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About This Item
Empirical Formula (Hill Notation):
C4H10NO6P · xLi+
CAS Number:
Molecular Weight:
199.10 (free acid basis)
UNSPSC Code:
12352209
NACRES:
NA.26
SMILES string
[P](=O)(OCC[C@H](N)C(=O)O)(O)O
InChI
1S/C4H10NO6P/c5-3(4(6)7)1-2-11-12(8,9)10/h3H,1-2,5H2,(H,6,7)(H2,8,9,10)/t3-/m0/s1
InChI key
FXDNYOANAXWZHG-VKHMYHEASA-N
assay
≥95% (TLC)
form
powder
optical activity
[α]/D -18.0±2.0°, c = 1 in H2O
color
white to off-white
storage temp.
−20°C
Quality Level
Related Categories
Biochem/physiol Actions
Metabolite in glycine, serine and threonine metabolism. In higher plants, O-phosphohomoserine represents a branch point between the methionine and threonine biosynthetic pathways.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Hongtao Li et al.
Science (New York, N.Y.), 315(5814), 1000-1003 (2007-02-17)
Pathogenic bacteria use the type III secretion system to deliver effector proteins into host cells to modulate the host signaling pathways. In this study, the Shigella type III effector OspF was shown to inactivate mitogen-activated protein kinases (MAPKs) [extracellular signal-regulated
O Fiehn et al.
Analytical chemistry, 72(15), 3573-3580 (2000-08-22)
Unknown compounds in polar fractions of Arabidopsis thaliana crude leaf extracts were identified on the basis of calculations of elemental compositions obtained from gas chromatography/low-resolution quadrupole mass spectrometric data. Plant metabolites were methoximated and silylated prior to analysis. All known
Oliver Kreft et al.
Plant physiology, 131(4), 1843-1854 (2003-04-15)
In plants, metabolic pathways leading to methionine (Met) and threonine diverge at the level of their common substrate, O-phosphohomoserine (OPHS). To investigate the regulation of this branch point, we engineered transgenic potato (Solanum tuberosum) plants affected in cystathionine gamma-synthase (CgS)
An ATP-independent phosphotransferase in higher plants. The formation of O-phospho-L-homoserine from O-succinyl-L-homoserine and phosphate.
Haginiwa, J., et al.
Chemical & Pharmaceutical Bulletin, 27, 1710-1713 (1979)
Stereochemistry of the hydrogen removal at position 3 in the enzymic synthesis of L-threonine from O-phospho-L-homoserine.
Fuganti, C.
Journal of the Chemical Society. Chemical Communications, 7, 337-339 (1979)
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