G2138
rac-Glycerol 1-phosphate disodium salt hydrate
≥85% (enzymatic)
Sinonimo/i:
DL-α-Glycerophosphate disodium salt hydrate
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Informazioni su questo articolo
Formula empirica (notazione di Hill):
C3H7Na2O6P · xH2O
Numero CAS:
Peso molecolare:
216.04 (anhydrous basis)
PubChem Substance ID:
UNSPSC Code:
12352201
Beilstein/REAXYS Number:
5177716
MDL number:
assay
≥85% (enzymatic)
storage temp.
2-8°C
SMILES string
O.[Na+].[Na+].OCC(O)COP([O-])([O-])=O
InChI
1S/C3H9O6P.2Na.H2O/c4-1-3(5)2-9-10(6,7)8;;;/h3-5H,1-2H2,(H2,6,7,8);;;1H2/q;2*+1;/p-2
InChI key
OFNNKPAERNWEDD-UHFFFAOYSA-L
Application
rac-Glycerol 1-phosphate does not affect the growth and metabolism of E. coli at concentrations of 5-100μm.
Biochem/physiol Actions
rac-Glycerol 1-phosphate was shown to be produced in mammalian tissues by the hydrolysis of rac-glycerol 1:2-cyclic phosphate by a soluble phosphodiesterase.
Classe di stoccaggio
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Michele Alves-Bezerra et al.
Biochimica et biophysica acta, 1821(12), 1462-1471 (2012-08-21)
Although triacylglycerol (TAG) stores play a critical role in organisms, mechanisms underlying TAG synthesis are poorly understood in invertebrates. In mammals, the synthesis of glycerolipids, including TAG, diacylglycerol (DAG) and phospholipids (PL), occurs predominantly by the glycerol-3-phosphate (G3P) pathway in
Jean-Louis Gallis et al.
Pharmacological research, 65(3), 387-395 (2012-01-10)
The effects of trans-resveratrol (RSV) combined with ethanol (EtOH) were evaluated by (31)P NMR on total ATP and sn-glycerol-3-phosphate (sn-G3P) contents measured in real time in isolated and perfused whole liver of the rat. Mitochondrial ATP turnover was assessed by
Ying Peng et al.
International journal of pharmaceutics, 441(1-2), 482-490 (2012-11-20)
Chitosan/glycerophosphate disodium (GP) thermosensitive hydrogels were prepared for the sustained delivery of venlafaxine hydrochloride (VH) and optimization of this formulation was mainly studied. Release mechanism was investigated by applying various mathematical models to the in vitro release profiles. Overall, drug