Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Takanori Matsumaru"'
Autor:
Takanori Matsumaru
Publikováno v:
Trends in Glycoscience and Glycotechnology. 34:E55-E59
Autor:
Takanori Matsumaru, Kasumi Sakuratani, Saeko Yanaka, Koichi Kato, Sho Yamasaki, Yukari Fujimoto
Publikováno v:
European Journal of Organic Chemistry. 2022
Autor:
Akira Katsuyama, Yuma Terasawa, Shin-ichi Yokota, Yukari Fukushima, Fumika Yakushiji, Chie Nakajima, Kazuki Yamamoto, Toyotaka Sato, Takanori Matsumaru, Chisato Sataka, Yasuhiko Suzuki, Satoshi Ichikawa
Publikováno v:
Journal of Medicinal Chemistry. 63:9803-9827
The synthesis and biological evaluation of analogues of uridylpeptide antibiotics were described, and the molecular interaction between the 3'-hydroxy analogue of mureidomycin A (3'-hydroxymureidomycin A) and its target enzyme, phospho-MurNAc-pentape
Autor:
Takanori, Matsumaru, Kodai, Sueyoshi, Kana, Okubo, Shusuke, Fujii, Kasumi, Sakuratani, Ryota, Saito, Kazunari, Ueki, Sho, Yamasaki, Yukari, Fujimoto
Publikováno v:
Bioorganic & Medicinal Chemistry. 75:117045
Mincle, a C-type lectin receptor (CLR), activates the innate immune system by recognizing certain complex lipid compounds. In this study, we designed and synthesized trehalose disteate (TDS) and dibehenate (TDB), containing a polar-functional group i
Publikováno v:
Organic & Biomolecular Chemistry. 18:3659-3663
Ac1PIM1 is a potential biosynthetic intermediate for phosphatidylinositol mannosides (PIMs) from Mycobacterium tuberculosis. We achieved the first synthesis of Ac1PIM1 by utilizing an allyl-type protecting group strategy and regioselective phosphoryl
Autor:
Shinsuke Inuki, Takanori Matsumaru, Ryosuke Yamaguchi, Keisuke Sato, Naoto Zui, Yukari Fujimoto
Publikováno v:
The Journal of Organic Chemistry. 84:12680-12685
FNC-RED exhibits innate immune receptor Toll-like receptor 4 (TLR4)/myeloid differentiation factor-2 (MD2) stimulatory activity. We have developed a divergent synthetic route to FNC-RED derivatives containing various alkyl side chains. Key features o
Autor:
Akihiro Sugawara, Takeshi Yamada, Aoi Kimishima, Takanori Matsumaru, Hirokazu Takada, Toshiaki Sunazuka, Tomoyasu Hirose, Masaki Toda, Toru Kojima
Publikováno v:
Organic letters. 23(5)
Regio- and stereoselective hydrostannylation of alkyl ethynyl ethers generates alkenyl ethers, which are useful building blocks in organic synthesis. This efficient synthetic method, however, is limited. Here, we report not only an efficient method f
Autor:
Katsumi Maenaka, Yusuke Shuchi, Risa Ikeno, Yukari Fujimoto, Toshiki Iwamatsu, Takashi Tadokoro, Takanori Matsumaru, Atsushi Furukawa, Sho Yamasaki
Publikováno v:
Chemical Communications. 55:711-714
Mincle, expressed in activated phagocytes, recognizes the lipid ligand to activate the innate immune system. We have synthesized glycerol derivatives possessing simple alkyl chains or aromatic rings and elucidated their structure-activity relationshi
Autor:
Takanori Matsumaru, Risa Ikeno, Yusuke Shuchi, Toshiki Iwamatsu, Takashi Tadokoro, Sho Yamasaki, Yukari Fujimoto, Atsushi Furukawa, Katsumi Maenaka
Publikováno v:
Chemical Communications. 58:2580-2580
Correction for ‘Synthesis of glycerolipids containing simple linear acyl chains or aromatic rings and evaluation of their Mincle signaling activity’ by Takanori Matsumaru et al., Chem. Commun., 2019, 55, 711–714, DOI: 10.1039/C8CC07322H.
Publikováno v:
CHEMICAL & PHARMACEUTICAL BULLETIN. 66:84-95
A solid-phase synthesis of Park nucleotide as well as lipids I and II analogues, which is applicable to the synthesis of a range of analogues, is described in this work. This technique allows highly functionalized macromolecules to be modularly label