SMB00307
Fmoc-L-Thr((Ac)4-α-D-Man)-OH
≥95% (HPLC)
别名:
Fmoc-L-Thr((Ac)4-α-D-Man)-OH, N-α-(9-Fluorenylmethyloxycarbonyl)-O-β-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-L-threonine
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关于此项目
经验公式（希尔记法）:
C33H37NO14
化学文摘社编号:
分子量:
671.65
UNSPSC Code:
12352201
PubChem Substance ID:
NACRES:
NA.22
biological source
synthetic (organic)
assay
≥95% (HPLC)
form
powder
functional group
Fmoc
storage temp.
−20°C
SMILES string
CC(OC[C@H]1O[C@H](OC(C)[C@H](NC(OCC2C3=C(C4=C2C=CC=C4)C=CC=C3)=O)C(O)=O)[C@@H](OC(C)=O)[C@@H](OC(C)=O)[C@@H]1OC(C)=O)=O
InChI
1S/C33H37NO14/c1-16(27(31(39)40)34-33(41)43-14-25-23-12-8-6-10-21(23)22-11-7-9-13-24(22)25)44-32-30(47-20(5)38)29(46-19(4)37)28(45-18(3)36)26(48-32)15-42-17(2)35/h6-13,16,25-30,32H,14-15H2,1-5H3,(H,34,41)(H,39,40)/t16?,26?,27-,28+,29-,30?,32-/m0/s1
InChI key
PTSXZIRHPAUPGC-UHKHZQOWSA-N
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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