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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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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
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author 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
author_facet 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
author_sort Huang, Yin-Cheng
collection PubMed
description 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.
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spelling pubmed-62682372018-12-20 Synthesis of Amino Core Compounds of Galactosyl Phytosyl Ceramide Analogs for Developing iNKT-Cell Inducers 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 Molecules Article 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. MDPI 2012-03-12 /pmc/articles/PMC6268237/ /pubmed/22410417 http://dx.doi.org/10.3390/molecules17033058 Text en © 2012 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0/ This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
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
Synthesis of Amino Core Compounds of Galactosyl Phytosyl Ceramide Analogs for Developing iNKT-Cell Inducers
title Synthesis of Amino Core Compounds of Galactosyl Phytosyl Ceramide Analogs for Developing iNKT-Cell Inducers
title_full Synthesis of Amino Core Compounds of Galactosyl Phytosyl Ceramide Analogs for Developing iNKT-Cell Inducers
title_fullStr Synthesis of Amino Core Compounds of Galactosyl Phytosyl Ceramide Analogs for Developing iNKT-Cell Inducers
title_full_unstemmed Synthesis of Amino Core Compounds of Galactosyl Phytosyl Ceramide Analogs for Developing iNKT-Cell Inducers
title_short Synthesis of Amino Core Compounds of Galactosyl Phytosyl Ceramide Analogs for Developing iNKT-Cell Inducers
title_sort synthesis of amino core compounds of galactosyl phytosyl ceramide analogs for developing inkt-cell inducers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6268237/
https://www.ncbi.nlm.nih.gov/pubmed/22410417
http://dx.doi.org/10.3390/molecules17033058
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