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3913-50-6

3913-50-6 Structure

3913-50-6 Structure
IdentificationBack Directory
[Name]

3-HYDROXY-2,2-DIMETHOXY-PROPANOIC ACID 3-PHOSPHATE TRI(CYCLOHEXYLAMMONIUM) SALT
[CAS]

3913-50-6
[Synonyms]

3 phosphohydroxypyruvate
3-phosphonooxypyruvicaci
Phosphohydroxypyruvic acid
3-phosphonooxypyruvic acid
3-Phosphohydroxypyruvic acid
Phosphohydroxypyruvic acid, 98+%
2-oxo-3-phosphonooxy-propanoic acid
2,2-dimethoxypropanoic acid 3-phosphate
Hydroxypyruvic acid phosphate lithium salt
hydroxypyruvic acid dimethylketal*phosphate
cyclohexanamine 2,2-dimethoxy-3-(phosphonatooxy)propanoate
HYDROXYPYRUVIC ACID DIMETHYLKETAL PHOSPHATE TRI(CYCLOHEXYLAMMONIUM) SALT
3-HYDROXY-2,2-DIMETHOXY-PROPANOIC ACID 3-PHOSPHATE TRI(CYCLOHEXYLAMMONIUM) SALT
[Molecular Formula]

C3H5O7P
[MDL Number]

MFCD00058333
[MOL File]

3913-50-6.mol
[Molecular Weight]

184.04
Chemical PropertiesBack Directory
[Boiling point ]

432.4±47.0 °C(Predicted)
[density ]

1.930
[storage temp. ]

−20°C
[pka]

1.58±0.10(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302+H312
[Precautionary statements ]

P264-P270-P280-P301+P312-P302+P352+P312-P362+P364
[Hazard Codes ]

Xn
[Risk Statements ]

21/22
[Safety Statements ]

36/37
[RIDADR ]

UN 2811 6.1/PG 3
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

3-Hydroxy-2,2-dimethoxy-propanoic Acid-3-phosphatetri(cyclohexylammonium) Salt is used in the preparation of mTORC1 signaling agents that activates ATF.
[Definition]

ChEBI: A carboxyalkyl phosphate that is pyruvic acid substituted at position 3 by a 3-phosphonooxy group.
[Biological Activity]

L-Serine may be derived from four possible sources: dietary intakebiosynthesis from the glycolytic intermediate 3-phosphoglyceratefrom glycineand by protein and phospholipid degradation. In the biosynthetic pathwaythe glycolytic intermediate 3-phosphoglycerate is converted into phosphohydroxy-pyruvatein a reaction catalyzed by 3-phosphoglycerate dehydrogenase (3- PGDH; EC 1.1.1.95). Phosphohydroxypyruvate is metabolized to phosphoserine by phosphohydroxypyruvate aminotransferase (EC 2.6.1.52) andfinallyphosphoserine is converted into L-serine by phosphoserine phosphatase (PSP; EC 3.1.3.3). In liver tissuethe serine biosynthetic pathway is regulated in response to dietary and hormonal changes. Of the three synthetic enzymesthe properties of 3-PGDH and PSP are the best documented. Hormonal factors such as glucagon and corticosteroids also influence 3-PGDH and PSP activities in interactions dependent upon the diet. L-serine plays a central role in cellular proliferatio
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