Loganmccann3817

Moreover, it was found that compounds 15 and 19 could suppress the phosphorylation of IκBα and NF-κB/p65 to prevent it from shifting into the nucleus and downregulate the expression of inflammatory factors, such as iNOS, IL-6 and TNF-α. Our investigations revealed that the NO inhibitory effects of the active triterpenes obtained from Z. jujuba were mediated, at least in part, through the NF-κB signaling pathway.A system of micro-spheres immersed in a water-in-oil microemulsion (ME) is studied both theoretically and experimentally. this website A catalyst for the Belousov-Zhabotinsky (BZ) reaction is immobilized in the micro-spheres, which are called BZ micro-oscillators (BZ MOs). The ME is loaded with all the reagents of the BZ reaction, except the catalyst. Fresh BZ reagents in the ME constantly feed BZ MOs. Diffusively coupled BZ MOs in this system demonstrate excitatory coupling at short gaps and inhibitory coupling at long gaps between BZ MOs. The critical gap, at which the transition between excitatory and inhibitory types of coupling occurs, depends on both the BZ concentration and the size of the ME nanodroplets and can range from a few to tens of micrometers. Different oscillatory patterns of BZ MOs with in-phase and anti-phase oscillations of neighboring BZ MOs have been found. Turing patterns are found as well. A network of such BZ MOs can be used for the creation of a chemical computer.A one-pot catalytic method has been developed for the stereoselective synthesis of cyclopropane-fused cyclic amidines using CuBr2/K2S2O8 as an efficient single electron transfer (SET) oxidative system. The generality of this mild method is demonstrated with a wide variety of substrates to furnish pharmaceutically important amidines containing aza-bicyclic and novel aza-tricyclic frameworks in very good yields. A chemoselective reduction of cyclic amidines to 2-/3-azabicyclo[m.n.0]alkanes and octahydroindoles has been developed using a NaBH4/I2 reagent system. The synthetic scope of the chemoselective reduction of the amidine functionality has been exemplified in the stereoselective synthesis of an iminosugar based (±)-epiquinamide analogue.Nanoparticles (NPs) promise a huge potential for clinical diagnostic and therapeutic applications. However, nano-bio (e.g., the NP-cell membrane) interactions and underlying mechanisms are still largely elusive. In this study, two types of congeneric peptides, namely PGLa and magainin 2 (MAG2), with similar membrane activities were employed as model ligands for NP decoration, and the diffusion behaviours (including both translation and rotation) of the ligand-decorated NPs on a lipid bilayer membrane were studied via molecular dynamics simulations. It was found that, although both PGLa- and MAG2-coated NPs showed alternatively "hopping" and "jiggling" diffusions, the PGLa-coated ones had an enhanced circling at the hopping stage, while a much confined circling at the jiggling stage. In contrast, the MAG2-coated NPs demonstrated constant circling tendencies throughout the diffusion process. Such differences in the coupling between translational and rotational dynamics of these two types of NPs are ascribed to the different ligand-lipid interactions of PGLa and MAG2, in which the PGLa ligands prefer to vertically insert into the membrane, while MAG2 tends to lie flat on the membrane surface. Our results are helpful for the understanding the underlying associations between the NP motions and their interfacial membrane interactions, and shed light on the possibility of regulating NP behaviours on a cellular surface for better biomedical uses.Potassium-ion battery (KIB) is one of the emerging electrochemical energy storage technologies due to the abundance, low cost, and low redox potential of K. One of the most promising cathodes of KIBs is a layered vanadium-based compound, but it often suffers from fast capacity decay during repeated cycling. Herein, a K0.5V2O5/CNTs hybrid film composed of K0.5V2O5 nanobelt and carbon nanotube (CNT) network was synthesized by an electrostatic self-assembly and vacuum filtration process, and further used as the cathode in KIBs. The K0.5V2O5/CNTs cathode possessed a flexible and interconnected network structure, which not only offered fast kinetics for electron transfer and ion transportation, but also provided an elastic medium to buffer the large volume change of the K0.5V2O5 nanobelts during cycling. As a cathode for KIBs, the K0.5V2O5/CNTs electrode showed a reversible discharge capacity of ∼90 mA h g-1 at 50 mA g-1 and exhibited good cycling stability (88.8% capacity retention for 100 cycles at 50 mA g-1, 82.2% capacity retention for 300 cycles at 500 mA g-1) and excellent rate performance of ∼62 mA h g-1 at 500 mA g-1. K-Ion full battery testing further confirmed its good electrochemical performance by presenting a high reversible discharge capacity (68 mA h g-1 at 50 mA g-1) and long-term retention (>80% after 80 cycles). Interestingly, a cable-shaped KIB with the flexible K0.5V2O5/CNTs film as the cathode electrode was assembled and showed its further application potential as a power source for wearable electronics.Rational design of molecular chelating agents requires a detailed understanding of physicochemical ligand-metal interactions in solvent phase. Computational quantum chemistry methods should be able to provide this, but computational reports have shown poor accuracy when determining absolute binding constants for many chelating molecules. To understand why, we compare and benchmark static- and dynamics-based computational procedures for a range of monovalent and divalent cations binding to a conventional cryptand molecule 2.2.2-cryptand ([2.2.2]). The benchmarking comparison shows that dynamics simulations using standard OPLS-AA classical potentials can reasonably predict binding constants for monovalent cations, but these procedures fail for divalent cations. We also consider computationally efficient static procedure using Kohn-Sham density functional theory (DFT) and cluster-continuum modeling that accounts for local microsolvation and pH effects. This approach accurately predicts binding energies for monovalent and divalent cations with an average error of 3.