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P3637
Phospho(enol)pyruvic acid cyclohexylammonium salt
≥97% (enzymatic)
Synonim(y):
2-(Phosphonooxy)-2-propenoic acid monopotassium salt
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About This Item
Wzór empiryczny (zapis Hilla):
C3H4O6P · C6H14N
Numer CAS:
Masa cząsteczkowa:
267.22
Numer WE:
Numer MDL:
Kod UNSPSC:
12352100
Identyfikator substancji w PubChem:
NACRES:
NA.22
Polecane produkty
Poziom jakości
Próba
≥97% (enzymatic)
Formularz
powder
temp. przechowywania
−20°C
ciąg SMILES
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)
Klucz InChI
VHFCNZDHPABZJO-UHFFFAOYSA-N
Powiązane kategorie
Działania biochem./fizjol.
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.
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Kod klasy składowania
11 - Combustible Solids
Klasa zagrożenia wodnego (WGK)
WGK 3
Temperatura zapłonu (°F)
Not applicable
Temperatura zapłonu (°C)
Not applicable
Środki ochrony indywidualnej
Eyeshields, Gloves, type N95 (US)
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C(4) plants such as corn and sugarcane assimilate atmospheric CO(2) into biomass by means of the C(4) carbon fixation pathway. We asked how PEP formation rate, a key step in the carbon fixation pathway, might work at a precise rate
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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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