1-Phenyl-3-(2,4,6-trimethoxy­phen­yl)prop-2-en-1-one

In the title compound, C18H18O4, the dihedral angle between the mean planes of the aromatic rings is 7.39 (6)°. The dihedral angles between the linking C—C=C—C plane and the phenyl and benzene rings are 11.27 (5) and 4.20 (5)°, respectively

catena-Poly[[aqua­(2,2′-bipyridyl)cobalt(II)]-μ-5-nitro­isophthalato]

In the crystal structure of the title compound, [Co(C8H3NO6)(C10H8N2)(H2O)]n, there are two symmetry-independent one-dimensional coordination polymers, which are approximately related by noncrystallographic inversion symmetry. Each zigzag chain is constructed from one CoII ion, one O-monodentate 5-nitro­isophthalate (ndc) dianion, one N,N′-bidentate 2,2′-bipyridyl ligand and one water mol­ecule. A symmetry-generated O,O′-bidentate ndc dianion completes the cobalt coordination environment, which could be described as very distorted cis-CoN2O4 octa­hedral. The bridging ndc ligands result in parallel chains running along the a direction, and O—H⋯O hydrogen bonds arising from the water mol­ecules complete the structure

Dibutyl 5-[(4-ethoxycarbonylphenyl)diazenyl]benzene-1,3-dicarboxylate

In the title compound, C25H30N2O6, the dihedral angle between the aromatic rings is 3.79 (1) Å and the N=N bond shows a trans conformation. Both butyl side chains show evidence of disorder

Bis[2,4-penta­nedionato(1−)]bis­[4,4,5,5-tetra­methyl­-2-(4-pyrid­yl)-imidazoline-1-oxyl 3-oxide]manganese(II)

In the title compound, [Mn(C5H7O2)2(C12H16N3O2)], the manganese(II) cation (site symmetry ) is hexa­coordinated by four O and two N atoms in a distorted trans-MnN2O4 octa­hedral geometry. The four O atoms belonging to two 2,4-penta­nedionate anions lie in the equatorial plane and the two N atoms occupy the axial coordination sites

Bis(pentane-2,4-dionato-κ2 O,O′)bis­[4,4,5,5-tetra­methyl-2-(4-pyridyl)­imidazoline-1-oxyl 3-oxide-κN 2]manganese(II)

The title compound, [Mn(C5H7O2)2(C12H16N3O2)2], is isostructural with its NiII-containing analogue [Hao, Mu & Kong (2008 ▶). Acta Cryst. E64, m957]. The asymmetric unit comprises one-half of the mol­ecule and the MnII ion is located on an inversion centre. The coordination geometry around the MnII ion is slightly distorted octa­hedral, comprised of four O and two N atoms, in which the four O atoms in the equatorial plane come from two pentane-2,4-dionate ligands and the two N atoms in the axial coordination sites from 4,4,5,5-tetra­methyl-2-(4-pyrid­yl)imidazoline-1-oxyl 3-oxide

Triaqua­(2,2′-bipyridine)(5-nitro­isophthal­ato-κO)nickel(II) monohydrate

In the title compound, [Ni(C8H3NO6)(C10H8N2)(H2O)3]·H2O, the NiII cation is six-coordinated by a chelating 2,2′-bipyridine ligand, one carboxyl­ate O atom from a 5-nitro­isophthalate dianion and three water mol­ecules, with a slightly distorted cis-NiN2O4 octa­hedral geometry. The neutral complex is isolated, in contrast to coordination polymers formed by MnII, CoII and CuII with the same ligand set, but forms an extensive network of O—H⋯O hydrogen bonds between the coordinated and uncoordinated water mol­ecules and carboxyl­ate groups of the 5-nitro­isophthalate ions

Direct and Indirect Recycling Strategies of Expired Oxytetracycline for the Anode Material in Lithium Ion Batteries

It is well-known that the antibiotics inhibit the wide spread of various infection diseases and guarantee the life safety of many patients. However, various waste antibiotics into the environment also pose the great challenges of the environmental contamination and the ecological poison. Unreasonable disposal of expired antibiotics is one of the main sources of waste antibiotics in the ecological environment. For this reason, in order to focus on the circular economy of such highly refined medical grade chemicals, expired oxytetracycline was recycled for the anode active material in lithium ion batteries (LIBs) by direct and indirect strategies. That is, it was directly used as the anode active material or recycled by two-step carbonization for LIBs anode. Furthermore, the effect of these two strategies on the electrochemical performances was also discussed. Both anode materials showed their individual advantages and high feasibility for LIBs anode. For example, both them delivered the satisfactory Li-storage performances. Additionally, the direct route possessed lower recycling cost and high recovery rate, while the application range of carbon material in the indirect route was broader

Original Article Triptolide induces anti-inflammatory cellular responses

Abstract: Tripterygium wilfordii Hook F. has been used for centuries in traditional Chinese medicine to treat rheumatoid arthritis, an autoimmune disease associated with increased production of the pro-inflammatory cytokine, tumor necrosis factor (TNF)-α. Triptolide is a compound originally purified from T. wilfordii Hook F. and has potent anti-inflammatory and immunosuppressant activities. In this study, we investigated the effect of triptolide on the global gene expression patterns of macrophages treated with lipopolysaccharide (LPS). We found that LPS stimulation resulted in >5-fold increase in expression of 117 genes, and triptolide caused a >50% inhibition in 47 of the LPS-inducible 117 genes. A large portion of the genes that were strongly induced by LPS and significantly inhibited by triptolide were pro-inflammatory cytokine and chemokine genes, including TNF-α, IL-1β, and IL-6. Interestingly, LPS also induced the expression of micro-RNA-155 (miR-155) precursor, BIC, which was inhibited by triptolide. Confirming the cDNA array results, we demonstrated that triptolide blocked the induction of these pro-inflammatory cytokines as well as miR-155 in a dose-dependent manner. Profound inhibition of pro-inflammatory cytokine expression was observed at concentrations as low as 10-50 nM. However, triptolide neither inhibited the phosphorylation or degradation of IBα after LPS stimulation, nor affected the DNAbinding activity of NF-B. Surprisingly, we found that triptolide not only inhibited NF-B-regulated reporter transcription, but also dramatically blocked the activity of other transcription factors. Our study offers a plausible explanation of the therapeutic mechanism of T. wilfordii Hook F

The E3 Ubiquitin Ligase SCF(Cyclin F) Transmits AKT Signaling to the Cell-Cycle Machinery

The oncogenic AKT kinase is a key regulator of apoptosis, cell growth, and cell-cycle progression. Despite its important role in proliferation, it remains largely unknown how AKT is mechanistically linked to the cell cycle. We show here that cyclin F, a substrate receptor F-box protein for the SCF (Skp1/Cul1/F-box) family of E3 ubiquitin ligases, is a bona fide AKT substrate. Cyclin F expression oscillates throughout the cell cycle, a rare feature among the 69 human F-box proteins, and all of its known substrates are involved in proliferation. AKT phosphorylation of cyclin F enhances its stability and promotes assembly into productive E3 ligase complexes. Importantly, expression of mutant versions of cyclin F that cannot be phosphorylated by AKT impair cell-cycle entry. Our data suggest that cyclin F transmits mitogen signaling through AKT to the core cell-cycle machinery. This discovery has potential implications for proliferative control in malignancies where AKT is activated