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Safety Information

SMB00299

Sigma-Aldrich

Fmoc-L-Ser((Ac)3-β-D-GlcNAc)-OH

≥95% (HPLC)

Synonym(s):

Fmoc-L-Ser((Ac)3-β-D-GlcNAc)-OH, N-α-(9-Fluorenylmethyloxycarbonyl)-O-β-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)-L-serine

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About This Item

Empirical Formula (Hill Notation):
C32H36N2O13
CAS Number:
160067-63-0
Molecular Weight:
656.63
UNSPSC Code:
12352201
PubChem Substance ID:
329824931
NACRES:
NA.22

Assay

≥95% (HPLC)

form

powder

functional group

Fmoc

storage temp.

−20°C

SMILES string

[R]C[C@H]1O[C@@H](OC[C@@H](NC(OCC2C3=C(C4=C2C=CC=C4)C=CC=C3)=O)C(O)=O)[C@H](NC(C)=O)C([R])[C@@H]1[R]

InChI

1S/C32H36N2O13/c1-16(35)33-27-29(46-19(4)38)28(45-18(3)37)26(15-42-17(2)36)47-31(27)43-14-25(30(39)40)34-32(41)44-13-24-22-11-7-5-9-20(22)21-10-6-8-12-23(21)24/h5-12,24-29,31H,13-15H2,1-4H3,(H,33,35)(H,34,41)(H,39,40)/t25-,26+,27+,28+,29+,31+/m0/s1

InChI key

ORICVOOXZDVFIP-ILRBKQRBSA-N

General description

A basic monosaccharide fragment of branched N-linked oligosaccharides found on glycoproteins.

Biochem/physiol Actions

In dynamic protein glycosylation, reversible O-GlcNAc modification of nuclear and cytoplasmic proteins at serine and threonine controls diverse aspects of cell physiology and is conceptually analogous to phosphorylation.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
SLBL0552V

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