Herein, we report a series of selective sub-nanomolar inhibitors against butyrylcholinesterase (BChE). These compounds, bearing a novel -benzyl benzamide scaffold, inhibited BChE with IC from picomolar to nanomolar. The inhibitory activity was confirmed by the surface plasmon resonance assay, showing a sub-nanomolar value, which revealed that the compounds exert the inhibitory effect through directly binding to BChE. Several compounds showed neuroprotective effects verified by the oxidative damage model. Furthermore, the safety of and was demonstrated by the in vivo acute toxicity test. In the behavior study, 0.5 mg/kg or exhibited a marked therapeutic effect, which was almost equal to the treatment with 1 mg/kg rivastigmine, against the cognitive impairment induced by Aβ. The pharmacokinetics studies characterized the metabolic stability of . Thus, -benzyl benzamide inhibitors are promising compounds with drug-like properties for improving cognitive dysfunction, providing a potential strategy for the treatment of Alzheimer's disease.
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http://dx.doi.org/10.1021/acs.jmedchem.2c00944 | DOI Listing |
Aliment Pharmacol Ther
January 2025
Gastroenterology and Hepatology Unit, Department of Medicine, Faculty of Medicine, Universiti Malaya, Kuala Lumpur, Malaysia.
Background: International guidelines recommend contrasting initial treatment strategies for functional dyspepsia (FD).
Aims: To evaluate the efficacy and safety of treatment according to subtypes, compared with empirical proton pump inhibitor (PPI), in the initial treatment of FD.
Methods: We performed a single-blinded, randomised controlled trial of adults with FD.
Chem Asian J
November 2024
Department of Chemistry, St. Xavier's College (Autonomous), Kolkata, 700016, India.
The bidentate N, N, donor phenyl-azo-naphthaldoxime NpLH, 1 was used to synthesize the ruthenium(II) complex trans-[Ru(NpL)(CO)Cl(PPh)], 2. It has been characterized by SCXRD, electrochemical and spectral studies. Computational analysis indicates that the low-lying π*-LUMO of the complex has substantial azo-character of coordinated ligand.
View Article and Find Full Text PDFInt J Pharm
January 2025
Departamento de Farmacología, Farmacia y Tecnología Farmacéutica, I+D Farma (GI-1645), Faculty of Pharmacy, iMATUS, and Health Research Institute of Santiago de Compostela (IDIS), Universidade de Santiago de Compostela, Santiago de Compostela 15782, Spain. Electronic address:
Heme oxygenase-1 (HO-1) has been identified as a potential new target in anticancer therapy, being overexpressed in different tumors and crucial for cell proliferation. Advances in the development of specific HO-1 inhibitors should support the understanding of controlling HO-1 activity as antitumoral strategies, opening the path for future therapeutic applications. In the present study, small series of new HO-1 inhibitors were synthesized by joining a butylimidazolic pharmacophore together with a hydrophobic moiety spaced by a 2-oxybenzamide central linker.
View Article and Find Full Text PDFDalton Trans
November 2024
Phosphorus Laboratory, Department of Chemistry, Indian Institute of Technology, Bombay, Powai, Mumbai 400076, India.
In this article, the synthesis of bis(phosphine), -PhPCHC(O)N(H)CHCHPPh- (1) (hereafter referred to as "PNHP" and its anionic form as "PNP") and its group 10 metal chemistry and catalytic studies are described. PNHP (1) on reaction with NiCl(DME) and PdCl(COD) afforded pincer complexes, [MCl{(PNP)κ-,,}] (M = Ni, 2; Pd, 3). A similar reaction of 1 with PtCl(COD) yielded a chelate complex, [PtCl{(PNHP)κ-,}] (4), which on further treatment with LiHMDS produced the 1,2-azaphospholene-phosphine complex, [PtCl(Ph){(-P(Ph)CHCONCHCHPPh-)κ-,}] (5) P-C/P-N bond metathesis.
View Article and Find Full Text PDFJ Occup Health
January 2024
Osaka Occupational Health Service Center, Japan Industrial Safety and Health Association, 2-3-8 Tosabori, Nishi-Ku, Osaka 550-0001, Japan.
Objective: We aimed to develop a reliable gas chromatography-mass spectrometry (GC-MS) method for detecting urinary benzyl alcohol (BeOH) concentrations and assess the suitability of urinary BeOH as a biomarker for occupational BeOH exposure.
Methods: Thirteen male participants exposed to BeOH during paint-stripping work provided preshift and postshift urine samples, and their personal exposure concentrations were measured. Meanwhile, a control group of 10 nonexposed workers contributed urine samples.
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