Zur Kenntnis der μ-Peroxo-bis(pentacyanokobaltate(III)). Neuartige Darstellung,Beschreibung eines μ-Hydroperoxo-komplexes K5[Co2OOH(CN)10] · 2 H2O und eines μ-Peroxo-Carbonato-Komplexes K6[Co2CO4(CN)10] · 2 H2O

Investigations on Metal Catalysts. XXII. Chemisorption of Hydrogen on Pt? Ru and η-Al₂O₃ Supported Pt? Ru Catalysts Measurements of the H₂ chemisorption by volumetric method were carried out on several series of Pt? Ru and η-Al₂O₃ supported Pt? Ru catalysts. Addition of Ru to Pt and vice versa effects a remarkable influence on the sorption behaviour of the starting samples. For mixtures of carrier-free catalysts and η-Al₂O₃ as well as Pt? Ru/η-Al₂O₃ catalysts a hydrogen-spillover effect was found.     

LIOUVILLE RESULTS FOR STABLE SOLUTIONS OF QUASILINEAR EQUATIONS WITH WEIGHTS

This paper is devoted to the quasilinear equation ■where p 2,Ω is a(bounded or unbounded) domain of R~N,w_1,w_2 are nonnegative continuous functions and f is an increasing function. We establish a Liouville type theorem for nontrivial stable solutions of the equation under some mild assumptions on Ω,w_1, w_2 and f, which extends and unifies several results on this topic.     

A rapid way to synthesize Brønsted acidic ionic liquid and its application as an efficient catalyst for esterification

A novel and time-saving method to prepare a Brønsted acidic ionic liquid, 1-carboxymethyl-3-methylimidazolium hydrogen sulfate ([CMI][HSO₄]), in high yield and purity was performed under microwave irradiation. The ionic liquid showed an incomparable catalytic efficiency in the microwave-accelerated esterification of arenecarboxylic acids. Moreover, its ability of being recovered and reused many times without loss of activity has made [CMI][HSO₄] more favorable from the viewpoint of green chemistry.     

Analysis of trace elements in the fingernails of breast cancer patients using instrumental neutron activation analysis

Journal of Radioanalytical and Nuclear Chemistry - The aim of this study was to find trace elements that increase risk of breast cancer based on the deviation of the concentration of trace elements...     

Acylated flavonoid glycosides from Barringtonia racemosa

Abstract

Using various chromatographic separations, three new acylated flavonoid glycosides, namely barringosides G–I (1–3), were isolated from the water-soluble extract of Barringtonia racemosa branches and leaves. The structure elucidation was performed by extensive analysis of the 1D and 2D NMR and HR-QTOF-MS data. Of the isolated compounds, barringoside I (3) showed moderate inhibitory effects on LPS-induced NO production in RAW264.7 cells with an IC₅₀ of 52.48?±?1.04?µM.     

Target Design of Novel Histone Deacetylase 6 Selective Inhibitors with 2-Mercaptoquinazolinone as the Cap Moiety

Epigenetic alterations found in all human cancers are promising targets for anticancer therapy. In this sense, histone deacetylase inhibitors (HDACIs) are interesting anticancer agents that play an important role in the epigenetic regulation of cancer cells. Here, we report 15 novel hydroxamic acid-based histone deacetylase inhibitors with quinazolinone core structures. Five compounds exhibited antiproliferative activity with IC₅₀ values of 3.4–37.8 µM. Compound 8 with a 2-mercaptoquinazolinone cap moiety displayed the highest antiproliferative efficacy against MCF-7 cells. For the HDAC6 target selectivity study, compound 8 displayed an IC₅₀ value of 2.3 µM, which is 29.3 times higher than those of HDAC3, HDAC4, HDAC8, and HDAC11. Western blot assay proved that compound 8 strongly inhibited tubulin acetylation, a substrate of HDAC6. Compound 8 also displayed stronger inhibition activity against HDAC11 than the control drug Belinostat. The inhibitory mechanism of action of compound 8 on HDAC enzymes was then explored using molecular docking study. The data revealed a high binding affinity (−7.92 kcal/mol) of compound 8 toward HDAC6. In addition, dock pose analysis also proved that compound 8 might serve as a potent inhibitor of HDAC11.