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Linkage-Editing of Melibiosamine: Synthesis and Biological Evaluation of CH 2 - and CHF-Linked Analogs.
- 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.
- Subjects :
- Humans
K562 Cells
Antineoplastic Agents pharmacology
Antineoplastic Agents chemistry
Antineoplastic Agents chemical synthesis
Glucosamine chemistry
Disaccharides chemistry
Disaccharides chemical synthesis
Disaccharides pharmacology
Stereoisomerism
Molecular Structure
Galactose chemistry
Drug Screening Assays, Antitumor
Structure-Activity Relationship
Cell Proliferation drug effects
Subjects
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