Application of 148-51-6In 1974, Morisawa, Yasuhiro;Kataoka, Mitsuru;Watanabe, Taiichiro;Kitano, Noritoshi;Matsuzawa, Toshiaki published 《Anticoccidial agents. 1. Synthesis and anticoccidial activity of 4-deoxypyridoxol and its esters》. 《Journal of Medicinal Chemistry》published the findings. The article contains the following contents:
A series of 21 title compounds were prepared from 3,α4-O-diacetylpyridoxol-HCl [53580-90-8] by hydrogenolysis, followed by hydrolysis and ester formation. In 14 day white Leghorn chicks, moderate activity against Eimeria acervulina was observed for 4-deoxypyridoxol-HCl (I-HCl) [148-51-6], and its diacetate ester-HCl (II-HCl) [53580-95-3], dibutyrate ester-HCl (III-HCl) [53580-96-4], and dihexanoate ester-HCl (IV) [53580-97-5]. The relation of anticoccidial activity to structure and to antivitamin B6 activity was discussed. And 5-(hydroxymethyl)-2,4-dimethylpyridin-3-ol hydrochloride (cas: 148-51-6) was used in the research process.
5-(hydroxymethyl)-2,4-dimethylpyridin-3-ol hydrochloride(cas:148-51-6 Application of 148-51-6) is a vitamin B6 antimetabolite with diverse biological activities. It inhibits transport of pyridoxine , pyridoxal, and pyridoxamine in and reduces growth of S. carlsbergensis cells. DOP inhibits sphingosine-1-phosphate (S1P) lyase and reduces cyclic stretch-induced apoptosis in alveolar epithelial MLE-12 cells.
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