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- 13C nuclear magnetic resonance spectra of glucobioses, glucotrioses, and glucans. Taichi Usui, Naotaka Yamaoka, Kazuo Matsuda, Katura Tuzimura, Hiroshi Sugiyama, Shuichi Seto
, J. Chem. Soc., Perkin Trans. 1
, 1973
, 2425
- Mechanistic insights into toxicity pathways induced by nanomaterials in Daphnia magna from analysis of the composition of the acquired protein corona. Laura-Jayne A. Ellis, Iseult Lynch
, Environ. Sci.: Nano
, 2020
, 7
, 3343
- Deoxyfluoro-d-trehalose (FDTre) analogues as potential PET probes for imaging mycobacterial infection. Sarah R. Rundell, Zachary L. Wagar, Lisa M. Meints, Claire D. Olson, Mara K. O'Neill, Brent F. Piligian, Anne W. Poston, Robin J. Hood, Peter J. Woodruff, Benjamin M. Swarts
, Org. Biomol. Chem.
, 2016
, 14
, 8598
- The role of chemoenzymatic synthesis in advancing trehalose analogues as tools for combatting bacterial pathogens. Karishma Kalera, Alicyn I. Stothard, Peter J. Woodruff, Benjamin M. Swarts
, Chem. Commun.
, 2020
, 56
, 11528
- Design, synthesis and biological evaluation of sugar-derived esters, α-ketoesters and α-ketoamides as inhibitors for Mycobacterium tuberculosis antigen 85C. Aditya K. Sanki, Julie Boucau, Francis E. Umesiri, Donald R. Ronning, Steven J. Sucheck
, Mol. BioSyst.
, 2009
, 5
, 945
- Thermoresponsive microgels containing trehalose as soft matrices for 3D cell culture. Małgorzata Burek, Sylwia Waśkiewicz, Anna Lalik, Sebastian Student, Tadeusz Bieg, Ilona Wandzik
, Biomater. Sci.
, 2017
, 5
, 234
- Chemical modification of trehalose. Part IX. The monobenzylidene acetal. A. C. Richardson, E. Tarelli
, J. Chem. Soc. C
, 1971
, 3733
- Synthesis of trehalose glycolipids. Santanu Jana, Suvarn S. Kulkarni
, Org. Biomol. Chem.
, 2020
, 18
, 2013
- ortho-Substituted lipidated Brartemicin derivative shows promising Mincle-mediated adjuvant activity. Amy J. Foster, Kristel Kodar, Mattie S. M. Timmer, Bridget L. Stocker
, Org. Biomol. Chem.
, 2020
, 18
, 1095
- Interaction of water with α,α-trehalose in solution: molecular dynamics simulation approach. Maria C. Donnamaria, Eduardo I. Howard, J. Raul Grigera
, J. Chem. Soc., Faraday Trans.
, 1994
, 90
, 2731