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Merck
CN

G9380

α- D -葡萄糖 1-磷酸盐 二钠盐 水合物

98-99%

别名:

α-D-葡吡喃糖-1-磷酸, 山梨醇酯

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关于此项目

线性分子式:
C6H11O9PNa2 · xH2O
化学文摘社编号:
分子量:
304.10 (anhydrous basis)
UNSPSC Code:
12352201
PubChem Substance ID:
EC Number:
260-154-1
MDL number:
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assay

98-99%

form

powder

technique(s)

thin layer chromatography (TLC): suitable

impurities

α-D-glucose 1,6-diphosphate, glucose and starch, essentially free

storage temp.

−20°C

SMILES string

[Na+].[Na+].[H]O[H].OC[C@H]1O[C@H](OP([O-])([O-])=O)[C@H](O)[C@@H](O)[C@@H]1O

InChI

1S/C6H13O9P.2Na.H2O/c7-1-2-3(8)4(9)5(10)6(14-2)15-16(11,12)13;;;/h2-10H,1H2,(H2,11,12,13);;;1H2/q;2*+1;/p-2/t2-,3-,4+,5-,6-;;;/m1.../s1

InChI key

YWAUQXHOCBBYLP-FBNUBEQJSA-L

General description

α-D-葡萄糖 1-磷酸在磷酸葡萄糖变位酶作用下转化为 D-葡萄糖-6-磷酸。


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存储类别

13 - Non 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

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历史批次信息供参考:

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Lot/Batch Number

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Joerg Fettke et al.
Plant physiology, 155(4), 1723-1734 (2010-12-01)
Almost all glucosyl transfer reactions rely on glucose-1-phosphate (Glc-1-P) that either immediately acts as glucosyl donor or as substrate for the synthesis of the more widely used Glc dinucleotides, ADPglucose or UDPglucose. In this communication, we have analyzed two Glc-1-P-related
Stanley A Blumenthal
Perspectives in biology and medicine, 55(2), 236-249 (2012-05-31)
In 1945, Earl Sutherland (1915-1974) [corrected] and associates began studies of the mechanism of hormone-induced glycogen breakdown in the liver. In 1956, their efforts culminated in the identification of cyclic AMP, an ancient molecule generated in many cell types in
Ting Yang et al.
The Biochemical journal, 429(3), 533-543 (2010-05-21)
The diverse types of glycoconjugates synthesized by trypanosomatid parasites are unique compared with the host cells. These glycans are required for the parasite survival, invasion or evasion of the host immune system. Synthesis of those glycoconjugates requires a constant supply



全球贸易项目编号

货号GTIN
G9380-100MG04061832390536