SMB00306
Fmoc-L-Ser((Ac)4-α-D-Man)-OH
≥94% (HPLC)
别名:
N-α-(9-Fluorenylmethyloxycarbonyl)-O-β-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-L-serine
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关于此项目
经验公式（希尔记法）:
C32H35NO14
化学文摘社编号:
分子量:
657.62
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.22
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.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
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