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Total Synthesis and Antimicrobial Evaluation of 23-Demethyleushearilide and Extensive Antimicrobial Evaluation of All Synthetic Stereoisomers of (16Z,20E)-Eushearilide and (16E,20E)-Eushearilide.
Tonoi, Takayuki; Inohana, Takehiko; Sato, Teruyuki; Noda, Yuuki; Ikeda, Miyuki; Akutsu, Miku; Murata, Takatsugu; Maekawa, Yutaro; Tanaka, Anna; Seki, Rio; Ohkusu, Misako; Kamei, Katsuhiko; Ishiwada, Naruhiko; Shiina, Isamu.
Afiliación
  • Tonoi T; Department of Applied Chemistry, Faculty of Science, Tokyo University of Science, 1-3 Kagurazaka, Shinjuku-ku, Tokyo 162-8601, Japan. tonoi@rs.tus.ac.jp.
  • Inohana T; Department of Applied Chemistry, Faculty of Science, Tokyo University of Science, 1-3 Kagurazaka, Shinjuku-ku, Tokyo 162-8601, Japan. inohanat@nissanchem.co.jp.
  • Sato T; Department of Applied Chemistry, Faculty of Science, Tokyo University of Science, 1-3 Kagurazaka, Shinjuku-ku, Tokyo 162-8601, Japan. sato-teruyuki@gms.kanto.co.jp.
  • Noda Y; Department of Applied Chemistry, Faculty of Science, Tokyo University of Science, 1-3 Kagurazaka, Shinjuku-ku, Tokyo 162-8601, Japan. 1318598@ed.tus.ac.jp.
  • Ikeda M; Department of Applied Chemistry, Faculty of Science, Tokyo University of Science, 1-3 Kagurazaka, Shinjuku-ku, Tokyo 162-8601, Japan. 1318508@ed.tus.ac.jp.
  • Akutsu M; Department of Applied Chemistry, Faculty of Science, Tokyo University of Science, 1-3 Kagurazaka, Shinjuku-ku, Tokyo 162-8601, Japan. 1319503@ed.tus.ac.jp.
  • Murata T; Department of Applied Chemistry, Faculty of Science, Tokyo University of Science, 1-3 Kagurazaka, Shinjuku-ku, Tokyo 162-8601, Japan. A29215@rs.tus.ac.jp.
  • Maekawa Y; Department of Applied Chemistry, Faculty of Science, Tokyo University of Science, 1-3 Kagurazaka, Shinjuku-ku, Tokyo 162-8601, Japan. 1318617@ed.tus.ac.jp.
  • Tanaka A; Department of Applied Chemistry, Faculty of Science, Tokyo University of Science, 1-3 Kagurazaka, Shinjuku-ku, Tokyo 162-8601, Japan. at.schokolade@gmail.com.
  • Seki R; Department of Infectious Diseases, Medical Mycology Research Center, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba-shi, Chiba 260-8673, Japan. rseki@chiba-u.jp.
  • Ohkusu M; Department of Infectious Diseases, Medical Mycology Research Center, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba-shi, Chiba 260-8673, Japan. misako@office.chiba-u.jp.
  • Kamei K; Department of Infectious Diseases, Medical Mycology Research Center, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba-shi, Chiba 260-8673, Japan. k.kamei@faculty.chiba-u.jp.
  • Ishiwada N; Department of Infectious Diseases, Medical Mycology Research Center, Chiba University, 1-8-1 Inohana, Chuo-ku, Chiba-shi, Chiba 260-8673, Japan. ishiwada@faculty.chiba-u.jp.
  • Shiina I; Department of Applied Chemistry, Faculty of Science, Tokyo University of Science, 1-3 Kagurazaka, Shinjuku-ku, Tokyo 162-8601, Japan. shiina@rs.kagu.tus.ac.jp.
Molecules ; 24(19)2019 Sep 22.
Article en En | MEDLINE | ID: mdl-31546686
ABSTRACT
A novel stereoisomer of eushearilide, 23-demethyleushearilide, was synthesized, and the structure-activity relationships of this compound along with known eushearilide stereoisomers were investigated in order to design novel lead compounds for the treatment of fungal infections. It was discovered that all of these congeners, together with the natural product, exhibited a wide range of antimicrobial activity against not only fungi but also against bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococci (VRE).
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fosforilcolina / Macrólidos Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2019 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Fosforilcolina / Macrólidos Idioma: En Revista: Molecules Asunto de la revista: BIOLOGIA Año: 2019 Tipo del documento: Article