Inhibitors of hepatic mixed function oxidases. V. Inhibition of aminopyrine N-demethylation and enhancement of aniline hydroxylation by benzoxazole derivatives was written by Little, Peter J.;Ryan, Adrian J.. And the article was included in Biochemical Pharmacology in 1982.Recommanded Product: 5676-58-4 This article mentions the following:
All of a series of 12 benzoxazoles tested inhibited aminopyrine N-demethylase (I) activity of rat liver microsomes from phenobarbitone-treated rats, and there was an apparent relation between inhibitory potency and partition coefficient For the 2-alkylbenzoxazole series, inhibitory potency towards I activity increased as the number of C atoms in the alkyl side chain increased. Substitution of a Me group into the 2 or 5 position of the benzoxazole nucleus produced a 2- to 3-fold increase in inhibitory potential for each instance. Eleven of the benzoxazoles enhanced aniline p-hydroxylase activity in rat liver microsomes, whereas one, zoxazolamine, was inhibitory; no relation was apparent between physicochem. properties and degree of enhancement of aniline p-hydroxylase activity. In the experiment, the researchers used many compounds, for example, 2,5-Dimethylbenzoxazole (cas: 5676-58-4Recommanded Product: 5676-58-4).
2,5-Dimethylbenzoxazole (cas: 5676-58-4) belongs to benzoxazole derivatives. Benzoxazole derivatives have gained a lot of importance in the past few years because of their use in intermediates for the preparation of new biological materials. It is found within the chemical structures of pharmaceutical drugs such as flunoxaprofen and tafamidis.Recommanded Product: 5676-58-4
Referemce:
Benzoxazole – Wikipedia,
Benzoxazole | C7H5NO – PubChem