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Journal of the American Chemical Society|June 27, 2002
Asymmetric total synthesis of 11-deoxytetrodotoxin, a naturally occurring congenerToshio Nishikawa, Masanori Asai, Minoru Isobe
Applied and Environmental Microbiology|November 6, 2023
Enhancing the antibacterial function of probiotic Escherichia coli Nissle: when less is moreEmma Bartram, Masanori Asai, Philippe Gabant, et al.
Toxicon : Official Journal of the International Society on Toxinology|October 8, 2003
Biological activity of 8,11-dideoxytetrodotoxin: lethality to mice and the inhibitory activity to cytotoxicity of ouabain and veratridine in mouse neuroblastoma cells, Neuro-2aMari Yotsu-Yamashita, Daisuke Urabe, Masanori Asai, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|January 22, 2004
Stereocontrolled synthesis of 8,11-dideoxytetrodotoxin, an unnatural analogue of puffer fish toxinToshio Nishikawa, Daisuke Urabe, Kazumasa Yoshida, et al.
Organic Letters|August 3, 2002
Stereocontrolled synthesis of 8,11-dideoxytetrodotoxin, unnatural analogue of puffer fish toxinToshio Nishikawa, Daisuke Urabe, Kazumasa Yoshida, et al.
FEMS Microbiology Reviews|March 11, 2023
Galleria mellonella-intracellular bacteria pathogen infection models: the ins and outsMasanori Asai, Yanwen Li, Sandra M Newton, et al.
Bioorganic & Medicinal Chemistry Letters|July 17, 2009
Synthesis and biological evaluation of imidazole derivatives as novel NOP/ORL1 receptor antagonists: exploration and optimization of alternative pyrazole structureYuichi Sugimoto, Kensuke Kobayashi, Masanori Asai, et al.
Frontiers in Microbiology|December 12, 2019
Galleria mellonella: An Infection Model for Screening Compounds Against the Mycobacterium tuberculosis ComplexMasanori Asai, Yanwen Li, Jasmeet Singh Khara, et al.
Frontiers in Cellular and Infection Microbiology|February 26, 2021
Innate Immune Responses of Galleria mellonella to Mycobacterium bovis BCG Challenge Identified Using Proteomic and Molecular ApproachesMasanori Asai, Gerard Sheehan, Yanwen Li, et al.
Bioorganic & Medicinal Chemistry Letters|June 3, 2008
Design, synthesis, and structure-activity relationship study of a novel class of ORL1 receptor antagonists based on N-biarylmethyl spiropiperidineTakashi Yoshizumi, Hiroshi Miyazoe, Hirokatsu Ito, et al.
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