Search Results - "Kurosawa, Sumire"

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  1. 1

    Molecular Basis for Enzymatic Aziridine Formation via Sulfate Elimination by Kurosawa, Sumire, Hasebe, Fumihito, Okamura, Hironori, Yoshida, Ayako, Matsuda, Kenichi, Sone, Yusuke, Tomita, Takeo, Shinada, Tetsuro, Takikawa, Hirosato, Kuzuyama, Tomohisa, Kosono, Saori, Nishiyama, Makoto

    Published in Journal of the American Chemical Society (07-09-2022)
    “…Natural products containing an aziridine ring, such as mitomycin C and azinomycin B, exhibit antitumor activities by alkylating DNA via their aziridine rings;…”
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    Journal Article
  2. 2

    Mechanisms of Sugar Aminotransferase-like Enzymes to Synthesize Stereoisomers of Non-proteinogenic Amino Acids in Natural Product Biosynthesis by Kurosawa, Sumire, Okamura, Hironori, Yoshida, Ayako, Tomita, Takeo, Sone, Yusuke, Hasebe, Fumihito, Shinada, Tetsuro, Takikawa, Hirosato, Kosono, Saori, Nishiyama, Makoto

    Published in ACS chemical biology (17-02-2023)
    “…(2,6)-Diamino-(5,7)-dihydroxyheptanoic acid (DADH), a non-proteinogenic amino acid, is converted to 1-azabicyclo[3.1.0]­hexane ring-containing amino acids that…”
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    Journal Article
  3. 3

    Major intraoperative bleeding and drastic change in circulatory dynamics in a pregnant patient with metastatic pheochromocytoma: a case report by Kurosawa, Sumire, Yamasaki, Hiroyuki, Hasegawa, Wakuya, Mori, Takashi

    Published in JA clinical reports (22-02-2022)
    “…Background Metastatic pheochromocytoma in the spine is a very rare complication during pregnancy. We report anesthesia in a pregnant woman for resection of an…”
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  5. 5

    Structural basis for potent inhibition of d-amino acid oxidase by thiophene carboxylic acids by Kato, Yusuke, Hin, Niyada, Maita, Nobuo, Thomas, Ajit G., Kurosawa, Sumire, Rojas, Camilo, Yorita, Kazuko, Slusher, Barbara S., Fukui, Kiyoshi, Tsukamoto, Takashi

    Published in European journal of medicinal chemistry (05-11-2018)
    “…A series of thiophene-2-carboxylic acids and thiophene-3-carboxylic acids were identified as a new class of DAO inhibitors. Structure-activity relationship…”
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    Journal Article