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. Application of 108-47-4,108-47-4, name is 2,4-Dimethylpyridine. In an article，Which mentioned a new discovery about 108-47-4
The self-association of pyridine and some of its alkyl derivatives (2-, 3- and 4-picoline, 2,4- and 2,6-lutidine, 4-tert-butyl- and 2,6-di-tert-butylpyridine) was studied in aqueous solution, at different pH values, by UV spectroscopy.The variation in molar absorptivity with concentration was measured not only for the main maximum, but also for the different component bands of the absorption band in the mid-UV region (above 200 nm) of these compounds.From the experimental curves of hypochromic effects, self-association constants for dimerization (K2) and polymerization (Kn) were calculated.The results obtained are discussed in detail with relation to the position and nature of alkyl substituents on the pyridine ring.The most relevant result is the influence of alkyl substituents on self-association, particularly the special role of the methyl substituents in ortho positions with respect to the nitrogen atom in 2-picoline, 2,4- and 2,6-lutidine.In 2-picoline and 2,6-lutidine, polymerization can be studied separately from dimerization by measuring the band at longest wavelength, which suggests a possible relationship between the mechanism of formation of polymers and the ?* <- n transitions which give rise to these bands.
Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. In my other articles, you can also check out more blogs about 108-47-4
Reference：
Chiral nitrogen ligands in late transition metal-catalysed asymmetric synthesis—I. Addressing the problem of ligand lability in rhodium-catalysed hydrosilations,
Nitrogen-Containing Ligands for Asymmetric Homogeneous and Heterogeneous Catalysis