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Recent trends in chemistry, structure, and various applications of 1-acyl-3-substituted thioureas: a detailed review
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Unveiling the cyclopropyl appended acyl thiourea derivatives as antimicrobial, α-amylase and proteinase K inhibitors: Design, synthesis, biological evaluation, molecular docking, DFT and ADMET studies
inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.108319openalex-snapshot
Thiourea compounds as multifaceted bioactive agents in medicinal chemistry
inferred← citeshttps://doi.org/10.1016/j.bioorg.2025.109199openalex-snapshot
Computational and experimental investigations of novel 1,3-disubstituted thioureas as the dual inhibitor of b-TNAP and b-CAII enzyme for Cancer treatment
inferred← citeshttps://doi.org/10.1016/j.bpc.2023.107042openalex-snapshot
The influence of N-alkyl chains in benzoyl-thiourea derivatives on urease inhibition: Soil studies and biophysical and theoretical investigations on the mechanism of interaction
inferred← citeshttps://doi.org/10.1016/j.ccr.2023.215620openalex-snapshot
Platinum group metal (PGM) complexes having acylthiourea ligand system as catalysts or anticancer agents
inferred← citeshttps://doi.org/10.1016/j.cdc.2023.101025openalex-snapshot
Synthesis, in vitro acetylcholinesterase, butyrylcholinesterase activities and in silico molecular docking study of thiazole-thiourea hybrid derivatives
inferred← citeshttps://doi.org/10.1016/j.cdc.2026.101261openalex-snapshot
Conventional preparation method associated with ultrasonication process: spectral and crystallographic characterization of some acylthiourea compounds
inferred← citeshttps://doi.org/10.1016/j.fuel.2026.140494openalex-snapshot
Combustion performance and emission effects of a novel palladium thiourea additive in a diesel engine with EGR
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2024.134870openalex-snapshot
Multifaceted exploration of acylthiourea compounds: In vitro cytotoxicity, DFT calculations, molecular docking and dynamics simulation studies
inferred← citeshttps://doi.org/10.1016/j.inoche.2025.115143openalex-snapshot
Insights into structural and spectral properties of cobalt (II) complexes bearing asymmetric thiourea ligands and their remarkable bioactivities against Gram negative bacteria
inferred← citeshttps://doi.org/10.1016/j.inoche.2025.115798openalex-snapshot
Synthesis, crystal structures, and anti-pathogenic activity of cobalt(II) and zinc(II) N-Phenylpiperidine-1-carbothioamide complexes against fusarium oxysporum
inferred← citeshttps://doi.org/10.1016/j.inoche.2026.116837openalex-snapshot
Ru(II)-arene complexes of N-acyl thiourea-appended benzothiazoles: synthesis, characterization, anti-proliferative activity, molecular docking and ADMET profiling studies
inferred← citeshttps://doi.org/10.1016/j.jcat.2024.115633openalex-snapshot
CO2 hydrogenation to formic acid promoted by acylthiourea-ruthenium complexes with ionic liquid
inferred← citeshttps://doi.org/10.1016/j.jece.2024.114279openalex-snapshot
Acyl thiourea derivatives: Versatile tools for chemosensing and heavy metal remediation
inferred← citeshttps://doi.org/10.1016/j.jics.2026.103042openalex-snapshot
Common synthetic route associated with the ultrasonication process for amino acid incorporated acylthioureas preparation and their structural conformation by experimental and theoretical studies
inferred← citeshttps://doi.org/10.1016/j.jinorgbio.2025.113180openalex-snapshot
Synthesis, characterization, and anticancer activity of acylthiourea-ruthenium(II) p-cymene complexes
inferred← citeshttps://doi.org/10.1016/j.jinorgbio.2026.113405openalex-snapshot
Frontiers in Acylthiourea chemistry: Synthesis, metal complexation, and application potential
inferred← citeshttps://doi.org/10.1016/j.matchemphys.2026.133254openalex-snapshot
Investigating Gold Electrodes as a Sensory Warning System for Cochlear Implant Degradation
inferred← citeshttps://doi.org/10.1016/j.micpath.2024.107209openalex-snapshot
Computational and experimental insights into pharmacological potential: Synthesis, in vitro evaluation, and molecular docking analysis of bioactive urea and thiourea derivatives
inferred← citeshttps://doi.org/10.1016/j.molliq.2026.129751openalex-snapshot
A benzoyl-thiazole thiourea derivative photophysically observed: Unveiling the role of hydrogen bonding and solvent interactions
inferred← citeshttps://doi.org/10.1016/j.molstruc.2022.133721openalex-snapshot
Synthesis, X-Ray crystallography and HF/DFT analysis of N(diethylcarbamothioyl) furan-2-carboxamide, analyzed by experimental and theoretical methods
inferred← citeshttps://doi.org/10.1016/j.molstruc.2022.133839openalex-snapshot
Spectral, crystallographic, theoretical, and catalytic activity studies of the PdII complexes in different coordination modes of benzoylthiourea ligand
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.135797openalex-snapshot
Palladium(II) complexes derived from N,N'−diarylthiourea: Structural aspects and applications toward Suzuki-Miyaura coupling reactions
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.137585openalex-snapshot
In vitro and in silico correlation of bis-thiazole based Schiff base hybrids analogues: A computational approach develop to promising acetylcholinesterase and butyrylcholinesterase inhibitors
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.138726openalex-snapshot
Integrated insights into the synthesis and biological significances of novel benzofuran based oxadiazole/thiadiazole derivatives: A comprehensive computational and experimental study
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.139775openalex-snapshot
A novel class of thiazole based thiadiazole hybrids: The privileged scaffolds of potent anti-Alzheimer's activity along with molecular docking and ADME analysis
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.141120openalex-snapshot
Synthesis, characterization, antioxidant, antibacterial activity, and molecular docking studies of Zn (II) and Cu (II) complexes nanoparticles
inferred← citeshttps://doi.org/10.1016/j.molstruc.2025.145070openalex-snapshot
Fluoro-substituted benzoylthiourea derivatives: Synthesis, structural characterization, and evaluation of antioxidant and antimicrobial activities
inferred← citeshttps://doi.org/10.1016/j.poly.2022.116055openalex-snapshot
Synthesis, structural characterization and catalytic application of zinc and cadmium sulfur complexes with imidazol-2-ylidene-N’-phenylthiourea ligand scaffold
inferred← citeshttps://doi.org/10.1016/j.poly.2022.116076openalex-snapshot
Platinum(II) complexes bearing asymmetrically substituted pivaloylthioureas: Synthesis, crystal structures, DFT and antioxidant studies
inferred← citeshttps://doi.org/10.1016/j.poly.2023.116707openalex-snapshot
Ruthenium(III) acyl thiourea complex: A catalyst for transfer hydrogenation of nitroarenes
inferred← citeshttps://doi.org/10.1016/j.rechem.2026.103841openalex-snapshot
Coordination versatility in palladium(II) complexes bearing substituted naphthoylthioureas: crystal structures, Hirshfeld surface analysis, DFT and molecular docking studies
inferred← citeshttps://doi.org/10.1016/j.sna.2022.113967openalex-snapshot
Highly efficient and fast electrochemical sensor based on aluminium oxide (Al2O3) nanoparticle for the detection of organosulfur compounds
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c04448openalex-snapshot
Pinonic Acid Derivatives Containing Thiourea Motif: Promising Antifungal Lead Compound Targeting Cellular Barrier of Colletotrichum fructicola
inferred← citeshttps://doi.org/10.1021/acs.jafc.5c00430openalex-snapshot
Thiourea Derivatives in Agrochemical Discovery and Development
inferred← citeshttps://doi.org/10.1021/acsami.6c06620openalex-snapshot
An Abiotic Cu/COOH Nanozyme for Cellulose Depolymerization and One-Pot Conversion into a Triazole Surfactant in Neutral Water
inferred← citeshttps://doi.org/10.1021/acsomega.5c11616openalex-snapshot
Novel Phenethylamine-Based Aroyl Thiourea Derivatives: Design, Synthesis, and Multibiological Evaluation
inferred← citeshttps://doi.org/10.1021/acsomega.6c07002openalex-snapshot
Integrated Experimental and Computational Investigation of Fluorinated Benzoylthiourea Derivatives: Structural Characterization, Hirshfeld Surface Analysis, Antioxidant Activity, and MAO–B Inhibitory Potential for Parkinson’s Disease
inferred← citeshttps://doi.org/10.1039/d2ra03160dopenalex-snapshot
Structure and surface analyses of a newly synthesized acyl thiourea derivative along with its in silico and in vitro investigations for RNR, DNA binding, urease inhibition and radical scavenging activities
inferred← citeshttps://doi.org/10.1039/d3cc06118copenalex-snapshot
Recent advancement in the synthesis of isothiocyanates
inferred← citeshttps://doi.org/10.1039/d3md00508aopenalex-snapshot
Synthesis, biological and molecular modelling for 1,3,4-thiadiazole sulfonyl thioureas: bacterial and fungal activity
inferred← citeshttps://doi.org/10.1039/d3nj04443bopenalex-snapshot
Synthesis, antimicrobial activity and molecular simulation of thiourea derivatives containing 6-carboalkoxybenzo[ d ]thiazole and d -glucose moieties
inferred← citeshttps://doi.org/10.1039/d3ob01584jopenalex-snapshot
Isothiocyanates ( in situ ) and sulfonyl chlorides in water for N -functionalization of bicyclic amidines: access to N -alkylated γ-/ω-lactam derivatized thiourea and sulfonamides
inferred← citeshttps://doi.org/10.1039/d3qm00540bopenalex-snapshot
Carbohydrate–macrocycle conjugates for biomedical applications
inferred← citeshttps://doi.org/10.1039/d4cc01666aopenalex-snapshot
Synthesis of N -β-brominated alkenyl isothiocyanates via dehydrogenation of alkyl isothiocyanates
inferred← citeshttps://doi.org/10.1039/d4md00334aopenalex-snapshot
Design, synthesis, inhibitory activity, and molecular simulations study for d -glucose-conjugated thioureas containing pyrimidine ring as multitarget inhibitors against α-amylase, α-glucosidase, DDP-4, and PTP1B in Type 2 diabetes mellitus
inferred← citeshttps://doi.org/10.1039/d4nj00209aopenalex-snapshot
Synthesis, anticancer activity, and molecular simulation of N -(2,3,4,6-tetra- O -acetyl-β- d -glucopyranosyl)thioureas containing a pyrimidine ring
inferred← citeshttps://doi.org/10.1039/d4nj01174kopenalex-snapshot
The short route to chalcogenurea-substituted 3 a ,6-epoxyisoindoles via an intramolecular Diels–Alder furan (IMDAF) reaction. Antibacterial and antifungal activity
inferred← citeshttps://doi.org/10.1039/d4ra02567aopenalex-snapshot
Exploring the latest trends in chemistry, structure, coordination, and diverse applications of 1-acyl-3-substituted thioureas: a comprehensive review
inferred← citeshttps://doi.org/10.1039/d6md00026fopenalex-snapshot
d -Galactose-conjugated pyrimidine thioureas as potent antimicrobial agents: rapid green synthesis, structure–activity relationships and molecular modelling
inferred← citeshttps://doi.org/10.1039/d6na00422aopenalex-snapshot
Zinc nanozymes for hydrolytic degradation of di(2-ethylhexyl) phthalate (DEHP)
inferred← citeshttps://doi.org/10.1063/5.0332726openalex-snapshot
Synthesis, anti-breast cancer, DFT and molecular docking study of some new thiourea benzamide derivatives
inferred← citeshttps://doi.org/10.1080/00958972.2023.2292476openalex-snapshot
Copper(II) complexes with N,O-coordinating thiopseudoureas: syntheses, structures, and properties
inferred← citeshttps://doi.org/10.1080/00958972.2025.2583368openalex-snapshot
A newly developed cobalt(II) complex derived from a thiourea derivative and assessment of its potential bioapplicability against plant root pathogens
inferred← citeshttps://doi.org/10.1080/03067319.2024.2371999openalex-snapshot
Efficient and sustainable design of pyridyl-bis-thiourea pincer ligand-immobilised Merrifield polymer precursor for arsenic ions adsorption
inferred← citeshttps://doi.org/10.1080/03067319.2025.2505934openalex-snapshot
Sustainable recovery of silver from X-ray film processing effluents using a novel thiourea derivative-grafted XAD-7 resin and its application in nano silver particle synthesis
inferred← citeshttps://doi.org/10.1080/10426507.2022.2152814openalex-snapshot
3,3-Disubstituted 1-acylthioureas as ionophores for Pb(II)-ion selective electrodes: physical and chemical characterization of the sensing membranes
inferred← citeshttps://doi.org/10.1080/10426507.2023.2201503openalex-snapshot
Novel thiourea derivatives against Mycobacterium tuberculosis: synthesis, characterization and molecular docking studies
inferred← citeshttps://doi.org/10.1080/10426507.2025.2457458openalex-snapshot
Review on the synthesis of thiourea-triazine hybrid derivatives and its applications primarily in biological context
inferred← citeshttps://doi.org/10.1080/10426507.2025.2574290openalex-snapshot
Synthesis, X-ray crystal structures, spectroscopic characterization, DFT calculations, and molecular docking study of new N -(4-chlorobutanoyl)- N’ -(2-, 3-, and 4-methoxyphenyl)thiourea derivatives
inferred← citeshttps://doi.org/10.1080/16583655.2023.2245200openalex-snapshot
Synthesis of phenylthiourea-based pyrazole, thiazole and/or pyran compounds: molecular modeling and biological activity
inferred← citeshttps://doi.org/10.1080/17415993.2026.2651242openalex-snapshot
Comprehensive review on the synthesis of isothiocyanates via desulfurization
inferred← citeshttps://doi.org/10.1080/17415993.2026.2700323openalex-snapshot
Syntheses and biological applications of thiourea derivatives: developments and challenges
inferred← citeshttps://doi.org/10.1080/17568919.2025.2504332openalex-snapshot
Synthesis, antimicrobial evaluation, HPLC-based compound accumulation and docking studies of 2-methoxybenzoyl thioureas
inferred← citeshttps://doi.org/10.1107/s2053229625000282openalex-snapshot
Synthesis and diverse crystal packing in o -, m - and p -bis(carbonylthioureido)benzenes containing bisferrocenes
inferred← citeshttps://doi.org/10.1107/s2056989022012245openalex-snapshot
Synthesis, characterization, and crystal structures of N , N ′-bis(2-dialkylaminophenyl)thioureas
inferred← citeshttps://doi.org/10.1107/s2056989024005449openalex-snapshot
Crystal structure of tris{ N , N -diethyl- N ′-[(4-nitrophenyl)(oxo)methyl]carbamimidothioato}cobalt(III)
inferred← citeshttps://doi.org/10.1134/s1070363224110264openalex-snapshot
Acid Ionization Constants of Some N-Benzoylthiourea-Pyrrolidine Derivatives Bearing an Indole Ring by Potentiometric Titration in DMSO–Water
inferred← citeshttps://doi.org/10.1515/pac-2025-0699openalex-snapshot
Benzoyl thiourea-derived chemosensor for colorimetric and fluorescent detection of Cu 2+ in water and soils
inferred← citeshttps://doi.org/10.1515/zpch-2025-0147openalex-snapshot
Acylthiourea derivatives for the colorimetric detection of Cu(II), Hg(II) and Fe(III) in aqueous solution
inferred← citeshttps://doi.org/10.15446/rev.colomb.quim.v52n1.108362openalex-snapshot
Síntesis de tioureas con isoniacida y niacida estructural: test frente a bacterias Gram + y Gram –
inferred← citeshttps://doi.org/10.1584/jpestics.d23-034openalex-snapshot
The structure–activity relationship of aryloxyacetylthioureas for the inhibition of Orobanche minor radicle elongation
inferred← citeshttps://doi.org/10.18596/jotcsa.1269213openalex-snapshot
Synthesis and Determination of Acid Dissociation Constants of Bis-Acyl Thiourea Derivatives
inferred← citeshttps://doi.org/10.21123/bsj.2023.7745openalex-snapshot
Preparation, characterization, antioxidant activity of 1-(2-furoyl) thiourea derivatives and study the molecular docking of them as potent inhibitors of Urease enzyme
inferred← citeshttps://doi.org/10.2139/ssrn.6507309openalex-snapshot
Electrochemical Isothiocyanation of Biomass-Based Amines over Co Catalyst
inferred← citeshttps://doi.org/10.2139/ssrn.7571361openalex-snapshot
Electrochemical Isothiocyanation of Biomass-Based Amines over Co Catalyst
inferred← citeshttps://doi.org/10.2174/0118715206330232240913100744openalex-snapshot
Acyl Urea Compounds Therapeutics and its Inhibition for Cancers in Women: A Review
inferred← citeshttps://doi.org/10.29048/makufebed.1397481openalex-snapshot
Buji İle Ateşlemeli Bir Motorda Benzoiltiyoüre Türevi Yakıt Katkısının Motor Performansı ve Egzoz Emisyonlarına Etkisinin İncelenmesi
inferred← citeshttps://doi.org/10.3389/fchem.2022.992701openalex-snapshot
Facile synthesis, crystal structure, biological evaluation, and molecular modeling studies of N-((4-acetyl phenyl) carbamothioyl) pivalamide as the multitarget-directed ligand
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1040671openalex-snapshot
Synergistic antifungal interaction of N-(butylcarbamothioyl) benzamide and amphotericin B against Cryptococcus neoformans
inferred← citeshttps://doi.org/10.3390/ijms232415694openalex-snapshot
Synthesis, Structural Characterization and Biological Activity Evaluation of Novel Cu(II) Complexes with 3-(trifluoromethyl)phenylthiourea Derivatives
inferred← citeshttps://doi.org/10.3390/molecules28062707openalex-snapshot
Investigation of Newly Synthesized Bis-Acyl-Thiourea Derivatives of 4-Nitrobenzene-1,2-Diamine for Their DNA Binding, Urease Inhibition, and Anti-Brain-Tumor Activities
inferred← citeshttps://doi.org/10.3390/molecules29204906openalex-snapshot
Novel Thiourea Ligands—Synthesis, Characterization and Preliminary Study on Their Coordination Abilities
inferred← citeshttps://doi.org/10.3390/pharmaceutics15102501openalex-snapshot
Contribution to the Synthesis, Characterization, Separation and Quantification of New N-Acyl Thiourea Derivatives with Antimicrobial and Antioxidant Potential
inferred← citeshttps://doi.org/10.4155/fmc-2023-0168openalex-snapshot
Evaluation of Synthetic Aminoquinoline Derivatives As Urease Inhibitors: In Vitro , In Silico and Kinetic Studies
inferred← citeshttps://doi.org/10.5155/eurjchem.17.3.268-279.2815openalex-snapshot
Crystal structure and supramolecular assembly of a hydrogen-bonded cocrystal of 2-fluoro-N-(pyrrolidine-1-carbonothioyl)benzamide and 1,3,5-triazinane-2,4,6-trithione
inferred← citeshttps://doi.org/10.70675/8a9b378cz83a3z42f8za20bzdd25e08822b5openalex-snapshot
Conception de médicaments contre le virus de la bronchiolite à partir d'une nouvelle cible thérapeutique
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