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Linkage-Editing of Melibiosamine: Synthesis and Biological Evaluation of CH 2 - and CHF-Linked Analogs.

Authors :
Moritsuka N
Kiya N
Moriyama T
Koshino H
Yoritate M
Matoba H
Hirai G
Source :
The Journal of organic chemistry [J Org Chem] 2024 Sep 06; Vol. 89 (17), pp. 11909-11920. Date of Electronic Publication: 2024 Aug 09.
Publication Year :
2024

Abstract

Melibiosamine (Gal-α(1,6)-GlcNH <subscript>2</subscript> ), consisting of galactose and glucosamine linked by an α(1,6)-glycosidic bond, is an artificial disaccharide derivative that selectively inhibits the proliferation of K562 tumor cells relative to HUC-F2 normal cells. In this study, we employed a linkage-editing strategy to synthesize CH <subscript>2</subscript> - and CHF-linked melibiosamine analogs through chemo- and stereoselective hydrogenation of fluorovinyl- C -glycoside. ( R )-CHF-Melibiosamine exhibited more potent antiproliferative activity than O -linked melibiosamine, while ( S )-CHF-melibiosamine was less potent.

Details

Language :
English
ISSN :
1520-6904
Volume :
89
Issue :
17
Database :
MEDLINE
Journal :
The Journal of organic chemistry
Publication Type :
Academic Journal
Accession number :
39119939
Full Text :
https://doi.org/10.1021/acs.joc.4c01143