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Inflammation is the body's response to defence against infection or injury, and is associated with the progression of many diseases, such as inflammatory bowel disease (IBD) and rheumatoid arthritis (RA). LCA, a dibenzylbutane lignan extracted from the roots of traditional medicinal plant (Lour.) Pers., has demonstrated promising anti-inflammatory activity. In this study, a series of novel LCA derivatives were designed, synthesized, and evaluated for anti-inflammatory activity. Lipopolysaccharide (LPS)-induced RAW 264.7 cell model experiments showed that compound 10h (at 20 μM of concentration) had the strongest inhibitory effect on NO release, and inhibited the secretion and gene expression levels of interleukin (IL)-1β, IL-6, and tumor necrosis factor (TNF)-α In addition, western blot, immunofluorescence, and molecular docking showed that the anti-inflammatory mechanism of compound 10h may be related to the nuclear factor (NF)-κB signalling pathway. studies based on a carrageenan-induced mouse paw edema model have shown significant anti-inflammatory activity of compound 10h at 20 mg kg. Preliminary and studies indicate that compound 10h has the potential to be developed as a novel anti-inflammatory agent.
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http://dx.doi.org/10.1039/d4md00053f | DOI Listing |
RSC Adv
August 2025
Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences Tehran Iran
In this study, novel 1,1'-hydrazine-bis(phenoxy-1,2,3-triazol-acetamide) derivatives 10a-n were synthesized, and because of their structural features, they were evaluated against acetylcholinesterase (AChE), butyrylcholinesterase (BChE), and α-glucosidase. AChE and BChE are two important targets in the treatment of Alzheimer's disease (AD), and α-glucosidase is a carbohydrate-hydrolyzing enzyme with therapeutic importance in diabetes. Furthermore, cell studies were performed on the title compounds against SH-SY5Y neuroblastoma cells as a cancer cell line and HEK293 cells as a normal cell line.
View Article and Find Full Text PDFFuture Med Chem
July 2025
Department of Chemistry, Faculty of Sciences, Kahramanmaras Sutcu Imam University, Kahramanmaras, Turkey.
This study aimed to synthesize novel nitrophenol-triazole hybrid molecules, investigate their biological activities (cholinesterase inhibition, antioxidant, and anticancer effects), and profile them using computational methods (molecular docking, ADMET). Eight new hybrid compounds were successfully synthesized, and the crystal structures of compounds were determined by single-crystal X-ray diffraction analysis. Among the obtained compounds, derivative exhibited notable cholinesterase inhibitory activity with high potency and selectivity against acetylcholinesterase (AChE), demonstrating an IC value of 1.
View Article and Find Full Text PDFFront Chem
July 2025
Engineering Research Center of Sports Health Intelligent Equipment of Hubei Province, Wuhan Sports University, Wuhan, China.
This paper provides a strategy for detecting and monitoring volatile organic compounds released from plastic runway tracks. The method applies a simultaneous determination of 101 VOCs based on the environmental chamber-canister sampling-three-stage cold trap preconcentration-gas chromatography-mass spectrometry/flame ionization detection (GC-MS/FID) method. For this purpose, an environmental chamber, SUMMA canisters, an atmospheric pre-concentrator, and a GC-MS/FID dual detection setup were adopted to collect VOCs released from plastic athletic tracks in an environmental chamber, followed by their preconcentration in a three-stage cold trap including glass-bead cold trap concentration, Tenax tube cold trap concentration, and capillary glass tube absorption focusing.
View Article and Find Full Text PDFMaterials (Basel)
June 2025
Chemistry Department, College of Science, Imam Abdulrahman Bin Faisal University, P.O. Box 76971, Dammam 31441, Saudi Arabia.
This study investigates the synthesis process and characterization methods and evaluates the inhibition behavior of olanzapine (2-methyl-4-(4-methyl-1-piperazinyl)-10H-thieno-[2,3-b] 1,5]benzodiazepine (OLZ)) and its derivatives, such as 3-(2-methyl-4-(4-methylpiperazin-1-yl)-10H-benzo[b]thieno[2,3-e] [1,4]diazepin-10-yl) propenamide (OLZ1) and Ethyl 2-(2-methyl-4-(4-methylpiperazin-1-yl)-10H-benzo[b]thieno[2,3-e][1,4]diazepin-10 yl) acetate (OLZ2) for carbon steel (C1018) in a 1 M HCl acidic solution. Fourier Transform Infrared Spectroscopy (FTIR) and Nuclear Magnetic Resonance (NMR) were employed to verify their molecular structures and functional groups, which characterized the derivatives after synthesis. Their corrosion inhibition potential for C1018 steel in acidic media was estimated by weight loss (WL) and electrochemical techniques, such as electrochemical impedance spectroscopy (EIS), linear polarization resistance (LPR), and potentiodynamic polarization (PDP), accompanied by surface analysis methods.
View Article and Find Full Text PDFInorg Chem
July 2025
Department of Chemistry, Georgetown University, Washington, D.C. 20057, United States.
The synthesis, structural characterization, and spectroscopic properties of five tetravalent uranium (U) phases including Li[U(μ-O)Cl(HO)]·10HO (), [U(HO)Cl] (), [U(HO)Cl]·KCl (), RbUCl (), and CsUCl () are reported. Notably, a change in the U solid-state structural unit was observed based on the identity of the alkali counterion used in the synthesis. Li yielded a tetranuclear oxo-bridged cluster, [U(μ-O)Cl(HO)], Na and K yielded two structurally distinct [U(HO)Cl] complexes, and Rb and Cs resulted in [UCl] as the dominant phases.
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