Systematic Strategy for the Development of Glycosyltransferase Inhibitors: Diversity-Oriented Synthesis of FUT8 Inhibitors

Author:

Manabe Yoshiyuki12,Fukase Koichi123,Hizume Koki1,Takakura Yohei1,Takamatsu Shinji4,Miyoshi Eiji4,Kamada Yoshihiro5,Hurtado-Guerrero Ramón678

Affiliation:

1. Department of Chemistry, Graduate School of Science, Osaka University

2. Forefront Research Center, Osaka University

3. Center for Advanced Modalities and DDS, Osaka University

4. Department of Molecular Biochemistry and Clinical Investigation, Graduate School of Medicine, Osaka University

5. Department of Advanced Metabolic Hepatology, Graduate School of Medicine, Osaka University

6. Institute of Biocomputation and Physics of Complex Systems (BIFI), University of Zaragoza

7. Fundación ARAID

8. Copenhagen Center for Glycomics, Department of Cellular and Molecular Medicine, University of Copenhagen

Abstract

AbstractGlycans control various biological processes, depending on their structures. Particularly, core fucose, formed by α1,6-fucosyltransferase (FUT8), has a substantial influence on multiple biological processes. In this study, we investigated the development of FUT8 inhibitors with structural elements encompassing both the glycosyl donor (GDP-fucose) and acceptor (N-glycan) of FUT8. To efficiently optimize the structure of FUT8 inhibitors, we employed a strategy involving fragmentation of the target structure, followed by a structure optimization using a diversity-oriented synthesis approach. This study proposes an efficient strategy to accelerate the structural optimization of middle molecules.

Funder

Japan Agency for Medical Research and Development

Core Research for Evolutional Science and Technology

Fusion Oriented Research for Disruptive Science and Technology

Japan Society for the Promotion of Science

Agencia Estatal de Investigación

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry

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