KAMAUCHI Hitoshi

写真a

Affiliation

Faculty of Pharmaceutical Sciences Department of Pharmaceutical Technochemistry

Title

Assistant Professor

External Link

Degree 【 display / non-display

  • 博士 (薬科学) ( 2018.03   明治薬科大学 )

Research Interests 【 display / non-display

  • Natural product science

Research Areas 【 display / non-display

  • Life Science / Environmental and natural pharmaceutical resources

  • Life Science / Pharmaceutical chemistry and drug development sciences

From School 【 display / non-display

  • Meiji Pharmaceutical University   Faculty of Pharmaceutical Science   Graduated

    2006.04 - 2010.03

      More details

    Country:Japan

From Graduate School 【 display / non-display

  • Meiji Pharmaceutical University   Graduate School, Division of Pharmaceutical Sciences   Doctor's Course   Completed

    2015.04 - 2018.03

      More details

    Country:Japan

  • Meiji Pharmaceutical University   Graduate School, Division of Pharmaceutical Sciences   Master's Course   Completed

    2013.04 - 2015.03

      More details

    Country:Japan

Employment Record in Research 【 display / non-display

  • Josai University   Faculty of Pharmaceutical Sciences   Department of Pharmaceutical Technochemistry   Assistant Professor

    2022.04

  • Josai University   Faculty of Pharmaceutical Sciences   Department of Pharmaceutical Technochemistry   Research Assistant

    2018.04 - 2022.03

External Career 【 display / non-display

  • Meiji Pharmaceutical University   Researcher

    2011.04 - 2013.03

      More details

    Country:Japan

Professional Memberships 【 display / non-display

  • 有機合成化学協会

    2018.11

  • 日本薬学会

    2013.04

  • 日本生薬学会

    2013.04

 

Papers 【 display / non-display

  • Synthesis and Biological Evaluation of 2-Azolylmethylene-3-(2H)-benzofuranone Derivatives as Potent Monoamine Oxidases Inhibitors Reviewed

    Koichi Takao, Yuka Kubota, Kota Kurosaki, Hitoshi Kamauchi, Yoshihiro Uesawa, Yoshiaki Sugita

    Chemical and Pharmaceutical Bulletin   72 ( 1 )   109 - 120   2024.01

     More details

    Publishing type:Research paper (scientific journal)   Publisher:Pharmaceutical Society of Japan  

    DOI: 10.1248/cpb.c23-00763

    researchmap

  • A Tricyclic Aromatic Polyketide Isolated from the Marine-Derived Fungus Curvularia aeria Reviewed

    Hitoshi Kamauchi, Mayu Tanaka, Mitsuaki Suzuki, Miho Furukawa, Atsushi Ikeda, Chihiro Sasho, Yuka Kiba, Masashi Kitamura, Koichi Takao, Yoshiaki Sugita

    Chemical and Pharmaceutical Bulletin   72 ( 1 )   98 - 101   2024.01

     More details

    Authorship:Lead author, Corresponding author   Publishing type:Research paper (scientific journal)   Publisher:Pharmaceutical Society of Japan  

    DOI: 10.1248/cpb.c23-00723

    researchmap

  • Synthesis of 2,8-Dioxabicyclo[3.3.1]nonane Derivatives and Their Neuroprotective Activities Reviewed

    Hitoshi Kamauchi, Akifumi Takanashi, Mitsuaki Suzuki, Kouki Izumi, Koichi Takao, Yoshiaki Sugita

    Chemical and Pharmaceutical Bulletin   72 ( 1 )   56 - 60   2024.01

     More details

    Authorship:Lead author, Corresponding author   Publishing type:Research paper (scientific journal)   Publisher:Pharmaceutical Society of Japan  

    DOI: 10.1248/cpb.c23-00693

    researchmap

  • Inhibition of furin-like enzymatic activities and SARS-CoV-2 infection by osthole and phenolic compounds with aryl side chains. International journal

    Yuka Kiba, Takashi Tanikawa, Tsuyoshi Hayashi, Hitoshi Kamauchi, Taishi Seki, Ryuichiro Suzuki, Masashi Kitamura

    Biomedicine & pharmacotherapy   169   115940 - 115940   2023.11

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), spread as a pandemic and caused damage to people's lives and countries' economies. The spike (S) protein of SARS-CoV-2 contains a cleavage motif, Arg-X-X-Arg, for furin and furin-like enzymes at the boundary of the S1/S2 subunits. Given that cleavage plays a crucial role in S protein activation and viral entry, the cleavage motif was selected as the target. Our previous fluorogenic substrate study showed that osthole, a coumarin compound, inhibits furin-like enzyme activity. In this study, we examined the potential activities of 15 compounds with a structure-activity relationship with osthole, and evaluated their protective ability against SARS-CoV-2 infection. Of the 15 compounds tested, compounds C1 and C2 exhibited the inhibitory effects of osthole against furin-like enzymatic activity; however, little or no inhibitory effects against furin activity were observed. We further examined the inhibition of SARS-CoV-2 activity by compounds C1 and C2 using a Vero E6 cell line that expresses the transmembrane protease serine 2 (TMPRSS2). Compounds C1, C2, and osthole effectively inhibited SARS-CoV-2 infection. Therefore, osthole and its derivatives can potentially be used as therapeutic agents against SARS-CoV-2.

    DOI: 10.1016/j.biopha.2023.115940

    PubMed

    researchmap

  • Total Synthesis and Monoamine Oxidase Inhibitory Activities of (±)-Entonalactam A and Its Derivatives Reviewed

    Hitoshi Kamauchi, Momoka Hirata, Koichi Takao, Yoshiaki Sugita

    ACS Omega   7 ( 45 )   41804 - 41814   2022.11

     More details

    Authorship:Lead author, Corresponding author   Language:English   Publishing type:Research paper (scientific journal)   Publisher:American Chemical Society (ACS)  

    DOI: 10.1021/acsomega.2c06260

    researchmap

display all >>

Misc 【 display / non-display

  • Discovery of Medicinal Seeds from Chemically Engineered Extracts Invited Reviewed

    Journal of Synthetic Organic Chemistry, Japan   77 ( 9 )   895 - 903   2019.09

     More details

    Language:Japanese   Publishing type:Article, review, commentary, editorial, etc. (scientific journal)  

    researchmap

  • Discovery of Medicinal Seeds from Chemically Engineered Extracts Invited Reviewed

    Journal of Synthetic Organic Chemistry, Japan   77 ( 9 )   895 - 903   2019.09

     More details

    Authorship:Lead author   Language:Japanese   Publishing type:Article, review, commentary, editorial, etc. (scientific journal)  

  • エンドファイト; 特殊環境が生み出す可能性 Invited Reviewed

    鎌内 等

    ファルマシア   49 ( 4 )   333   2013.04

     More details

    Authorship:Lead author   Language:Japanese   Publishing type:Article, review, commentary, editorial, etc. (scientific journal)   Publisher:公益社団法人日本薬学会  

  • エンドファイト; 特殊環境が生み出す可能性 Invited Reviewed

    鎌内 等

    ファルマシア   49 ( 4 )   333 - 333   2013.04

     More details

    Language:Japanese   Publishing type:Article, review, commentary, editorial, etc. (scientific journal)   Publisher:公益社団法人日本薬学会  

    DOI: 10.14894/faruawpsj.49.4_333

    CiNii Articles

    CiNii Books

    researchmap

Presentations 【 display / non-display

  • クロサイワイタケ科キノコ由来イソインドリノン化合物の合成

    鎌内 等, 杉田 義昭

    第65回天然有機化合物討論会  2023.09 

     More details

    Event date: 2023.09

    researchmap

  • 菌糸-バイオフィルム形成阻害をターゲットとした真菌由来天然物の誘導体合成

    鎌内 等, 木村 由, 牛渡 美琴, 關 大志, 鈴木 光明, 平田 桃香, 高尾 浩一, 杉田 義昭

    第63回天然有機化合物討論会  2021.09 

     More details

    Event date: 2021.09

    researchmap

  • 芳香族-テルペノイド天然物の誘導体合成と神経保護作用の評価

    鎌内 等, 小田 拓未, 堀内 加奈世, 高尾 浩一, 杉田 義昭

    第61回天然有機化合物討論会  2019.09 

     More details

    Event date: 2019.09

    researchmap

Awards 【 display / non-display

  • 長井記念若手薬学研究者賞

    2023.03   日本薬学会  

    鎌内 等

     More details

    Award type:Award from Japanese society, conference, symposium, etc.  Country:Japan

  • 長井記念若手薬学研究者賞

    2023.03   日本薬学会  

    鎌内 等

     More details

    Award type:Award from Japanese society, conference, symposium, etc.  Country:Japan

    researchmap

  • 平成28年度長井記念薬学研究奨励支援

    2016   日本薬学会  

    鎌内 等

     More details

    Award type:Award from Japanese society, conference, symposium, etc.  Country:Japan

  • 平成28年度長井記念薬学研究奨励支援

    2016   日本薬学会  

    鎌内 等

     More details

    Award type:Award from Japanese society, conference, symposium, etc.  Country:Japan

    researchmap

Scientific Research Funds Acquisition Results 【 display / non-display

  • 天然由来化合物を基盤とした菌糸形成阻害による「予防的」抗真菌薬の開発

    Grant number:20K16029  2020.04 - 2023.03

    科学研究費助成事業  若手研究

    鎌内等

      More details

    Authorship:Principal investigator  Grant type:Competitive

    researchmap

  • 天然由来化合物を基盤とした菌糸形成阻害による「予防的」抗真菌薬の開発

    2020.01 - 2023.03

    科学研究費補助金  若手研究

    鎌内等