Session Details

[[A]A305-1pm]16. Natural Products Chemistry, Chemical Biology

Wed. Mar 26, 2025 1:00 PM - 3:30 PM JST
Wed. Mar 26, 2025 4:00 AM - 6:30 AM UTC
[A]A305(A305, Bldg. 1, Area 3 [3F])

[[A]A305-1pm-01]Synthesis of glycopolymer-modified antibodies for cancer immunotherapy using sugar antigens

○Zenya Naraoka1, Sakura Kawahara1, Ryohei Miyagawa2, Yoshiyuki Manabe2, Koichi Fukase2, Tomonari Tanaka1 (1. Kyoto Inst. Tech., 2. Osaka Univ.)

[[A]A305-1pm-02]Synthesis of O-linked glycan core structures using glycoside hydrolases

○Shunsuke Nakada1, Kisuke Tonomura2, Takayuki Ohnuma2, Hisashi Ashida2, Katoh Toshihiko3, Takane Katayama3, Tomonari Tanaka1 (1. Kyoto Institute of Technology, 2. Kindai Univ., 3. Kyoto Univ.)

[[A]A305-1pm-03]Creation of a New Macrolide Antibiotic against Non-tuberculous Mycobacterium by Late-stage Boron-mediated Aglycon Delivery

○Yuka Isozaki1, Takumi Makikawa1, Kosuke Kimura1, Daiki Nishihara2, Maho Fujino2, Yoshikazu Tanaka2, Chigusa Hayashi3, Yoshimasa Ishizaki3, Masayuki Igarashi3, Takeshi Yokoyama2, Kazunobu Toshima1, Daisuke Takahashi1 (1. Keio University, 2. Tohoku University, 3. Institute of Microbial Chemistry)

[[A]A305-1pm-04]Elucidation of novel glycan functions that promote an α-helix formation of peptides

○Intan Hawina Anjari1, Kohtaro Hirao1,2, Yuta Maki1,2, Ryo Okamoto1,2, Yasuhiro Kajihara1,2 (1. Grad. Sch. Sci. Osaka Univ., 2. FRC, Grad. Sch. Sci. Osaka Univ.)

Break

[[A]A305-1pm-05]Synthesis and properties of α-helical peptides doubly-crosslinked with isophthalic acid-based crosslinking agents

○Tetsuya Yasukagawa1, Junuya Chiba1, Yuki Ohishi1, Satoru Yokoyama1, Zhou Yue1, Masahiko Inouye1 (1. The Univ. of Toyama)

[[A]A305-1pm-06]Development of Growth Inhibitor for Mushroom Based on Coprinoferrin

○Tomohiro Tsutsumi1, Haruka Suda1, Chika Ando2, Yuta Tsunematsu2, Ichiro Hayakawa1 (1. Graduate School of Integrated Basic Sciences, Nihon University, 2. Graduate School of Bioagricultural Sciences, Nagoya University)

[[A]A305-1pm-07]Development of thiazole-containing cyclic peptide ligands by an mRNA-display-coupled post-translational chemoenzymatic modifications

○Akihiro Saito1, Hiroaki Suga2, Yuki Goto1 (1. Kyoto University, 2. The University of Tokyo)