Application of 24621-61-2, 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. In a document type is Article, and a compound is mentioned, 24621-61-2, Name is (S)-Butane-1,3-diol, introducing its new discovery.
beta-Galactosyl transfer from lactose to acceptor alcohols (R)-(-)-butan-2-ol, (RS)-butan-2-ol, (S)-(+)-propane-1,2-diol, (RS)-propane-1,2-diol, (S)-(+)-butane-1,3-diol, (RS)-butane-1,3-diol, propane-1,3-diol, (S)-(+)-isopropylideneglycerol (1,2-O-isopropylidene-sn-glycerol) and (RS)-isopropylideneglycerol (rac-1,2-O-isopropylideneglycerol) was studied, catalysed by the beta-galactosidase (beta-D-galactoside galactohydrolase EC 3.2.1.23) of Escherichia coli.Preference for galactosyl transfer to the R-enantiomers of chiral alcohols was observed, although selectivity was not pronounced.Higher selectivity for transfer to the primary hydroxy groups of the primary-secondary diols was observed.The results are interpreted in terms of a proposed active site model for the enzyme.
One of the oldest and most widely used commercial enzyme inhibitors is aspirin, Application of 24621-61-2, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 24621-61-2
Reference：
Synthesis and Crystal Structure of a Chiral C3-Symmetric Oxygen Tripodal Ligand and Its Applications to Asymmetric Catalysis,
Chiral lanthanide(III) complexes of sulphur–nitrogen–oxygen ligand derived from aminothiourea and sodium D-camphor-β-sulfonate