Gil, D. L. published the artcileStructure-activity relationships of 1,2,3-benzothiadiazole insecticide synergists as inhibitors of microsomal oxidation, HPLC of Formula: 1753-29-3, the publication is Pesticide Biochemistry and Physiology (1977), 7(2), 183-93, database is CAplus.
The activities of 47 substituted 1,2,3-benzothiadiazoles (I) as inhibitors of microsomal epoxidation and/or hydroxylation in enzyme preparations from rat liver or armyworm (Spodoptera eridania) gut have been evaluated. Many were found to be effective inhibitors of microsomal oxidation, the most active being the 6-butyl [60474-26-2] and 6-propoxy [63226-45-9] derivatives with I50 values of 4.9 × 10-7 and 7.0 × 10-7 M, resp., for the epoxidation reaction. Regression anal. have established that activity of the 5-, 6-, and 5,6-substituted compounds can be satisfactorily described in equations in terms of π2, π, and σ whereas that of the 4-substituted derivatives depends on π and the steric parameter Es.
Pesticide Biochemistry and Physiology published new progress about 1753-29-3. 1753-29-3 belongs to thiazole, auxiliary class Other Aromatic Heterocyclic,Amine, name is Benzo[d][1,2,3]thiadiazol-5-amine, and the molecular formula is C6H5N3S, HPLC of Formula: 1753-29-3.
Referemce:
https://pubchem.ncbi.nlm.nih.gov/compound/thiazole,
Thiazole | chemical compound | Britannica