α-D-Glucose 1-phosphate disodium salt
CAS No. 56401-20-8
α-D-Glucose 1-phosphate disodium salt ( α-D-Glucopyranose 1-phosphate )
Catalog No. M19703 CAS No. 56401-20-8
α-D-Glucose 1-phosphate disodium salt is converted into D-glucose-6-phosphate by the enzyme phosphoglucomutase.
Purity : >98% (HPLC)
Size | Price / USD | Stock | Quantity |
50MG | 30 | In Stock |
|
100MG | 36 | In Stock |
|
200MG | 53 | In Stock |
|
500MG | Get Quote | In Stock |
|
1G | Get Quote | In Stock |
|
Biological Information
-
Product Nameα-D-Glucose 1-phosphate disodium salt
-
NoteResearch use only, not for human use.
-
Brief Descriptionα-D-Glucose 1-phosphate disodium salt is converted into D-glucose-6-phosphate by the enzyme phosphoglucomutase.
-
Descriptionα-D-Glucose 1-phosphate disodium salt is converted into D-glucose-6-phosphate by the enzyme phosphoglucomutase.
-
In Vitro——
-
In Vivo——
-
Synonymsα-D-Glucopyranose 1-phosphate
-
PathwayOthers
-
TargetOther Targets
-
RecptorOthers
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number56401-20-8
-
Formula Weight322.11
-
Molecular FormulaC6H13Na2O10P
-
Purity>98% (HPLC)
-
SolubilityDMSO:10 mM
-
SMILESO.[Na+].[Na+].OC[C@H]1O[C@H](OP([O-])([O-])=O)[C@H](O)[C@@H](O)[C@@H]1O
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
-
Cyclo(Tyr-Pro)
Cyclo(Tyr-Pro) shows antibacterial activity towards several marine bacterial species, it also shows weak antagonistic activity against VEGFR2 -CD. Cyclo(Tyr-Pro) and cyclo(Pro-Val) are toxic to both suspension cells and seedlings of Pinus thunbergii, which may offer some clues to research the mechanism of pine wilt disease caused by pine wood nematode.
-
Alisol C monoacetate
Alisol C 23-acetate is a natural product isolated from Alisma orientale, can significantly and strongly inhibit DTH response after oral administration,has antibacterial activity.
-
CITCO
CITCO inhibits growth and expansion of brain tumour stem cells (BTSCs) and has an EC50 of 49?nM over pregnane X receptor (PXR), and no activity on other nuclear receptors.