Tricyclohexanaminium 2-(phosphonatooxy)acrylate

Names

[ Name ]:
Tricyclohexanaminium 2-(phosphonatooxy)acrylate

[Synonym ]:
PEP TRICYCLOHEXYL-AMMONIUM SALT
2-Propenoic acid, 2-(phosphonooxy)-, compd. with cyclohexanamine (1:3)
cyclohexylamine,salt of/the/ 2-phosphonooxy-acrylic acid
2-(Phosphonooxy)acrylic acid - cyclohexanamine (1:3)
PHOSPHOENOLPYRUVATE TRIS(CYCLOHEXYLAMMONIUM) SALT
tri(cyclohexyl amine) salt
PHOSPHOENOLPYRUVIC ACID TRIS(CYCLOHEXYLAMINE) SALT
2-(phosphonooxy)acrylic acid
EINECS 252-618-7
PEP-TRI
PHOSPHO(ENOL)PYRUVATE*TRI(CYCLOHEXYLAMMO NIUM)
compound with cyclohexylamine (1:3)
phosphoenolpyruvic acid
PEP-3CHA
Tricyclohexanaminium 2-(phosphonatooxy)acrylate
PEP
PEP TCHA SALT
PHOSPHOENOLPYRUVIC ACID TRI(CYCLOHEXYLAMINE) SALT
Cyclohexylamin,Salz der 2-Phosphonooxy-acrylsaeure
MFCD00004258
Phosphoenolpyruvic Acid Tris(cyclohexylaMMoniuM) Salt Hydrate
PEP 3 CHX

Biological Activity

[Description]:

Phosphoenolpyruvic acid tricyclohexylammonium salt is a glycolysis metabolite with a high-energy phosphate group, penetrates the cell membrane and exhibits cytoprotective and anti-oxidative activity[1].

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

[References]

[1]. Kondo Y, et al. Phosphoenolpyruvic acid, an intermediary metabolite of glycolysis, as a potential cytoprotectant and anti-oxidant in HeLa cells. Biol Pharm Bull. 2012;35(4):606-11.

Chemical & Physical Properties

[ Boiling Point ]:
466.7ºC at 760 mmHg

[ Melting Point ]:
197-198 °C

[ Molecular Formula ]:
C₂₁H₄₄N₃O₆P

[ Molecular Weight ]:
465.564

[ Flash Point ]:
236.1ºC

[ Exact Mass ]:
465.296783

[ PSA ]:
205.28000

[ LogP ]:
0.91870

[ Storage condition ]:
2-8°C

MSDS

Click to get detail MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Safety Phrases ]:
S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Articles

The PEP-pyruvate-oxaloacetate node as the switch point for carbon flux distribution in bacteria.

FEMS Microbiol. Rev. 29(4) , 765-94, (2005)

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 ca...

Inducer exclusion in Escherichia coli by non-PTS substrates: the role of the PEP to pyruvate ratio in determining the phosphorylation state of enzyme IIAGlc.

Mol. Microbiol. 30(3) , 487-98, (1998)

The main mechanism causing catabolite repression in Escherichia coli is the dephosphorylation of enzyme IIAGlc, one of the enzymes of the phosphoenolpyruvate:carbohydrate phosphotransferase system (PT...

Metabolic flux responses to pyruvate kinase knockout in Escherichia coli.

J. Bacteriol. 184(1) , 152-64, (2002)

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]gl...

Related Compounds

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