P3637
Phospho(enol)pyruvic acid cyclohexylammonium salt
≥97% (enzymatic)
Synonym(s):
2-(Phosphonooxy)-2-propenoic acid monopotassium salt
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500 MG
$97.37
1 G
$204.00
5 G
$224.00
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500 MG
$97.37
1 G
$204.00
5 G
$224.00
About This Item
Empirical Formula (Hill Notation):
C3H4O6P · C6H14N
CAS Number:
Molecular Weight:
267.22
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
assay
≥97% (enzymatic)
form
powder
storage temp.
−20°C
SMILES string
NC1CCCCC1.OC(=O)C(=C)OP(O)(O)=O
InChI
1S/C6H13N.C3H5O6P/c7-6-4-2-1-3-5-6;1-2(3(4)5)9-10(6,7)8/h6H,1-5,7H2;1H2,(H,4,5)(H2,6,7,8)
InChI key
VHFCNZDHPABZJO-UHFFFAOYSA-N
Related Categories
Biochem/physiol Actions
Phospho(enol)pyruvic acid (PEP) is involved in glycolysis and gluconeogenesis. In glycolysis, PEP is metabolized by pyruvate kinase to yield pyruvate. In plants, PEP is involved in the formation of aromatic amino acids as well as in the carbon fixation pathway.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Journal of bacteriology, 184(1), 152-164 (2001-12-14)
The intracellular carbon flux distribution in wild-type and pyruvate kinase-deficient Escherichia coli was estimated using biosynthetically directed fractional 13C labeling experiments with [U-13C6]glucose in glucose- or ammonia-limited chemostats, two-dimensional nuclear magnetic resonance (NMR) spectroscopy of cellular amino acids, and a
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In many organisms, metabolite interconversion at the phosphoenolpyruvate (PEP)-pyruvate-oxaloacetate node involves a structurally entangled set of reactions that interconnects the major pathways of carbon metabolism and thus, is responsible for the distribution of the carbon flux among catabolism, anabolism and
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