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Necroptosis is a form of regulated cell death that has been implicated in multiple diseases. TNF-induced necroptosis is regulated by necrosomes, complexes consisting of RIPK1, RIPK3 and MLKL. In this study, by screening of a small-compound library, we identified dozens of compounds that inhibited TNF-induced necroptosis. According to the mechanisms by which they inhibited necroptosis, these compounds were classified into different groups. We then identified Ibrutinib as an inhibitor of RIPK3 and found that Quizartinib protected against the TNF-induced systemic inflammatory response syndrome in mice by inhibiting the activation of RIPK1. Altogether, our work revealed dozens of necroptosis inhibitors, suggesting new potential approaches for treating necroptosis-related diseases. Screening a library of compounds identifies several inhibitors of TNF-induced necroptosis, including Ibrutinib as an inhibitor of RIPK3 and Quizartinib as an indirect RIPK1 kinase activity inhibitor. [ABSTRACT FROM AUTHOR]

Niobic acid (Nb2O5·nH2O) was immobilized on regenerated cellulose (Re-Cellulose) to afford a heterogeneous catalyst, termed Nb2O5·nH2O@Re-Cellulose, that was characterized by powder X-ray diffraction, microscopy (SEM and TEM) and spectroscopic (Raman and FTIR) techniques. The surface acidity of the catalyst was determined using FTIR spectroscopy employing pyridine as a molecular probe. The Nb2O5·nH2O@Re-Cellulose catalyst was investigated in the conversion of glucose into 5-hydroxymethylfurfural (HMF) in aqueous media. The catalyst can be reused several times without undergoing a significant loss in activity. [ABSTRACT FROM AUTHOR]

A bi-functional cobalt and nitrogen co-doped carbon catalyst was fabricated by calcinating the chelate compound containing citric acid, melamine and CoCl2·6H2O in N2, with the mixed salts of LiCl and KCl as the template. Co and N species are highly dispersed in the target catalyst, which has a high surface area of 1011 m2 g−1. Such structure enables it to efficiently catalyze the direct aerobic oxidative esterification of benzyl alcohol with methanol to the ester of methyl benzoate; meanwhile, it exhibits superior potential ability for the application of oxygen reduction reaction, which is a vital process happening on the cathode of fuel cells and metal-air batteries. [ABSTRACT FROM AUTHOR]

A cadmium(ii)-based MOF, Cd-MDIP, was successfully prepared by hydrothermal reaction between the tetra-carboxylic ligand 5,5′-methylenebisophthalic acid (H4MDIP) and cadmium perchlorate. The X-ray crystal structure analysis showed that there are two uncoordinated carboxyl groups in each ligand and a 1D elliptical channel along the [001] direction. Because of the existence of uncoordinated carboxyl groups within open frameworks, Cd-MDIP exhibited a high sensitivity (Stern–Volmer constant KSV = 4.13 × 104 L mol−1) and a low detection limit (80 nM) for Fe3+ ions in pure water, which is much lower than the national standard for Fe3+ in daily drinking water (5.4 μM) set by the Ministry of Environmental Protection of P. R. China. Most importantly, Cd-MDIP also featured the ultrahigh adsorption of Fe3+ in aqueous solution that cannot be destroyed even by EDTA/base. Importantly, the MOF material (Cd-MDIP⊃Fe3+) after adsorbing Fe3+ could act as the first example of an excellent bi-metallic Lewis-acid catalyst for the cyanosilylation reaction of aromatic aldehydes in a size-selective fashion, and its efficiency was almost 10-times higher than that of the original Cd-MDIP. [ABSTRACT FROM AUTHOR]