UDP-GlcNAz

Catalog No.: A75097
Sugar Donor
UDP-GlcNAz serves as an analog of UDP-GlcNAc, functioning primarily as a sugar donor substrate for N-acetylgalactosaminyltransferases. These enzymes utilize UDP-GlcNAz to transfer N-acetylglucosamine to saccharide or peptide acceptors. Featuring an azide group, UDP-GlcNAz is also a valuable click chemistry reagent, enabling copper-catalyzed azide-alkyne cycloaddition (CuAAc) and strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with alkyne-containing molecules. Its versatility makes it suitable for various applications in chemical biology and glycobiology research.
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5mg
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50mg
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Adooq Products cited in reputable paper
Science VOLUME 380, ISSUE 6663 (2023)
Science VOLUME 369, ISSUE 6510 (2020)
Science VOLUME 356, ISSUE 6336 (2017)
Cell Vol. 185 Issue 23 p4428-4447.e28
Cell Vol 177, Issue 7, p1933-1947.e25
Cell Vol 156, Issue 5, p857-1114
Nature Volume 622 Issue 7982 (2023)
Nature volume 620, pages890-897 (2023)
Nature volume 610, pages540-546 (2022)
Nature volume 588, pages83-88 (2020)
Nature volume 574, pages268-272 (2019)
Nature volume 573, pages539-545 (2019)
Nature volume 567, pages118-122 (2019)
Nature volume 551, pages639-643 (2017)
Nature volume 551, pages247-250 (2017)
Nature volume 548, pages356-360 (2017)
Nature volume 545, pages187-192 (2017)
Biological Activity
DescriptionUDP-GlcNAz serves as an analog of UDP-GlcNAc, functioning primarily as a sugar donor substrate for N-acetylgalactosaminyltransferases. These enzymes utilize UDP-GlcNAz to transfer N-acetylglucosamine to saccharide or peptide acceptors. Featuring an azide group, UDP-GlcNAz is also a valuable click chemistry reagent, enabling copper-catalyzed azide-alkyne cycloaddition (CuAAc) and strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with alkyne-containing molecules. Its versatility makes it suitable for various applications in chemical biology and glycobiology research.
Product Information
Catalog NumA75097
FormulaC17H26N6O17P2
Molecular Weight648.37
CAS Number608514-41-6
SMILESO=C(C=CN1[C@H]2[C@H](O)[C@H](O)[C@@H](COP(OP(O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@H]3NC(CN=[N+]=[N-])=O)(O)=O)(O)=O)O2)NC1=O
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