ichikawa;and Satoshi Shuto;Akira Matsuda

  • A facile enzymatic synthesis of 5'-(3-sn-phosphatidyl)nucleosides and their antileukemic activities.

    Satoshi Shuto;Hiromichi Itoh;Shigeru Ueda;Shigeyuki Imamura

  • Sulfur Modification of Au via Treatment with Piranha Solution Provides Low-Pd Releasing and Recyclable Pd Material, SAPd

    Naoyuki Hoshiya;Masahiko Shimoda;Hideki Yoshikawa;Yoshiyuki Yamashita

  • Cyclopropane-based conformational restriction of histamine. (1S,2S)-2-(2-aminoethyl)-1-(1H-imidazol-4-yl)cyclopropane, a highly selective agonist for the histamine H3 receptor, having a cis-cyclopropane structure.

    Yuji Kazuta;Kazufumi Hirano;Kentaro Natsume;Shizuo Yamada

  • Palladium-Catalyzed Arylation of Cyclopropanes via Directing Group-Mediated C(sp3)–H Bond Activation To Construct Quaternary Carbon Centers: Synthesis of cis- and trans-1,1,2-Trisubstituted Chiral Cyclopropanes

    Naoyuki Hoshiya;Takaaki Kobayashi;Mitsuhiro Arisawa;Satoshi Shuto

  • New neplanocin analogues. 1. Synthesis of 6'-modified neplanocin A derivatives as broad-spectrum antiviral agents.

    Satoshi Shuto;Takumi Obara;Minoru Toriya;Mitsuaki Hosoya

  • Nucleosides and nucleotides. 175. Structural requirements of the sugar moiety for the antitumor activities of new nucleoside antimetabolites, 1-(3-C-ethynyl-beta-D-ribo-pentofuranosyl)cytosine and -uracil1

    Hideshi Hattori;Eisuke Nozawa;Tomoharu Iino;Yuichi Yoshimura

  • (.+-.)-(Z)-2-(Aminomethyl)-1-phenylcyclopropanecarboxamide Derivatives as a New Prototype of NMDA Receptor Antagonists

    Satoshi Shuto;Hironao Takada;Daisuke Mochizuki;Ryuichi Tsujita

  • Total Synthesis of Cyclic ADP-carbocyclic-ribose, a Stable Mimic of Ca2+-Mobilizing Second Messenger Cyclic ADP-Ribose1

    Satoshi Shuto;Masayoshi Fukuoka;Andrzej Manikowsky;Yoshihito Ueno

  • Construction of a cis-Cyclopropane via Reductive Radical Decarboxylation. Enantioselective Synthesis of cis- and trans-1-Arylpiperazyl-2-phenylcyclopropanes Designed as Antidopaminergic Agents

    Kazuya Yamaguchi;Yuji Kazuta;Hiroshi Abe;and Akira Matsuda

  • Anti-neovascular therapy by liposomal DPP-CNDAC targeted to angiogenic vessels.

    Tomohiro Asai;Kosuke Shimizu;Masami Kondo;Koichi Kuromi

  • Nucleosides and nucleotides. 132. Synthesis and biological evaluations of ring-expanded oxetanocin analogues: Purine and pyrimidine analogues of 1,4-anhydro-2-deoxy-d-arabitol and 1,4-anhydro-2-deoxy-3-hydroxymethyl-d-arabitol

    Akio Kakefuda;Satoshi Shuto;Takemitsu Nagahata;Jun-ichi Seki

  • 1,2,3-Triazole-containing uracil derivatives with excellent pharmacokinetics as a novel class of potent human deoxyuridine triphosphatase inhibitors.

    Hitoshi Miyakoshi;Seiji Miyahara;Tatsushi Yokogawa;Kanji Endoh

Frequent Co-Authors

Akira Matsuda
Akira Matsuda Juntendo University
Hiroshi Abe
Hiroshi Abe Nagoya University
Barry V. L. Potter
Barry V. L. Potter University of Oxford
Yoshihiro Ito
Yoshihiro Ito RIKEN
Haruhiro Higashida
Haruhiro Higashida Kanazawa University
Shizuo Yamada
Shizuo Yamada University of Shizuoka
Shiro Shigeta
Shiro Shigeta Fukushima Medical University
Masanori Baba
Masanori Baba Kagoshima University
Tadashi Matsuda
Tadashi Matsuda Hokkaido University
Bengt Mannervik
Bengt Mannervik Stockholm University

External Links

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