| Literature DB >> 28753028 |
Xiang Fei1, Megan E Zavorka2, Guillaume Malik1, Christopher M Connelly2, Richard G MacDonald2, David B Berkowitz1.
Abstract
A generalized strategy is presented for the rapid assembly of a set of bivalent ligands with a variety of linking functionalities from a common monomer. Herein, an array of phosphatase-inert mannose-6-phosphonate-presenting ligands for the cation-independent-mannose 6-phosphate receptor (CI-MPR) is constructed. Receptor binding affinity varies with linking functionality-the simple amide and 1,5-triazole(tetrazole) being preferred over the 1,4-triazole. This approach is expected to find application across chemical biology, particularly in glycoscience, wherein multivalency often governs molecular recognition.Entities:
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Year: 2017 PMID: 28753028 PMCID: PMC6208139 DOI: 10.1021/acs.orglett.7b01914
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005