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New luminometric method for quantification of biological sulfur nucleophiles with the participation of 9‐cyano‐10‐methylacridinium salt

https://doi.org/10.1002/bio.4162
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Analysis of acetylcholine and choline in microdialysis samples by liquid chromatography/tandem mass spectrometry
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Density Functional Methods in Chemistry
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FIA titrations of sulphide, cysteine and thiol-containing drugs with chemiluminescent detection
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The influence of polarization functions on molecular orbital hydrogenation energies
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Penicillin: the medicine with the greatest impact on therapeutic outcomes
inferredcites →https://doi.org/10.1016/0022-2860(86)85315-7openalex-snapshot
Spectral evolution of the oxidation reaction-with alkaline hydrogen peroxide of lucigenin
inferredcites →https://doi.org/10.1016/j.aca.2003.11.032openalex-snapshot
Addition of nucleophiles to the 9-cyano-10-methylacridinium cation: utilization in their chemiluminescent assay
inferredcites →https://doi.org/10.1016/j.cplett.2004.06.011openalex-snapshot
A new hybrid exchange–correlation functional using the Coulomb-attenuating method (CAM-B3LYP)
inferredcites →https://doi.org/10.1016/j.talanta.2007.08.040openalex-snapshot
Enhancement of the chemiluminescence of penicillamine and ephedrine after derivatization with aldehydes using tris(bipyridyl)ruthenium(II) peroxydisulfate system and its analytical application
inferredcites →https://doi.org/10.1016/s0039-9140(99)00294-5openalex-snapshot
Chemiluminescence as diagnostic tool. A review
inferredcites →https://doi.org/10.1016/s0378-4347(97)00670-1openalex-snapshot
Analysis of cysteine and N-acetylcysteine in human plasma by high-performance liquid chromatography at the basal state and after oral administration of N-acetylcysteine
inferredcites →https://doi.org/10.1021/ac00276a046openalex-snapshot
Micelle-enhanced chemiluminescence and application to the determination of biological reductants using lucigenin
inferredcites →https://doi.org/10.1021/cr00031a013openalex-snapshot
Molecular Interactions in Solution: An Overview of Methods Based on Continuous Distributions of the Solvent
inferredcites →https://doi.org/10.1021/ct0499783openalex-snapshot
Using Hessian Updating To Increase the Efficiency of a Hessian Based Predictor-Corrector Reaction Path Following Method
inferredcites →https://doi.org/10.1021/jo0354387openalex-snapshot
Origin of Chemiluminescence Accompanying the Reaction of the 9-Cyano-10-methylacridinium Cation with Hydrogen Peroxide
inferredcites →https://doi.org/10.1021/jo1020882openalex-snapshot
Chemiluminogenic Features of 10-Methyl-9-(phenoxycarbonyl)acridinium Trifluoromethanesulfonates Alkyl Substituted at the Benzene Ring in Aqueous Media
inferredcites →https://doi.org/10.1039/a708863iopenalex-snapshot
Antioxidant chemistry Reactivity and oxidation of DL-cysteine by some common oxidants
inferredcites →https://doi.org/10.1039/an9891400401openalex-snapshot
Use of palladium(II) chloride as a colour-forming reagent for the determination of N-acetyl-L-cysteine in water and Fluimukan injections
inferredcites →https://doi.org/10.1039/an9962101569openalex-snapshot
Chemiluminescence determination of penicillamine via flow injection applying a Quinine–cerium( IV ) system
inferredcites →https://doi.org/10.1039/c4ra04095copenalex-snapshot
Nickel ferrite nanoparticles–hydrogen peroxide: a green catalyst-oxidant combination in chemoselective oxidation of thiols to disulfides and sulfides to sulfoxides
inferredcites →https://doi.org/10.1039/c5ob01798jopenalex-snapshot
Effective chemiluminogenic systems based on acridinium esters bearing substituents of various electronic and steric properties
inferredcites →https://doi.org/10.1063/1.2173258openalex-snapshot
Geometries and properties of excited states in the gas phase and in solution: Theory and application of a time-dependent density functional theory polarizable continuum model
inferredcites →https://doi.org/10.1063/1.474671openalex-snapshot
A new definition of cavities for the computation of solvation free energies by the polarizable continuum model
inferredcites →https://doi.org/10.1093/clinchem/29.8.1474openalex-snapshot
Acridinium esters as high-specific-activity labels in immunoassay.
inferredcites →https://doi.org/10.1093/clinchem/29.8.1480openalex-snapshot
Two-site immunochemiluminometric assay for human alpha 1-fetoprotein.
inferredcites →https://doi.org/10.1111/j.1751-1097.1965.tb09300.xopenalex-snapshot
CHEMILUMINESCENCE INVOLVING PEROXIDE DECOMPOSITIONS
inferredcites →https://doi.org/10.1111/j.1751-1097.2007.00140.xopenalex-snapshot
Development of a Quantitative Bio/Chemiluminescence Spectrometer Determining Quantum Yields: Re‐examination of the Aqueous Luminol Chemiluminescence Standard
inferredcites →https://doi.org/10.1134/s1061934812040028openalex-snapshot
Chemiluminescence determination of hydrogen peroxide
inferredcites →https://doi.org/10.17721/moca.2018.110-114openalex-snapshot
Determination Of N-Acetylcysteine In Tablets By Means Of Chemiluminescence Inhibition Method
inferredcites →https://doi.org/10.2116/analsci.10.449openalex-snapshot
Determination of Isoprenaline with Lucigenin Chemiluminescence Using Flow Injection Analysis
inferredcites →https://doi.org/10.2116/analsci.14.731openalex-snapshot
Chemiluminescence Detection of Thiols by High-Performance Liquid Chromatography Using o-Phthalaldehyde and N-(4-Aminobutyl)-N-ethylisoluminol as Precolumn Derivatization Reagents
inferredcites →https://doi.org/10.2298/jsc100904086sopenalex-snapshot
H5PV2Mo10O40 as an efficient catalyst for the oxidation of thiols to the corresponding disulfides using hydrogen peroxide as the oxidant
inferredcites →https://doi.org/10.3390/10101385openalex-snapshot
Urea- Hydrogen Peroxide (UHP) Oxidation of Thiols to the Corresponding Disulfides Promoted by Maleic Anhydride as Mediator

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4751208openalex-extracted
Aromatic Acridinium Thioesters as New Chemiluminescence Indicators In The Analysis of Biological Antioxidants
inferred← citeshttps://doi.org/10.1002/bio.4385openalex-snapshot
Preparation of a novel group of chemiluminescent N‐substituted acridinium esters
inferred← citeshttps://doi.org/10.1002/bio.4474openalex-snapshot
Synthesis, structure elucidation, and chemiluminescent activity of new 9‐substituted 10‐(ω‐(succinimidyloxycarbonyl)alkyl)acridinium esters
inferred← citeshttps://doi.org/10.1002/bio.4572openalex-snapshot
Synthesis and chemiluminescent characteristics of two new acridinium esters
inferred← citeshttps://doi.org/10.1016/j.jlumin.2024.120745openalex-snapshot
Aromatic acridinium thioesters–a new class of chemiluminogenic compounds and their interactions with some biological antioxidants
inferred← citeshttps://doi.org/10.3390/bios13040452openalex-snapshot
The Molecular Basis of Organic Chemiluminescence
inferred← citeshttps://doi.org/10.3390/chemosensors10050174openalex-snapshot
Development of a Coelenterazine Derivative with Enhanced Superoxide Anion-Triggered Chemiluminescence in Aqueous Solution
inferred← citeshttps://doi.org/10.3390/ijms23158490openalex-snapshot
Comparative Investigation of the Chemiluminescent Properties of a Dibrominated Coelenterazine Analog
inferred← citeshttps://doi.org/10.3390/molecules27248875openalex-snapshot
Combined Experimental and Theoretical Investigation into the Photophysical Properties of Halogenated Coelenteramide Analogs
inferred← citeshttps://doi.org/10.5650/jos.ess22327openalex-snapshot
Syntheses of Hindered-Polymethylacridinium Esters with Potential for Biological Probe Nanoarchitectonics
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