Flexible application of in synthetic route 148-51-6

There are many compounds similar to this compound(148-51-6)Reference of 5-(hydroxymethyl)-2,4-dimethylpyridin-3-ol hydrochloride. if you want to know more, you can check out my other articles. I hope it will help you,maybe you’ll find some useful information.

Reference of 5-(hydroxymethyl)-2,4-dimethylpyridin-3-ol hydrochloride. The protonation of heteroatoms in aromatic heterocycles can be divided into two categories: lone pairs of electrons are in the aromatic ring conjugated system; and lone pairs of electrons do not participate. Compound: 5-(hydroxymethyl)-2,4-dimethylpyridin-3-ol hydrochloride, is researched, Molecular C8H12ClNO2, CAS is 148-51-6, about Preconvulsive changes in brain glucose metabolism following drugs inhibiting glutamate decarboxylase. Author is Horton, R. W.; Meldrum, B. S..

DL-C-allylglycine (I) [7685-44-1], 4-deoxypyridoxine-HCl (II) [148-51-6], and DL-methionine-D-sulfoximine (III) (180, 250, and 300 mg/kg resp., i.p.) each induced preconvulsive increases in the brain glucose [50-99-7] concentration of mice at room temperature; II and III also increased brain glycogen [9005-79-2] concentrations in room-temperature mice, but only II did so in mice maintained at 33-4°. Only with I was the increase in brain glucose concentration associated with an increase in blood glucose concentration I, II, III, or isoniazid [54-85-3] (150 mg/kg) reduced rectal temperature in mice at room temperature but not those at 33-4°. Isoniazid reduced brain glucose and glycogen concentrations in mice at 33-4°, but did not affect mice at room temperature The relation between the effects of these drugs on brain carbohydrates and amino acid metabolism is discussed.

There are many compounds similar to this compound(148-51-6)Reference of 5-(hydroxymethyl)-2,4-dimethylpyridin-3-ol hydrochloride. if you want to know more, you can check out my other articles. I hope it will help you,maybe you’ll find some useful information.

Reference:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia