Pyridoxal phosphate


CAS No. : 54-47-7

(Synonyms: Pyridoxal 5′-phosphate; Pyridoxyl phosphate)

54-47-7
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Cat. No. : HY-B1744
M.Wt: 247.14
Formula: C8H10NO6P
Purity: >98 %
Solubility: H2O : 5 mg/mL (ultrasonic);DMSO : 62.5 mg/mL (ultrasonic;warming;heat to 60°C)
Introduction of 54-47-7 :

Pyridoxal phosphate is the active form of vitamin B6, acts as an inhibitor of reverse transcriptases, and is used for the treatment of tardive dyskinesia. In Vitro:Pyridoxal 5′-phosphate severely inhibits the DNA Polymerase and RNase H. Pyridoxal phosphate results in an imnediate reduction in the rate of DNA synthesis[1]. Conjugation to pyridoxal phosphate fully inhibits NEIL2. Pyridoxal phosphate-conjugated NEIL2 shows much lower activity than the intact enzyme over a wide range of enzyme/substrate ratios. After Pyridoxal phosphate conjugation, the ability of NEIL2 to bind the THF-ligand is completely lost[2]. Pyridoxal phosphate (500 μM, 24 h) activates the ERK/c-Jun signaling pathway, promotes the expression of IGFBP1 protein in HepG2 cells[3].
Pyridoxal phosphate (0.5 mg/mL, 48h) inhibits the proliferation of cancer cells SK-OV-3 and OVCAR-3[5].
In Vivo:Pyridoxal phosphate (1 mg/kg, ip, single dose) alleviates Aβ25-35-induced spatial memory impairment and long-term memory impairment in mouse models[4].
Pyridoxal phosphate (600 mg/kg/day, po for 16 weeks) inhibits the formation of advanced glycation end-products (AGEs), and prevents the progression of diabetic nephropathy in Streptozotocin (HY-13753)-induced rats diabetes model[6].

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