Abstract
Glycosylated natural products are reliable platforms for the development of many front-line drugs, yet our understanding of the relationship between attached sugars and biological activity is limited by the availability of convenient glycosylation methods. When a universal chemical glycosylation method that employs reducing sugars and requires no protection or activation is used, the glycorandomization of digitoxin leads to analogs that display significantly enhanced potency and tumor specificity and suggests a divergent mechanistic relationship between cardiac glycoside-induced cytotoxicity and Na+/K+-ATPase inhibition. This report highlights the remarkable advantages of glycorandomization as a powerful tool in glycobiology and drug discovery.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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Antineoplastic Agents / chemical synthesis
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Antineoplastic Agents / chemistry*
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Antineoplastic Agents / pharmacology
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Cardiac Glycosides / chemical synthesis
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Cardiac Glycosides / chemistry*
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Cardiac Glycosides / pharmacology
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Cell Line, Tumor
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Digitoxin / analogs & derivatives
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Digitoxin / chemical synthesis
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Digitoxin / chemistry
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Digitoxin / pharmacology
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Drug Design
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Drug Screening Assays, Antitumor
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Drug Stability
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Enzyme Inhibitors / chemistry
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Enzyme Inhibitors / pharmacology
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Glycosylation
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Humans
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Hydrolysis
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Mice
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Molecular Structure
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Sodium-Potassium-Exchanging ATPase / antagonists & inhibitors
Substances
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Antineoplastic Agents
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Cardiac Glycosides
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Enzyme Inhibitors
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Digitoxin
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Sodium-Potassium-Exchanging ATPase