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Merck
CN

C8286

Cellotetraose

≥85% (HPLC)

别名:

(β-D-Glc-[1→4])3-D-Glc, D-(+)-Cellotetraose

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关于此项目

经验公式（希尔记法）:
C24H42O21
化学文摘社编号:
38819-01-1
分子量:
666.58
UNSPSC Code:
12352201
NACRES:
NA.25
PubChem Substance ID:
24893043
MDL number:
MFCD00079079
Beilstein/REAXYS Number:
78869

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产品名称

Cellotetraose, ≥85% (HPLC)

InChI key

LUEWUZLMQUOBSB-YQGOCCRESA-N

SMILES string

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

InChI

1S/C24H42O21/c25-1-5-9(29)10(30)15(35)22(40-5)44-19-7(3-27)42-24(17(37)12(19)32)45-20-8(4-28)41-23(16(36)13(20)33)43-18-6(2-26)39-21(38)14(34)11(18)31/h5-38H,1-4H2/t5-,6-,7-,8-,9-,10+,11-,12-,13-,14-,15-,16-,17-,18-,19-,20-,21?,22+,23+,24+/m1/s1

biological source

synthetic (organic)

assay

≥85% (HPLC)

form

powder

color

white

solubility

water: 25 mg/mL, clear, colorless to faintly yellow

storage temp.

−20°C

Quality Level

200

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相关类别

Application

Cellotetraose is a 4-glucose polymer cellulodextrin derived from cellulose degradation. Cellotetraose and other cellulodextrins, such as cellulobiose, cellulotriose and cellopentaose are used by cellulosic bacteria as sources of energy. Cellotetraose is used to help identify, differentiate and characterize oligosaccharide metabolizing enzymes.

Biochem/physiol Actions

Cellotetraose is a substrate for many cellulases and for 1,4-β-D-glucan glucohydrolases. It is also the end product of some cellulases, such as Cel9R from Clostridium thermocellum.

Other Notes

To gain a comprehensive understanding of our extensive range of Polysaccharides for your research, we encourage you to visit our Carbohydrates Category page.

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

涉药品监管产品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
SLCQ4671
SLCR4055
SLCQ8594
SLCQ6432
SLCG2602

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Yuko Yoneda et al.
Journal of the American Chemical Society, 130(49), 16678-16690 (2009-06-26)
Hydrogen bonding is important in cellulosic and other carbohydrate structures, but the role of interactions between nonpolar groups is less understood. Therefore, we synthesized cyclohexyl 4'-O cyclohexyl beta-D-cellobioside (8), a molecule that has two glucose rings and two nonpolar cyclohexyl
Elizabeth A Znameroski et al.
Proceedings of the National Academy of Sciences of the United States of America, 109(16), 6012-6017 (2012-04-05)
Neurospora crassa colonizes burnt grasslands in the wild and metabolizes both cellulose and hemicellulose from plant cell walls. When switched from a favored carbon source such as sucrose to cellulose, N. crassa dramatically upregulates expression and secretion of a wide
Hitoshi Suzuki et al.
Applied and environmental microbiology, 76(18), 6164-6170 (2010-07-27)
The wood decay basidiomycete Phanerochaete chrysosporium produces a variety of cellobiohydrolases belonging to glycoside hydrolase (GH) families 6 and 7 in the presence of cellulose. However, no inducer of the production of these enzymes has yet been identified. Here, we
Takuji Oyama et al.
PloS one, 8(11), e80448-e80448 (2013-11-28)
CpMan5B is a glycoside hydrolase (GH) family 5 enzyme exhibiting both β-1,4-mannosidic and β-1,4-glucosidic cleavage activities. To provide insight into the amino acid residues that contribute to catalysis and substrate specificity, we solved the structure of CpMan5B at 1.6 Å
Ya-Shan Cheng et al.
Biochimica et biophysica acta, 1844(2), 366-373 (2013-11-23)
The thermostable 1,3-1,4-β-glucanase PtLic16A from the fungus Paecilomyces thermophila catalyzes stringent hydrolysis of barley β-glucan and lichenan with an outstanding efficiency and has great potential for broad industrial applications. Here, we report the crystal structures of PtLic16A and an inactive
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