Glycerol 2-phosphate
Names
Preferred IUPAC name
1,3-Dihydroxypropan-2-yl dihydrogen phosphate
Other names
1,2,3-Propanetriol, 2-(dihydrogen phosphate) Glycerol 2-phosphate β-Glycerophosphate β-Phosphoglycerol BGP
Identifiers
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard
100.037.465
EC Number
KEGG
MeSH
Beta-glycerophosphoric+acid
UNII
InChI=1S/C3H9O6P/c4-1-3(2-5)9-10(6,7)8/h3-5H,1-2H2,(H2,6,7,8)
Key: DHCLVCXQIBBOPH-UHFFFAOYSA-N
Properties
C 3 H 9 O 6 P
Molar mass
172.073 g·mol−1
Appearance
forms colorless salts
Related compounds
Glycerol 1-phosphate Glycerol 3-phosphate
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
Chemical compound
Glycerol 2-phosphate is the conjugate base of phosphoric ester of glycerol . It is commonly known as β-glycerophosphate or BGP . Unlike glycerol 1-phosphate and glycerol 3-phosphate , this isomer is not chiral. It is also less common.
Applications
β-Glycerophosphate is an inhibitor of the enzyme serine-threonine phosphatase. It is often used in combination with other phosphatase/protease inhibitors for broad spectrum inhibition.[ 1] [ 2]
β-Glycerophosphate is also used to drive osteogenic differentiation of bone marrow stem cells in vitro .[ 3]
β-Glycerophosphate is used to buffer M17 media for Lactococcus culture in recombinant protein expression .[ 4]
Notes