Results 111 to 120 of about 4,713 (170)
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Structure-Activity Relationship of .alpha.-Galactosylceramides against B16-Bearing Mice
Journal of Medicinal Chemistry, 1995Kazuhiro Motoki +2 more
exaly +2 more sources
Agelasphins, novel α-galactosylceramides from the marine sponge Agelas mauritianus
Tetrahedron Letters, 1993Tatsuo Higa, Yasuhiko Koezuka
exaly +2 more sources
Two novel galactosylceramides from Marphysa sanguinea
Tetrahedron Letters, 1992Kazumoto Miyahara, Naoki Noda
exaly +2 more sources
An Efficient and Concise Synthesis of α-Galactosylceramide
Synlett, 2020AbstractA concise and stereoselective synthesis of α-galactosylceramide (α-GalCer) is described. The key features of the synthetic strategy are the use of a phytosphingosine in which the amine is masked as a tetrachlorophthalimide and the diol as an isopropylidene acetal, and the galactosyl donor is protected as a 4,6-benzylidene to improve the α ...
Daniela Imperio +3 more
openaire +4 more sources
Carbohydrate Research, 2019
Herein, an efficient synthesis of BODIPY-α-Galactosylceramide 3, which can be used to study the cellular uptake of the potent immunostimulatory parent compound α-Galactosylceramide, is reported. Key in our synthetic strategy is the six-step synthesis of the core BODIPY scaffold (64% yield overall) and its quantitative conversion to an N ...
Cheng, Janice M.H. +5 more
openaire +3 more sources
Herein, an efficient synthesis of BODIPY-α-Galactosylceramide 3, which can be used to study the cellular uptake of the potent immunostimulatory parent compound α-Galactosylceramide, is reported. Key in our synthetic strategy is the six-step synthesis of the core BODIPY scaffold (64% yield overall) and its quantitative conversion to an N ...
Cheng, Janice M.H. +5 more
openaire +3 more sources