Synthesis of the optically active 4-O-phosphono-d-glucosamine derivatives related to the nonreducing-sugar subunit of bacterial lipid A-Reference-Cited by-同舟云学术

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Synthesis of the optically active 4-O-phosphono-d-glucosamine derivatives related to the nonreducing-sugar subunit of bacterial lipid A

Published:1987-04 Issue:1 Volume:162 Page:127-140
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Kiso Makoto,Tanaka Shinii,Fujita Minoru,Fujishima Yushun,Ogawa Yuji,Ishida Hideharu,Hasegawa Akira

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference23 articles.

1. Synthesis of biologically active, novel monosaccharide analogs of lipid A.

2. Biological activities of chemically synthesized analogues of the nonreducing sugar moiety of lipid A

3. B cell activation and adjuvant activities of chemically synthesized analogues of the nonreducing sugar moiety of lipid A

4. Biological Activities of Chemically Synthesized Partial Structure Analogues of Lipid A1

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2. Modulating LPS Signal Transduction at the LPS Receptor Complex with Synthetic Lipid A Analogues;Advances in Carbohydrate Chemistry and Biochemistry;2014

3. Cell activation by monosaccharide lipid A analogues utilizing Toll-like receptor 4;Immunology;2003-09

4. Synthesis of lipid A type carboxymethyl derivatives with ether chains instead of ester chains and their LPS-antagonistic activities;Carbohydrate Research;2003-01

5. Biophysical Characterization of Triacyl Monosaccharide Lipid A Partial Structures in Relation to Bioactivity;Biophysical Journal;2002-07

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