Photoreactive CMP-sialic acids as substrates for α2,6-sialyltransferase

Chemo-enzymatic synthesis afforded a series of CMP-activated sialic acids carrying a photoreactive group at C-9 or C-5, and in part a radiolabel as well. They were found to be accepted by α2,6-sialyltransferase. - Differing amino group reactivity of novel 5,9-diamino sialic acid enabled us to attach...

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Hauptverfasser: Mirelis, Paraskevi (VerfasserIn) , Brossmer, Reinhard (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 7 December 1995
In: Bioorganic & medicinal chemistry letters
Year: 1995, Jahrgang: 5, Heft: 23, Pages: 2809-2814
ISSN:1464-3405
DOI:10.1016/0960-894X(95)00491-B
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1016/0960-894X(95)00491-B
Verlag, lizenzpflichtig, Volltext: https://www.sciencedirect.com/science/article/pii/0960894X9500491B
Volltext
Verfasserangaben:Paraskevi Mirelis, Reinhard Brossmer
Beschreibung
Zusammenfassung:Chemo-enzymatic synthesis afforded a series of CMP-activated sialic acids carrying a photoreactive group at C-9 or C-5, and in part a radiolabel as well. They were found to be accepted by α2,6-sialyltransferase. - Differing amino group reactivity of novel 5,9-diamino sialic acid enabled us to attach sequentially a benzophenone photophore at C-9 and a radiolabel at C-5.
Beschreibung:Elektronische Reproduktion der Druck-Ausgabe 29. März 2000
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Beschreibung:Online Resource
ISSN:1464-3405
DOI:10.1016/0960-894X(95)00491-B