Enzyme-inducing effects of salicylate derivatives was written by Goudonnet, Herve;Mounie, Jacques;Bereksi-Reguig, K.;Truchot, Roger. And the article was included in Comptes Rendus des Seances de la Societe de Biologie et de Ses Filiales in 1982.Quality Control of 4-Acetamidophenyl 2-acetoxybenzoate The following contents are mentioned in the article:
Of the salicylate derivatives examined, salicylic acid [69-72-7] itself, Me salicylate [119-36-8], salicylazosulfapyridine [599-79-1], 4-iodosalicylic acid [16870-28-3], and acetylsalicylic acid [50-78-2] appeared not to induce liver microsomal enzymes in rats, while salicylamide (I) [65-45-2] and benorylate (II) [5003-48-5] caused significant induction, and 3,5-diiodosalicylic acid (III) [133-91-5] was an extremely potent inducer. After 3 daily oral 125-mg/kg doses of III, for example, liver microsomal cytochrome P 450 activity was doubled. Structure-activity relations are briefly discussed. This study involved multiple reactions and reactants, such as 4-Acetamidophenyl 2-acetoxybenzoate (cas: 5003-48-5Quality Control of 4-Acetamidophenyl 2-acetoxybenzoate).
4-Acetamidophenyl 2-acetoxybenzoate (cas: 5003-48-5) belongs to esters. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Cyclic esters are called lactones, regardless of whether they are derived from an organic or inorganic acid. One example of an organic lactone is γ-valerolactone.Quality Control of 4-Acetamidophenyl 2-acetoxybenzoate
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics