| Literature DB >> 26487911 |
Jianjun Zhang1, Larissa V Ponomareva1, Nitin S Nandurkar1, Yaxia Yuan1, Lei Fang1, Chang-Guo Zhan1, Jon S Thorson1.
Abstract
The synthesis of a set of digitoxigenin neogluco/xylosides and corresponding study of their anticancer SAR revealed sugar amine regiochemistry has a dramatic effect upon activity. Specifically, this study noted sugar 3-amino followed by 4-amino-substitution to be most advantageous where the solvent accessibility of the appended amine within neoglycoside-Na(+),K(+)-ATPase docked models correlated with increased anticancer potency. This study presents a preliminary model for potential further warhead optimization in the context of antibody-directed steroidal glycosides and extends the demonstrated compatibility of aminosugars in the context of neoglycosylation.Entities:
Keywords: Regiochemistry; digitoxigenin; neoglycosylation; sugar
Year: 2015 PMID: 26487911 PMCID: PMC4601055 DOI: 10.1021/acsmedchemlett.5b00120
Source DB: PubMed Journal: ACS Med Chem Lett ISSN: 1948-5875 Impact factor: 4.345