catena-Poly[[[(1,10-phenanthroline)copper(I)]-μ-cyanido] ethanol hemisolvate]

In the title coordination polymer, {[Cu(CN)(C12H10N2)]·0.5C2H5OH}n, there are two CuI ions, two 1,10-phenanthroline (phen) ligands and two cyanide ions in the asymmetric unit along with a highly disordered ethanol solvent mol­ecule, which was modelled as being disordered over two sets of sites in a 0.829 (7):0.171 (7) ratio. The orientation/ordering of the C and N atoms of the cyanide ions could not be determined in the present refinement and they were modelled as being statistically disordered. Both copper ions are coordinated by an N,N′-bidentate phen ligand and two cyanide ligands, generating distorted tetra­hedral CuN2 Q 2 (Q = C or N) tetra­hedra. The μ-cyanide ligands link the metal ions, forming a zigzag chain propagating in [001]. The chains are cross-linked by numerous aromatic π–π stacking contacts between adjacent phen rings [minimum centroid–centroid separation = 3.620 (3) Å]

N-Benzyl­pyridin-2-amine

In the title compound, C12H12N2, the dihedral angle between the benzene and pyridine rings is 67.63 (8)°. Mol­ecules are linked into centrosymmetric dimers by a simple inter­molecular N—H⋯N hydrogen bond with graph-set motif R 2 2(8)

Bis[2-(1H-benzimidazol-2-yl)benzoato]copper(II) dihydrate

In the title compound, [Cu(C14H9N2O2)2]·2H2O, the Cu(II) ion lies on a centre of symmetry and is four-coordinated by two N atoms and two O atoms from two 2-(1H-benzimidazol-2-yl)benzoate ligands in a square-planar environment. The benzimidazol and benzyl rings form a dihedral angle of 42.8 (5)°. The mol­ecule contains two H-bonded carboxyl O acceptors and two H-bonded N—H donors in the benzimidazol groups, which inter­act with two symmetry-related uncoordinated water mol­ecules so that neighboring mol­ecular units are linked by (O—H)water⋯Ocarbox­yl hydrogen bonds with an R 2 4(8) graph-set motif, generating a helical chain in the a-axis direction. These chains are, in turn, inter­connected by (N—H)benzimidazol⋯Owater hydrogen bonds, forming a three-dimensional supra­molecular network

catena-Poly[tris­(μ2-1H-benzimidazole-5-carboxyl­ato)europium(III)]

In the title one-dimensional coordination polymer, [Eu(C8H5N2O2)3]n, the EuIII ion is eight-coordinated by the carboxyl­ate O atoms of six ligands in a distorted monocapped penta­gonal–bipyramidal geometry. The ligands link EuIII ions, forming helical chains parallel to the c axis, with Eu⋯Eu separations of 4.0678 (11) Å. The chains are further inter­connected by N—H⋯N hydrogen bonds into a three-dimensional supra­molecular network. The crystal studied was a racemic twin, as suggested by the Flack parameter of 0.367 (14)

Thioetherimide-Modified Cyanate Ester Resin with Better Molding Performance for Glass Fiber Reinforced Composites

Cyanate ester (CE) resins with higher heat resistance, lower coefficients of thermal expansion (CTEs), and lower water absorption ratios are highly desired in printed circuit boards (PCBs). In this work, a CE was modified by copolymerization with a long-chain thioether bismaleimide (SBMI) to form a thioetherimide-modified CE (SBT). The results indicated that SBT had a wider processing window and better processing properties than a common bismaleimide-modified CE resin (MBMI). After molding with a glass fiber cloth, the composites (GSBT) exhibited moisture adsorption in the range of 1.4%–2.0%, high tensile strength in the range of 311–439 MPa, good mechanical retention of 70%–85% even at 200 °C, and good dimension stability, with coefficients of thermal expansion in the range of 17.3–18.6 (×10−6 m/°C). Such GSBT composites with superior properties would be good candidates for PCB applications

Dimethylammonium 5-carboxy-2-(1-oxo-1λ5-pyridin-2-yl)-1H-imidazole-4-carboxylate

In the title salt, C2H8N+·C10H6N3O5−, the imidazolecarboxylate anion is essentially planar [maximum deviation from the least-squares plane = 0.046 (5) Å], with a dihedral angle between the rings of 2.7 (2)°. This conformation is maintained by the presence of both intramolecular carboxy–carboxylate O—H...O and imidazole–oxide N—H...O hydrogen bonds. Iin the crystal, cation–carboxylate N—H...O and cation–imidazole N—H...N hydrogen bonds result in chains along the b axis

<i>β</i>-Nicotinamide Mononucleotide Promotes Cell Proliferation and Hair Growth by Reducing Oxidative Stress

β-Nicotinamide mononucleotide (NMN) has shown promising effects on intestinal health, and it is extensively applied as an anti-aging and Alzheimer’s disease therapeutic, due to its medicinal properties. The effects of NMN on the growth of mouse hair were observed after hair removal. The results indicated that NMN can reverse the state of hair follicle atrophy, hair thinning, and hair sparsity induced by dihydrotestosterone (DHT), compared to that of minoxidil. In addition, the action mechanisms of NMN promoting hair growth in cultured human dermal papilla cells (HDPCs) treated with DHT were investigated in detail. The incubation of HDPCs with DHT led to a decrease in cell viability and the release of inflammatory mediators, including interleukin-6 (IL-6), interleukin-1Beta (IL-1β) and tumor necrosis factor Alpha (TNF-α). It was found that NMN can significantly lower the release of inflammatory factors induced by DHT in HDPCs. HDPCs cells are protected from oxidative stress damage by NMN, which inhibits the NF-κB p65 inflammatory signaling pathway. Moreover, the levels of androgen receptor (AR), dickkopf-1 (DKK-1), and β-catenin in the HDPCs were assessed using PCR, indicating that NMN can significantly enhance the expression of VEGF, reduced IL-6 levels and suppress the expression of AR and DKK-1, and notably increase β-catenin expression in DHT-induced HDPCs