Search Results (2,129)

Background/Objectives: Acute lung injury (ALI) is a respiratory disorder lacking specific targeted therapy. Our preliminary screening revealed that the ethanol extract of the seeds of Podocarpus nakaii (EESPN) alleviated the symptoms of ALI in mice. The objectives of this study were to identify the active constituents in EESPN and study the mechanism involved. Methods: Column chromatography was performed to separate the chemical constituents of EESPN. The structures of the isolates were determined via spectroscopic methods. MTT assays, Western blotting, histological analysis, TUNEL assays, immunofluorescence staining, transcriptomic analysis, and quantitative real-time polymerase chain reaction (qRT–PCR) were employed to evaluate the anti-inflammatory activity and to elucidate the potential mechanism of nagilactone C (3, Nag C) in ALI treatment. Results: Twelve compounds were isolated from EESPN and structurally characterized. The structure of podolactone E (1) was confirmed via single-crystal X-ray diffraction. In vitro, Nag C showed potent anti-inflammatory activity in LPS-induced RAW 264.7 cells. Nag C liposomes significantly ameliorated LPS-induced histopathological damage to the lungs, reduced neutrophil infiltration and inflammatory cytokine levels, increased myeloperoxidase (MPO) activity, and promoted apoptosis in mice. In addition to suppressing inflammation, Nag C also significantly suppressed the phosphorylation of the NF-κB, STAT3, and STAT1 proteins. Conclusions: Nag C is an active constituent of EESPN. It may protect against LPS-induced ALI via inhibition of the STAT signaling pathway. Thus, Nag C is a promising lead compound in the development of novel STAT-targeted anti-inflammatory agents. Full article

(±)-tiaprofenic acid (TA), marketed as (Surgam^®), belongs to the family of NSAIDs, with the peculiarity of a reduced incidence of ulcer induction in rats compared with parent drugs. However, some adverse effects were observed, and better knowledge of its interaction with biologic substrates is needed. Unfortunately, unlike most commercial NSAIDs, suitable single crystals for an X-ray diffraction study could not be obtained. To fill the gap, the crystal structure of TA was solved by X-ray powder diffraction, and the molecular interactions stabilizing the structure were analyzed by Hirshfeld surface and energy framework analysis. TA crystallizes in the $P{2}_1/c$ space group, with its two enantiomers in the asymmetric unit, further confirming the peculiarity of the crystal structure and the difficulty of solving it. TA packing is characterized by alternating enantiomers connected through hydrogen bonds, forming chains, arranged in layers, stabilized by $\pi$-stacking. First principle modeling revealed several stable conformations within 4 $\mathrm{k}$$\mathrm{J}$/$\mathrm{mol}$ of the global minimum and the relaxed potential energy scans revealed modest (8 $\mathrm{k}$$\mathrm{J}$/$\mathrm{mol}$–15 $\mathrm{k}$$\mathrm{J}$/$\mathrm{mol}$) energy barriers. Such flat energy landscape suggests flexible and dynamic behavior of tiaprofenic acid in solution and in vivo conditions, with multiple suitable docking sites. Full article

Background: Bispecific antibodies have emerged as a promising class of therapeutics, enabling simultaneous targeting of two distinct antigens. Single-domain antibodies (sdAbs) comprising camelid variable heavy chains (VHHs) provide a compact and adaptable platform for bispecific antibody design due to their small size and ease of linkage. Methods: Here we investigate structure-activity relationship of VHH-based cytokine surrogates by combining cell signaling and functional assays with x-ray crystallography and other biophysical techniques. Results: We describe crystal structures of four unique bispecific VHHs that engage and activate the cytokine receptor pairs IL-18Rα/IL-18Rβ and IL-2Rβ/IL-2Rγ. These bispecific VHH molecules, referred to as surrogate cytokine agonists (SCAs), create unique cytokine signals that can be tuned by linker engineering. Our structural analysis reveals multiple dimeric conformations for these bispecific SCAs, where the two VHH domains can interact to form a compact structure. We demonstrate that the dimeric conformation can be enforced via engineering of a non-native disulfide bond between the VHH subunits, thus enhancing molecular thermostability. Conclusion: Our findings have important implications for the design and engineering of bispecific VHHs or sdAbs, offering a novel strategy for tuning their activity and increasing their stability. Full article

Fly ash, as the main solid waste of coal-fired power plants, is an environmental problem that needs to be solved due to its massive accumulation. The mechanical properties and optimization mechanism of lightweight aggregate concrete prepared by using new single-cylinder rotary kiln fly ash ceramic granules as aggregate were systematically investigated. Through orthogonal experimental design, combined with macro-mechanical testing and microscopic characterization techniques, the effects of cement admixture and ceramic granule admixture on the properties of concrete, such as compressive strength, split tensile strength, and modulus of elasticity, were analyzed, and the optimization scheme of key parameters was proposed. The results show that the new single rotary kiln fly ash ceramic particles significantly improve the mechanical properties of concrete by optimizing the porosity (water absorption ≤ 5%), and its 28-day compressive strength reaches 46~50.9 MPa, which is 53.3~69.7% higher than that of the ordinary ceramic concrete, and the apparent density is ≤1900 kg/m³, showing lightweight and high-strength characteristics. X-ray diffraction (XRD) analysis shows that the new ceramic grains form a more uniform, dense structure through the synergistic effect of internal mullite crystals and dense glass phase; computed tomography (CT) scanning shows that the total volume rate of cracks of the new ceramic concrete was reduced by up to 63.8% compared with that of ordinary ceramic concrete. This study provides technical support for the utilization of fly ash resources, and the prepared vitrified concrete meets the demand of green building while reducing structural deadweight (20~30%), which has significant environmental and economic benefits. Full article

Single crystals of the layered EuRECuTe₃ series with RE = Nd, Sm, Tb and Dy are obtained for the first time, completing the series of studies on quaternary tellurides synthesized using the halide flux method. These compounds crystallize in the orthorhombic space group Pnma (no. 62) with unit cell parameters ranging from a = 11.5634(7) Å, b = 4.3792(3) Å and c = 14.3781(9) Å for EuNdCuTe₃ to a = 11.2695(7) Å, b = 4.3178(3) Å and c = 14.3304(9) Å for EuDyCuTe₃. The influence of prismatic polyhedra [EuTe₆₊₁]⁷⁻ structural units on the stabilization of 3d framework composed by 2d layered fragments [RECuTe₃]²⁻, which have a key role in the interlayer interaction, is established. A comparative analysis of structural and magnetic properties dependence on the rare-earth element radius r_i(RE³⁺) in the EuRECuTe₃ series (RE = Sc, Y, Nd–Lu) is carried out. The structural contraction, including decrease in degree of tetrahedral polyhedra distortion, bond lengths shortening and unit cell volume shrinking with increasing r_i(RE³⁺), is established. It is shown that the structural alternation leads to transition from ferromagnetic to ferrimagnetic ordering. It was established that changes in the cationic sublattice have a more significant impact on structural transitions in the series of quaternary tellurides than changes in the anionic sublattice. The electronic structure and elastic and dynamic properties were estimated using ab initio calculations. The exfoliation energy for each compound is obtained by estimation of monolayer ground state energy as a result of structure relaxation. The symmetry and structural properties of monolayer EuRECuTe₃ (RE = Nd, Sm, Tb, Dy) compound are established and the orthorhombic symmetry is obtained with layer group pm2_1b. Full article

Foodborne pathogenic biofilms pose significant challenges to food safety due to their enhanced resistance to conventional antimicrobial agents. In this study, we evaluated the synergistic antibiofilm activity of oregano essential oil (OEO) from Lippia graveolens and the lytic bacteriophage phiLLS against six foodborne bacteria. GC–MS analysis achieved a 100% identification ratio, revealing that OEO was mainly composed of carvacrol (58.9%), p-cymene (28.6%), γ-terpinene (2.9%), and caryophyllene (2.6%). The MIC and MBC of OEO were 1 and 2 mg/mL, respectively, for all strains except E. coli BALL1119 (MIC = 2 mg/mL). We assessed biofilm biomass by crystal violet (CV) staining and metabolic activity using the TTC assay under both individual and combined treatments, monitored 9-hour planktonic growth kinetics to calculate Bliss and HSA synergy indexes, and employed atomic force microscopy (AFM) to visualize nanoscale alterations in Staphylococcus aureus and Escherichia coli BALL1119 biofilms. Combined OEO (2 mg/mL) and phiLLS (MOI 1) treatments achieved significantly greater biofilm biomass reduction than single agents, notably yielding >70% inhibition of S. aureus biofilms (p < 0.05) and a Bliss synergy index of 10.8% in E. coli BALL1119 growth kinetics, whereas other strains were additive. In biofilm assays, S. aureus and Salmonella spp. showed the highest reductions in biomass (CV) (71.0% and 67.8%, ΔHSA = 27.0% and 17.4%; ΔBliss = 21.1% and 13.8%) and metabolic activity (TTC) (68.6% and 48.5%). AFM revealed that OEO alone smoothed the extracellular matrix (averaging a 35% reduction in roughness), whereas the combined treatment caused fracturing (≈68 nm roughness) and prominent lytic pits. Although variability in S. aureus biofilm architecture precluded statistically significant pairwise comparisons, AFM topography and consistent trends in Ra/Rz parameters provided clear visual corroboration of the significant reductions detected by CV and TTC assays. These complementary data indicate that OEO primes the biofilm matrix for enhanced phage-mediated collapse, offering a green, two-step strategy for controlling resilient foodborne biofilms. Full article

Human methyltransferase-like protein 16 (METTL16) installs N⁶-methyladenosine on U6 small nuclear RNA (snRNA) and other RNAs. Multiple X-ray crystal structures of METTL16 have been published; however, we do not yet fully understand the structure–function relationships of specific residues. We designed 38 mutants, including seven cancer-associated mutants, and used electrophoretic mobility shift assays and single-turnover kinetic assays to better understand the functional roles of specific domains and amino acid residues in binding to U6 snRNA, formation of the METTL16•U6 snRNA•S-adenosylmethionine (SAM) complex, and the rate of methylation. While point mutations in the methyltransferase domain mildly weaken the binding of METTL16 to U6 snRNA, the C-terminal vertebrate conserved regions (VCRs), particularly the arginine-rich region (R382 to R388), mediate cooperative binding and contribute more to RNA binding. All METTL16 K-loop mutants displayed tighter SAM binding, suggesting that the K-loop blocks SAM binding. In addition, residues E133 and F227 are critical for stabilizing SAM binding. Mutations in the ₁₈₄NPPF₁₈₇ catalytic core and R282A abolished methyltransferase activity. Two METTL16 somatic cancer-associated mutants (G110C and R241Dfs*2) displayed reduced methylation activity. This mutational analysis expands our understanding of how specific domains and residues contribute to substrate-binding activity and methylation of U6 snRNA catalyzed by METTL16. Full article

This study focuses on developing and implementing crystal plasticity finite element modeling (CPFEM) codes on the ANSYS platform. The code incorporates a plasticity constitutive law that describes the behaviors of basal, prismatic, and pyramidal slips in magnesium, and is validated against plane-strain compression experiments and simulations using established codes on the ABAQUS CAE platform. The validated CPFEM code is applied to simulate the dislocation-induced nanoindentation response of pure magnesium across different crystallographic orientations, allowing visualization of strain distributions associated with different slips. Consistent with experimental observations, basal slip is identified as the primary active slip, whereas prismatic and pyramidal slips show varying activities with respect to the direction of the indentation. Novelty arises from an ANSYS–native CPFEM implementation that is cross-validated against published ABAQUS simulations and an experiment under a single, consistent constitutive set. This framework enables orientation-resolved mapping of slip system activity and subsurface strain fields under spherical nanoindentation, providing analysis capability seldom available in prior ANSYS–based studies. Full article

The present work reports a comparative study of thiosemicarbazone (H₂L¹) and dithiocarbazate (H₂L²) ligands and their Ni(II) complexes; [Ni(L¹)(PPh₃)] (1); [Ni(L¹)(Py)] (2); [Ni(L²)(PPh₃)] (3); and [Ni(L²)(Py)] (4). All compounds were characterized by spectroscopy analysis; and the complexes were also characterized by single-crystal X-ray diffraction. The crystal structures of the complexes revealed a distorted square planar geometry with the Ni(II) atoms coordinated to a double-deprotonated and tridentate ligand molecule by the ONS donor system. The coordination sphere is completed by the incorporation of pyridine or triphenylphosphine coligands at the metal center. Biological assays were conducted against the cell lines breast cancer (MCF-7); cisplatin-resistant ovarian cancer (A2780cis); lung cancer (A549); and nontumoral lung (MRC-5). The results show that cytotoxicity was significantly enhanced upon complexation for complexes (2) and (4); whereas it was suppressed for complexes (1) and (3) against the A2780cis and A549 cell lines. Notably; complex (2) exhibited superior cytotoxicity compared to cisplatin against both MCF-7 and A2780cis. Full article

Pyridinecarbonitriles (pyCN), also referred to as cyanopyridines, are promising ligands for the formation of pyridine-based coordination compounds due to their two different N-donor atoms, which enable versatile coordination modes. Copper(II) complexes containing pyCN derivatives are of particular interest for their potential applications in medicinal chemistry and materials science. In this study, the synthesis, structural characterization, and thermal and magnetic properties of three new copper(II) complexes with 3-pyCN, 4-pyCN, and ethyl picolinimidate, obtained in situ by means of alcoholysis of 2-pyCN, are reported: [Cu₂(μ-Ac)₄(3-pyCN)₂] (1), [Cu(H₂O)₂(Etpic)₂]NO₃ (2), and [Cu(NO₃)₂(CH₃CN)(4-pyCN)₂]·CH₃CN (3). Single-crystal X-ray diffraction confirmed that complex 1 features a dinuclear paddle-wheel structure with bridging acetato ligands and monodentate 3-pyCN molecules, coordinated through the ring nitrogen, while complexes 2 and 3 are mononuclear. Thermal analysis showed an intense and highly exothermic decomposition of complex 3, containing nitrate ligands. Magnetic measurements revealed strong antiferromagnetic coupling in the dinuclear complex 1, whereas complexes 2 and 3 displayed paramagnetic behavior with effective magnetic moments ranging from 1.8 μ_B to 2.0 μ_B, consistent with isolated Cu(II) centers. Full article

Lanthanide hydrogen-bonded organic frameworks (Ln-HOFs) integrating luminescent and proton-conductive properties hold significant promise for multifunctional sensing and energy applications, yet their development remains challenging due to the difficulty of balancing structural stability and functional diversity. In this context, this study successfully synthesized a novel neodymium(III)-based hydrogen-bonded framework material, formulated as {Nd(H₂O)₃(4-CPCA)[H(4-CPCA)]∙H₂O}ₙ (SNUT-15), via hydrothermal assembly using 1-(4-carboxyphenyl)-4-oxo-1,4-dihydropyridazine-3-carboxylic acid (H₂(4-CPCA)) as the ligand. Single-crystal X-ray diffraction analysis revealed a rare two-dimensional hydrogen-bonded bilayer structure stabilized by π-π stacking interactions and intermolecular hydrogen bonds. Hirshfeld surface analysis further corroborated the structural characteristics of this material. Moreover, leveraging the superior luminescent properties of lanthanide elements, this crystalline material exhibits dual functionality: selective fluorescence quenching toward Fe³⁺, La³⁺, and Mn²⁺ (with detection limits of 1.74 × 10⁻⁴, 1.88 × 10⁻⁴, and 3.57 × 10⁻⁴ mol·L⁻¹, respectively), as well as excellent proton conductivity reaching 7.92 × 10⁻³ S cm⁻¹ under conditions of 98% relative humidity and 353 K (80 °C). As a multifunctional neodymium(III)-based HOF material, SNUT-15 demonstrates its potential for applications in environmental monitoring and solid-state electrolytes, providing valuable insights into the rational design of lanthanide-containing frameworks. Full article

Background: Breast cancer continues to pose a significant global health challenge despite advances in early detection and targeted therapies. The development of novel chemotherapeutic agents remains crucial, particularly those with selective cytotoxicity toward specific breast cancer subtypes. Methods: A series of ten hybrid indolyl-methylidene phenylsulfonylhydrazones and one bis-indole derivative were designed, synthesized, and structurally characterized using NMR and high-resolution mass spectrometry (HRMS). Prior to synthesis, in silico screening was performed to assess drug likeness and ADME-related properties. Single-crystal X-ray diffraction was conducted for compound 3e. The cytotoxic potential of the synthesized compounds was evaluated using the MTT assay against MCF-7 (ER-α⁺) and MDA-MB-231 (triple-negative) breast cancer cell lines. Additionally, quantitative structure–activity relationship (QSAR) analysis was conducted to identify key structural features contributing to activity. Results: Most compounds exhibited selective cytotoxicity against MCF-7 cells. Notably, compound 3b demonstrated the highest potency with an IC₅₀ of 4.0 μM and a selectivity index (SI) of 20.975. Compound 3f showed strong activity against MDA-MB-231 cells (IC₅₀ = 4.7 μM). QSAR analysis revealed that the presence of a non-substituted phenyl ring and specific indolyl substituents (5-methoxy, 1-acetyl, 5-chloro) significantly contributed to enhanced cytotoxic activity and ligand efficiency. Conclusion: The synthesized phenylsulfonylhydrazone hybrids exhibit promising and selective cytotoxicity, particularly against ER-α⁺ breast cancer cells. Structural insights from QSAR analysis provide a valuable foundation for the further optimization of this scaffold as a potential source of selective anticancer agents. Full article

The microcrack initiation and evolution behavior of Fe-C alloy under uniaxial tensile loading are investigated using molecular dynamics (MD) simulations. The model is stretched along the z-axis at a strain rate of 2 × 10⁹ s⁻¹ and temperatures ranging from 300 to 1100 K, aiming to elucidate the microscopic deformation mechanisms during crack evolution under varying thermal conditions. The results indicate that the yield strength of Fe-C alloy decreases with a rising temperature, accompanied by a 25.2% reduction in peak stress. Within the temperature range of 300–700 K, stress–strain curves exhibit a dual-peak trend: the first peak arises from stress-induced transformations in the internal crystal structure, while the second peak corresponds to void nucleation and growth. At 900–1100 K, stress curves display a single-peak pattern, followed by rapid stress decline due to accelerated void coalescence. Structural evolution analysis reveals sequential phase transitions: initial BCC-to-FCC and -HCP transformations occur during deformation, followed by reversion to BCC and unidentified structures post-crack formation. Elevated temperatures enhance atomic mobility, increasing the proportion of disordered/unknown structures and accelerating material failure. Higher temperatures promote faster potential energy equilibration, primarily through accelerated void growth, which drives rapid energy dissipation. Full article

Coordination polymer [{Co(tta)₂(4,4′-bipy)}_n] (1) (tta = 4,4,4 trifluoro-1-(2-thienyl)-1,3-butanedionate; 4,4′-bipy = 4,4′-bipyridine) was synthesized by reacting [Co(tta)₂-(H₂O)₂] with equivalent of 4,4′-bipy, whereby the aqua ligands in [Co(tta)₂-(H₂O)₂] were replaced by 4,4′-bipy ligand. Thermal behavior, investigated via thermogravimetric analysis (TGA), revealed that 1 decomposes between 290 and 400 °C. The solid-state structure of 1 was confirmed by single-crystal X-ray diffraction, which established its polymeric nature of 1. Each monomer unit of 1 features a cobalt center in an octahedral coordination environment, with two equatorially chelating tta ligands and one axially oriented 4,4′-bipy ligand. Sulfur–sulfur interactions lead to the formation of a two-dimensional supramolecular network. In addition, compound 1 is stabilized by various intermolecular interactions, including C-H···π, C-F···F-C, and C-H···F-C contacts. Hirshfeld surface analysis and 2D-fingerprint plots were employed to further investigate the non-covalent intermolecular interactions in the solid state, providing strong evidence for their role in stabilizing the crystal structure. Full article

The reaction of rhodanine vinyl bithiophene (BTR) with molecular dibromine (Br₂) resulted in the formation of compound 1. Single-crystal X-ray diffraction analysis revealed bromination of the terminal thiophenyl ring and the formation of a 1:1 CT “spoke” adduct between the rhodanine thiocarbonyl group and a neutral dibromine (Br₂) molecule. Full article