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Synthesis of Amino Core Compounds of Galactosyl Phytosyl Ceramide Analogs for Developing iNKT-Cell Inducers

1-Aminophytosphingosine and 6-aminogalactosyl phytosphingosine were prepared in 61% and 40% yield libraries with 44 carboxylic acids showed that a 4-butylbenzoic acid-derived product exe, respectively. Glycosylation using benzoyl-protected lipid resulted in better α-selectivity for ceramide analogs,...

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Detalles Bibliográficos
Autores principales: Huang, Yin-Cheng, Chiang, Li-Wu, Chang, Kai-Shiang, Su, Wen-Chin, Lin, Yi-Hsian, Jeng, Kee-Ching, Lin, Kun-I, Liao, Kuo-Yen, Huang, Ho-Lein, Yu, Chung-Shan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268237/
https://www.ncbi.nlm.nih.gov/pubmed/22410417
http://dx.doi.org/10.3390/molecules17033058
Descripción
Sumario:1-Aminophytosphingosine and 6-aminogalactosyl phytosphingosine were prepared in 61% and 40% yield libraries with 44 carboxylic acids showed that a 4-butylbenzoic acid-derived product exe, respectively. Glycosylation using benzoyl-protected lipid resulted in better α-selectivity for ceramide analogs, but the yield was less than that obtained with benzyl moieties. Screening the amide rted less cytotoxicity. These analogs were purified for validation of immunological potencies and the α-GalCer analog but not the sphingosine analog stimulated human iNKT cell population.