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Merck
CN

M0925

3α,6α-Mannopentaose

≥85%

Synonym(s):

α-Man-(1→3)(α-Man-[1→6])-α-Man-(1→6)(α-Man-[1→3])-Man

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About This Item

Empirical Formula (Hill Notation):
C30H52O26
CAS Number:
112828-69-0
Molecular Weight:
828.72
NACRES:
NA.32
PubChem Substance ID:
329817839
UNSPSC Code:
12352200
MDL number:
MFCD01310886

Key Documents

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Product Name

3α,6α-Mannopentaose, ≥85%

InChI

1S/C30H52O26/c31-1-7(35)25(55-29-22(46)19(43)15(39)10(3-33)52-29)13(37)8(36)5-49-28-24(48)26(56-30-23(47)20(44)16(40)11(4-34)53-30)17(41)12(54-28)6-50-27-21(45)18(42)14(38)9(2-32)51-27/h1,7-30,32-48H,2-6H2/t7-,8-,9-,10-,11-,12-,13-,14-,15-,16-,17-,18+,19+,20+,21+,22+,23+,24+,25-,26+,27+,28+,29-,30-/m1/s1

SMILES string

OC[C@H]1O[C@H](OC[C@H]2O[C@H](OC[C@@H](O)[C@@H](O)[C@H](O[C@H]3O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]3O)[C@H](O)C=O)[C@@H](O)[C@@H](O[C@H]4O[C@H](CO)[C@@H](O)[C@H](O)[C@@H]4O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O

InChI key

YPQGRSSAXDUGEC-LHCUGFEVSA-N

assay

≥85%

storage temp.

2-8°C

Quality Level

200

Related Categories

Application

3α,6α-Mannopentaose has been used:
  • in the modification of six valent osmium complexes with N,N,N′,N′-tetramethylethylenediamine (Os(VI)tem) for voltammetric analysis
  • to study the structure of Burkholderia oklahomensis EO147 agglutinin (BOA)
  • as a commercial isomeric oligosaccharide in matrix-assisted laser desorption/ionization (MALDI) LTQ orbitrap fragmentation studies

General description

Core structure of some triantennary N-linked oligosaccharides

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

涉药品监管产品
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Certificates of Analysis (COA)

Lot/Batch Number
0000481139
0000481139
0000478400
0000478400
SLCP6996

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Matthew J Whitley et al.
The FEBS journal, 280(9), 2056-2067 (2013-03-14)
Burkholderia oklahomensis EO147 agglutinin (BOA) is a 29 kDa member of the Oscillatoria agardhii agglutinin (OAA) family of lectins. Members of the OAA family recognize high-mannose glycans, and, by binding to the HIV envelope glycoprotein 120 (gp120), block the virus
Mojmír Trefulka et al.
Bioelectrochemistry (Amsterdam, Netherlands), 133, 107494-107494 (2020-03-03)
Compounds containing vicinal diol (glycol) groups, including saccharides, could be modified with sixvalent osmium complexes with nitrogenous ligands, particularly with N,N,N',N'-tetramethylethylenediamine (Os(VI)tem). The modification products are electrochemically active. Here we show that aminosaccharides can also be modified by Os(VI)tem. We
Fragmentation of neutral oligosaccharides using the MALDI LTQ Orbitrap
Rohmer M, et al.
International Journal of Mass Spectrometry, 305(2-3), 199-208 (2011)

Articles

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N-连接聚糖、修饰和降解

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