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Merck
CN

SMB00306

Fmoc-L-Ser((Ac)4-α-D-Man)-OH

≥94% (HPLC)

Synonym(s):

N-α-(9-Fluorenylmethyloxycarbonyl)-O-β-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-L-serine

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About This Item

Empirical Formula (Hill Notation):
C32H35NO14
CAS Number:
118358-80-8
Molecular Weight:
657.62
UNSPSC Code:
12352201
PubChem Substance ID:
329824938
NACRES:
NA.22

Key Documents

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SMILES string

OC([C@@H](NC(OCC1C2=C(C3=C1C=CC=C3)C=CC=C2)=O)CO[C@@H]4[C@@H](OC(C)=O)C(OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O4)=O

InChI

1S/C32H35NO14/c1-16(34)41-15-26-27(44-17(2)35)28(45-18(3)36)29(46-19(4)37)31(47-26)42-14-25(30(38)39)33-32(40)43-13-24-22-11-7-5-9-20(22)21-10-6-8-12-23(21)24/h5-12,24-29,31H,13-15H2,1-4H3,(H,33,40)(H,38,39)/t25-,26?,27+,28?,29+,31-/m0/s1

InChI key

UGQPZVSWEMKXBN-DMRSIPLQSA-N

biological source

synthetic (organic)

assay

≥94% (HPLC)

form

powder

functional group

Fmoc

storage temp.

−20°C

Biochem/physiol Actions

Protein O-mannosylation is an essential modification in fungi and animals. In contrast to most other types of protein O-glycosylation, it is initiated in the endoplasmic reticulum via transfer from dolichol monophosphate-activated mannose.

Storage Class

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
SLBM0136V
SLBN0879V

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