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
生物来源
synthetic (organic)
方案
≥94% (HPLC)
表单
powder
官能团
Fmoc
储存温度
−20°C
SMILES字符串
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
生化/生理作用
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.
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
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