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Neu5Gcα(2-6) N-Glycan-Asn

Catalog No.: A92360
Glycopeptide
Neu5Gcα(2-6) N-Glycan-Asn is a glycopeptide characterized by its α(2-6) linked sialic acid residue, which is integral to cell recognition and signaling processes. This compound is utilized in biochemical research to investigate glycan-protein interactions, cellular communication, and the role of sialylation in various biological systems. It provides valuable insight into the complexity of glycosylation and its implications in disease mechanisms.
Neu5Gcα(2-6) N-Glycan-Asn 82516-83-4 Glycopeptide
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Research use only. We do not sell to patients.
Data Sheet SDS Compound Handling Instructions

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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
DescriptionNeu5Gcα(2-6) N-Glycan-Asn is a glycopeptide characterized by its α(2-6) linked sialic acid residue, which is integral to cell recognition and signaling processes. This compound is utilized in biochemical research to investigate glycan-protein interactions, cellular communication, and the role of sialylation in various biological systems. It provides valuable insight into the complexity of glycosylation and its implications in disease mechanisms.
Product Information
Catalog NumA92360
FormulaC88H144N8O66
Molecular Weight2370.10
CAS Number82516-83-4
SMILESOC[C@H]([C@H]1O[C@H](O[C@@H]2CO[C@@]3(C(O)=O)O[C@@]([H])([C@@H]([C@@H](CO)O)O)[C@H](NC(CO)=O)[C@@H](O)C3)[C@H](O)[C@@H](O)[C@H]2O)O[C@@H](O[C@@H]4[C@@H](O[C@@H]5[C@H](O)[C@H](O[C@@H]6[C@@H](CO)O[C@@H](O[C@@H]7[C@@H](CO)O[C@@H](NC(C[C@@H](C(O)=O)N)=O)[C@H](NC(C)=O)[C@H]7O)[C@H](NC(C)=O)[C@H]6O)O[C@H](CO[C@@H]8[C@@H](O[C@H]9[C@H](NC(C)=O)[C@@H](O)[C@H](O[C@@H]%10O[C@H](CO[C@@]%11(C(O)=O)O[C@@]([H])([C@@H]([C@@H](CO)O)O)[C@H](NC(CO)=O)[C@@H](O)C%11)[C@H](O)[C@H](O)[C@H]%10O)[C@@H](CO)O9)[C@@H](O)[C@H](O)[C@@H](CO)O8)[C@H]5O)O[C@H](CO)[C@@H](O)[C@@H]4O)[C@H](NC(C)=O)[C@H]1O
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