Keolie pyridoxal 5 phosphate,pyridoxal 5'-phosphate



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Keolie pyridoxal 5 phosphate,pyridoxal 5'-phosphate
Keolie pyridoxal 5 phosphate,pyridoxal 5'-phosphate
Keolie pyridoxal 5 phosphate,pyridoxal 5'-phosphate
Keolie pyridoxal 5 phosphate,pyridoxal 5'-phosphate
Keolie pyridoxal 5 phosphate,pyridoxal 5'-phosphate
Keolie pyridoxal 5 phosphate,pyridoxal 5'-phosphate
Keolie pyridoxal 5 phosphate,pyridoxal 5'-phosphate

Keolie pyridoxal 5 phosphate,pyridoxal 5'-phosphate

  • Item No.KL-Pyridoxal-5-phosphate
    MOQ1 Kilogram
Tag  sourcing
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If over 500pcs, mass production will start until pre-production sample has been approved.

Est. 7 days production

Quick Details
Product name Pyridoxal-5-phosphate
Place of Origin CN;SHA
Usage Animal Pharmaceuticals
Brand Name keolie
Appearance White crystalline powder
Model Number KL-Pyridoxal-5-phosphate
Test Method HPLC
molecular weight 247.14
Type Vitamins, Amino Acids and Coenzymes
Grade Standard Food Grade
CAS No. 54-47-7
Melting Point 139 to 142℃
Other Names Pyridoxal-5-phosphate
Density 1.638±0.06 g/cm3
Flash point 296.0±32.9℃

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Quantity(Kilogram) 1 - 100 101 - 1000>1000
Est. Time(days)69To be negotiated

Keolie pyridoxal 5 phosphate,pyridoxal 5'-phosphateintroduce.jpg

Product Name: Pyridoxal-5-phosphate

CAS No:  54-47-7

EINECS No: 200-208-3

Molecular Formular:  C8H10NO6P

Molecular Weight: 247.14

Appearance: White crystalline powder



Pyridoxal phosphate (PLP, pyridoxal 5'-phosphate, P5P), the active form of vitamin B6, is a coenzyme in a variety of enzymatic reactions. The Enzyme commission has catalogued more than 140 PLP-dependent activities, corresponding to ~4% of all classified activities. The versatility of PLP arises from its ability to covalently bind the substrate, and then to act as an electrophilic catalyst, thereby stabilizing different types of carbanionic reaction intermediates.OEM (2)_.jpgfunction.jpg

PLP acts as a coenzyme in all transamination reactions, and in certain decarboxylation, deamination, and racemization reactions of amino acids.The aldehyde group of PLP forms a Schiff-base linkage (internal aldimine) with the ε-amino group of a specific lysine group of the aminotransferase enzyme. The α-amino group of the amino acid substrate displaces the ε-amino group of the active-site lysine residue in a process known as transaldimination. The resulting external aldimine can lose a proton, carbon dioxide, or an amino acid sidechain to become a quinoid intermediate, which in turn can act as a nucleophile in several reaction pathways.
In transamination, after deprotonation the quinoid intermediate accepts a proton at a different position to become a ketimine. The resulting ketimine is hydrolysed so that the amino group remains on the complex.
In addition, PLP is used by aminotransferases (or transaminases) that act upon unusual sugars such as perosamine and desosamine. In these reactions, the PLP reacts with glutamate, which transfers its alpha-amino group to PLP to make pyridoxamine phosphate (PMP). PMP then transfers its nitrogen to the sugar, making an amino sugar.function_.jpg
PLP is also involved in various beta-elimination reactions such as the reactions carried out by serine dehydratase and GDP-4-keto-6-deoxymannose-3-dehydratase (ColD).
It is also active in the condensation reaction in heme synthesis.
PLP plays a role in the conversion of levodopa into dopamine, facilitates the conversion of the excitatory neurotransmitter glutamate to the inhibitory neurotransmitter GABA, and allows SAM to be decarboxylated to form propylamine, which is a precursor to details.jpgcontact.jpgpackage&shipping.jpg

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