Application of 7521-41-7, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 7521-41-7, Name is 2-Aminonicotinaldehyde, SMILES is O=CC1=CC=CN=C1N, belongs to pyridine-derivatives compound. In a article, author is Kodrin, Ivan, introduce new discover of the category.
Exploring and predicting intermolecular binding preferences in crystalline Cu(ii) coordination complexes
A simple model focusing on electrostatic contributions to interaction energies was found to be very effective for rationalizing the appearance of specific supramolecular interactions in a series of Cu(ii) coordination compounds. The experimental space was provided by a combination of Cu(ii) cations with acac-based anions (hexafluoracetylacetonato and trifluoracetylacetonato) and a series of pyridine-oxime ligands (3-pyridinealdoxime, methyl 3-pyridyl ketoxime, 4-pyridinealdoxime, methyl 4-pyridyl ketoxime, phenyl 4-pyridyl ketoxime). The calculated molecular electrostatic potential (MEP) values at competing hydrogen-bond acceptor sites, for ten structurally characterized complexes, provided guidelines for predicting supramolecular connectivity in cases when the MEP difference exceeded certain cut-off values, while two different and well-defined outcomes are possible within the so called ‘grey zone’, delineated by a range of MEP differences. It was also shown that the structural outcome within this region is determined by the influence of relatively weak, but distinct, auxillary interactions.
Application of 7521-41-7, One of the oldest and most widely used commercial enzyme inhibitors is aspirin, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 7521-41-7.
Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem