Synthetic Route of 6969-71-7, Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. 6969-71-7, Name is [1,2,4]Triazolo[4,3-a]pyridin-3(2H)-one, SMILES is O=C1NN=C2C=CC=CN21, belongs to pyridine-derivatives compound. In a article, author is Surov, Artem O., introduce new discover of the category.
Novel cocrystals of the potent 1,2,4-thiadiazole-based neuroprotector with carboxylic acids: virtual screening, crystal structures and solubility performance
Five new multicomponent solid forms of the biologically active 1,2,4-thiadiazole derivative (TDZH) with dicarboxylic and hydroxybenzoic acids have been discovered by combined virtual/experimental cocrystal screening. The interplay between the intrinsic hierarchy of the donor/acceptor groups in the TDZH/coformer molecules and the hydrogen bond pattern in the multicomponent crystals was rationalized using quantitative analysis of molecular electrostatic potential (MEP) surfaces along with periodic DFT computations. All the TDZH cocrystals are based on a carboxy-aminothiadiazole heterosynthon which is stabilized by a combination of enthalpic factors and the supramolecular chelating effect. According to the analysis of the non-covalent interaction energies, the mean energy value of this heterosynthon equals similar to 77 kJ mol(-1), which is comparable to the well-known carboxyl-amide and carboxyl-pyridine synthons in terms of the dissociation energy. The thermal stability of the multicomponent crystals was investigated by the DSC and TG methods. The pH-solubility behavior of the cocrystals was investigated at different pH values using eutectic concentrations of the components. Three out of five co-crystals were found to be more soluble than the parent TDZH at low pH values (approximate to 2.0). However, cocrystallization significantly alters the solubility-pH dependence of TDZH, increasing the compound solubility at neutral pH values.
Synthetic Route of 6969-71-7, Because enzymes can increase reaction rates by enormous factors and tend to be very specific, typically producing only a single product in quantitative yield, they are the focus of active research.you can also check out more blogs about 6969-71-7.
Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem