rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
22
|
pubmed:dateCreated |
2007-10-25
|
pubmed:abstractText |
Two new C-1 epimeric hydroxymethyl castanospermine congeners 2a and 2b, synthesized by stereocontrolled intramolecular double reductive amination of D-glucose derived beta-keto ester as a key step, showed impressive immuno-potentiating property. The bioactivity was mediated through up-regulation of T(H1)/T(H2) cytokine ratio. The finding suggested that immunmodulatory activity of polyhydroxylated indolizidine alkaloids can be tuned by minor structural/stereochemical alterations.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
|
pubmed:issn |
0022-2623
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:day |
1
|
pubmed:volume |
50
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
5519-23
|
pubmed:meshHeading |
pubmed-meshheading:17918922-Adjuvants, Immunologic,
pubmed-meshheading:17918922-Animals,
pubmed-meshheading:17918922-Cell Proliferation,
pubmed-meshheading:17918922-Concanavalin A,
pubmed-meshheading:17918922-Cytokines,
pubmed-meshheading:17918922-Drug Synergism,
pubmed-meshheading:17918922-Indolizines,
pubmed-meshheading:17918922-Mice,
pubmed-meshheading:17918922-Spleen,
pubmed-meshheading:17918922-Stereoisomerism,
pubmed-meshheading:17918922-Th1 Cells,
pubmed-meshheading:17918922-Th2 Cells
|
pubmed:year |
2007
|
pubmed:articleTitle |
Synthesis of 1-deoxy-1-hydroxymethyl- and 1-deoxy-1-epi-hydroxymethyl castanospermine as new potential immunomodulating agents.
|
pubmed:affiliation |
Garware Research Centre, Department of Chemistry, University of Pune, Pune-411 007, India.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|