New Advances in Chemical Research in 2021. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction by binding to a specific portion of an enzyme and thus slowing or preventing a reaction from occurring. Related Products of 63675-74-1, In an article, mentioned the application of 63675-74-1, Name is 6-Methoxy-2-(4-methoxyphenyl)-1-benzothiophene, molecular formula is C16H14O2S
The crystal and molecular structures of two methoxybenzo[b]thiophenes have been determined by three-dimensional, single-crystal X-ray diffractometry. Both 3-(4?-hydroxy-3?,5?-dimethoxybenzoyl)-2-(4?- methoxyphenyl)-6-methoxybenzo[b]thiophene and 3-(2?,6?-dimethoxybenzoyl)-2-(4?-methoxyphenyl)-6- methoxybenzo[b]thiophene (hereafter referred to as I and II, respectively) crystallize in the monoclinic centrosymmetric space group P21/n (No. 14, C52h) with four formula units-per cell with a = 6.866(1), b = 28.638(2), c = 11.830(2) A, and beta = 105.52(1) and a = 9.328(1), b = 7.977(1), c = 29.650(4) A, and beta = 97.87(1), respectively. The phase problems were solved by direct methods and the respective final full-matrix least-squares refinements converged to R = 0.046 and 0.031. The structures differ in the positioning of the dimethoxy groups of the benzoyl ligands and the addition of a hydroxyl group in I. The molecules in the crystal lattice are held together by van der Waals forces plus the addition of hydrogen bonding in compound I. Selected bond distances and angles and torsion angles are tabularized.
The potential utility of systematic synthetic strategy will be applicable to efficient generations of chemical libraries of compounds to find ‘hit’molecules. Read on for other articles about 63675-74-1
Reference：
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem