Dephosphorylation of pyridoxal 5′-phosphate-derived Schiff bases in the presence of bovine alkaline phosphatase was written by Gamov, George;Murekhina, Anastasia;Aleksandriiskii, Viktor. And the article was included in International Journal of Chemical Kinetics in 2022.Application of 54-47-7 The following contents are mentioned in the article:
The present paper reports on the study of the dephosphorylation of pyridoxal 5′-phosphate and four derived hydrazones (containing the residues of pyrazine, 2-furan, 2-thiophene, 3-pyridine carboxylic acids) induced by bovine alk. phosphatase from intestinal mucosa at 298.2 K and pH 10 (0.05 m Tris-HCl buffer). We observed and discussed characteristic changes in the UV-vis and fluorescent spectra of substrates. Michaelis-Menten parameters of the enzymic dephosphorylation are calculated The stability of alk. phosphatase in the presence of hydrazones is confirmed. The dephosphorylation of the Zn(II) complex with pyridoxal 5′-phosphate-derived hydrazone is analyzed. This study involved multiple reactions and reactants, such as (4-Formyl-5-hydroxy-6-methylpyridin-3-yl)methyl dihydrogen phosphate (cas: 54-47-7Application of 54-47-7).
(4-Formyl-5-hydroxy-6-methylpyridin-3-yl)methyl dihydrogen phosphate (cas: 54-47-7) belongs to pyridine derivatives. Pyridine has a conjugated system of six 蟺 electrons that are delocalized over the ring. The molecule is planar and, thus, follows the H眉ckel criteria for aromatic systems. Many analogues of pyridine are known where N is replaced by other heteroatoms . Substitution of one C鈥揌 in pyridine with a second N gives rise to the diazine heterocycles (C4H4N2), with the names pyridazine, pyrimidine, and pyrazine.Application of 54-47-7