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GalNAc-NAG15 phosphoramidite

Catalog No.: A89641
Phosphoramidite Derivative
GalNAc-NAG15 phosphoramidite is a phosphoramidite derivative featuring N-acetylgalactosamine (GalNAc) linked to N-acetylglucosamine (NAG). This compound serves as a key building block for the synthesis of oligonucleotides, enabling the incorporation of GalNAc for applications in glycobiology and gene delivery research. Its unique structural properties facilitate the study of glycan interactions and the development of glyco-engineered therapeutics.
GalNAc-NAG15 phosphoramidite 2920438-06-6 Phosphoramidite Derivative
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Research use only. We do not sell to patients.
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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
DescriptionGalNAc-NAG15 phosphoramidite is a phosphoramidite derivative featuring N-acetylgalactosamine (GalNAc) linked to N-acetylglucosamine (NAG). This compound serves as a key building block for the synthesis of oligonucleotides, enabling the incorporation of GalNAc for applications in glycobiology and gene delivery research. Its unique structural properties facilitate the study of glycan interactions and the development of glyco-engineered therapeutics.
Product Information
Catalog NumA89641
FormulaC82H132N11O37P
Molecular Weight1894.95
CAS Number2920438-06-6
SMILESCC(O[C@H]1[C@H]([C@H](O[C@H]([C@@H]1NC(C)=O)OCCOCCNC(CN(C(CCCC(N2CCC(CC2)OP(OCCC#N)N(C(C)C)C(C)C)=O)=O)CCCN(CC(NCCOCCO[C@H]3[C@@H]([C@H]([C@H]([C@H](O3)COC(C)=O)OC(C)=O)OC(C)=O)NC(C)=O)=O)CC(NCCOCCO[C@H]4[C@@H]([C@H]([C@H]([C@H](O4)COC(C)=O)OC(C)=O)OC(C)=O)NC(C)=O)=O)=O)COC(C)=O)OC(C)=O)=O
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