Microwave-assisted synthesis of a MK2 inhibitor by Suzuki-Miyaura coupling for study in Werner syndrome cells

Microwave-assisted Suzuki-Miyaura cross-coupling reactions have been employed towards the synthesis of three different MAPKAPK2 (MK2) inhibitors to study accelerated aging in Werner syndrome (WS) cells, including the cross-coupling of a 2-chloroquinoline with a 3-pyridinylboronic acid, the coupling of an aryl bromide with an indolylboronic acid and the reaction of a 3-amino-4-bromopyrazole with 4-carbamoylphenylboronic acid. In all of these processes, the Suzuki-Miyaura reaction was fast and relatively efficient using a palladium catalyst under microwave irradiation. The process was incorporated into a rapid 3-step microwave-assisted method for the synthesis of a MK2 inhibitor involving 3-aminopyrazole formation, pyrazole C-4 bromination using N-bromosuccinimide (NBS), and Suzuki-Miyaura cross-coupling of the pyrazolyl bromide with 4-carbamoylphenylboronic acid to give the target 4-arylpyrazole in 35% overall yield, suitable for study in WS cells

Microwave-assisted synthesis of a MK2 inhibitor by Suzuki-Miyaura coupling for study in Werner syndrome cells

Microwave-assisted Suzuki-Miyaura cross-coupling reactions have been employed towards the synthesis of three different MAPKAPK2 (MK2) inhibitors to study accelerated aging in Werner syndrome (WS) cells, including the cross-coupling of a 2-chloroquinoline with a 3-pyridinylboronic acid, the coupling of an aryl bromide with an indolylboronic acid and the reaction of a 3-amino-4-bromopyrazole with 4-carbamoylphenylboronic acid. In all of these processes, the Suzuki-Miyaura reaction was fast and relatively efficient using a palladium catalyst under microwave irradiation. The process was incorporated into a rapid 3-step microwave-assisted method for the synthesis of a MK2 inhibitor involving 3-aminopyrazole formation, pyrazole C-4 bromination using N-bromosuccinimide (NBS), and Suzuki-Miyaura cross-coupling of the pyrazolyl bromide with 4-carbamoylphenylboronic acid to give the target 4-arylpyrazole in 35% overall yield, suitable for study in WS cells

Differential expression of zinc transporters accompanies the differentiation of C2C12 myoblasts

Zinc transporters facilitate metal mobilization and compartmentalization, playing a key role in cellular development. Little is known about the mechanisms and pathways of Zn movement between Zn transporters and metalloproteins during myoblast differentiation. We analyzed the differential expression of ZIP and ZnT transporters during C2C12 myoblast differentiation. Zn transporters account for a transient decrease of intracellular Zn upon myogenesis induction followed by a gradual increase of Zn in myotubes. Considering the subcellular localization and function of each of the Zn transporters, our findings indicate that a fine regulation is necessary to maintain correct metal concentrations in the cytosol and subcellular compartments to avoid toxicity, maintain homeostasis, and for loading metalloproteins needed during myogenesis. This study advances our basic understanding of the complex Zn transport network during muscle differentiation

Molecular dynamics as a tool to study heterogeneity in zeolites - Effect of Na cations on diffusion of CO and N in Na-ZSM-5

Zeolites typically contain extra-framework cations to charge-compensate for trivalent Al atom substitutions in the SiO framework. These cations, such as Na, directly interact with quadrupolar guest molecules, such as CO and N, which move through their micropores, causing energetic heterogeneity. To assess the effects of heterogeneity in Na-ZSM-5 on diffusion of CO and N, molecular dynamics (MD) simulations are carried out. In silicalite-1, the pure-silicon form of ZSM-5, the self-diffusivity exhibits a monotonic decrease with molecular loading, while the corrected diffusivity shows a relatively constant value. In contrast, the Na cations cause a maximum or a flat profile over molecular loading for the self- and corrected diffusivities of CO at T=200 and 300K, while the cations only have minimal impact on the diffusivity of N. The MD simulations allow us to identify energy basins or sites at which guest molecules spend a relatively long time, and construct a coarse-grained lattice representation for the pore network. Average residence times at these sites are calculated for both species. The trends observed in the residence times correlate to the trends observed in the diffusivity. The residence times for CO at T=200K are long at low loading, but decrease with loading as additional CO molecules compete to stay close to a cation. In contrast, the residence times for N are relatively insensitive to the cations, only mildly increasing near a cation. This difference in behavior can be associated to the quadrupole moments of these molecules

Coulomb-assisted Σ−\bm\Sigma^--nucleus bound states in the (K−K^-, π+\pi^+) reaction

We study a production of Coulomb-assisted $\Sigma^-$-nucleus bound states by nuclear ($K^-$, $\pi^+$) reactions within a distorted-wave impulse approximation, so as to examine several types of the $\Sigma$-nucleus potentials that are consistent with the available $\Sigma^-$ atomic X-ray data and nuclear ($\pi^-$, $K^+$) data. We theoretically demonstrate the inclusive ($K^-$, $\pi^+$) spectra of the $\Sigma^-$ unstable bound states on $^{28}$Si, $^{58}$Ni, and $^{208}$Pb targets at incident $K^-$ lab momenta $p_{K}= 400\text{--}800$ MeV/c. The results show that the near-recoilless ($K^-$, $\pi^+$) reaction on the $^{58}$Ni target gives a clear candidate to confirm properties of the $\Sigma$-nucleus potentials having a repulsion inside the nuclear surface and an attraction outside the nucleus with a sizable absorption, whereas details of the repulsion of the potential at the nuclear center cannot be determined by the inclusive spectra. This is a promising attempt to extract properties of the $\Sigma$-nucleus potential in the nucleus at forthcoming J-PARC experiments, as a full complement to the analyses of the $\Sigma^-$ atomic and ($\pi^-$, $K^+$) data