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Aromatic Acridinium Thioesters as New Chemiluminescence Indicators In The Analysis of Biological Antioxidants

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inferredcites →https://doi.org/10.1002/agt2.140openalex-extracted
Chemiluminescence: From mechanism to applications in biological imaging and therapy
inferredcites →https://doi.org/10.1002/bio.2555openalex-extracted
Development of a highly sensitive chemiluminescent assay for hydrogen peroxide under neutral conditions using acridinium ester and its application to an enzyme immunoassay
inferredcites →https://doi.org/10.1002/bio.3629openalex-extracted
On the use of acridinium indicators for the chemiluminescent determination of the total antioxidant capacity of dietary supplements
inferredcites →https://doi.org/10.1002/bio.4162openalex-extracted
New luminometric method for quantification of biological sulfur nucleophiles with the participation of 9‐cyano‐10‐methylacridinium salt
inferredcites →https://doi.org/10.1002/cphc.202200166openalex-extracted
Solvent Effect on the Chemiluminescence of Acridinium Thioester: A Computational Study
inferredcites →https://doi.org/10.1002/elan.201600209openalex-extracted
Electrochemiluminescence of Acridines
inferredcites →https://doi.org/10.1002/j.1939-4640.2003.tb02726.xopenalex-extracted
Enhanced Chemiluminescence Assay vs Colorimetric Assay for Measurement of the Total Antioxidant Capacity of Human Seminal Plasma
inferredcites →https://doi.org/10.1002/qua.25881openalex-extracted
Mechanistic insights into the efficient intramolecular chemiexcitation of dioxetanones from TD‐DFT and multireference calculations
inferredcites →https://doi.org/10.1007/978-1-4612-3136-3openalex-extracted
Density Functional Methods in Chemistry
inferredcites →https://doi.org/10.1007/bf00533485openalex-extracted
The influence of polarization functions on molecular orbital hydrogenation energies
inferredcites →https://doi.org/10.1007/s00204-015-1579-5openalex-extracted
Redox- and non-redox-metal-induced formation of free radicals and their role in human disease
inferredcites →https://doi.org/10.1007/s00216-011-5455-8openalex-extracted
Analytical chemiluminescence and bioluminescence: latest achievements and new horizons
inferredcites →https://doi.org/10.1016/0003-2697(91)90542-2openalex-extracted
Acridine orange as a probe for measuring pH gradients across membranes: Mechanism and limitations
inferredcites →https://doi.org/10.1016/j.aca.2003.11.032openalex-extracted
Addition of nucleophiles to the 9-cyano-10-methylacridinium cation: utilization in their chemiluminescent assay
inferredcites →https://doi.org/10.1016/j.aca.2009.03.017openalex-extracted
Chemiluminescence detection in liquid chromatography: Applications to clinical, pharmaceutical, environmental and food analysis—A review
inferredcites →https://doi.org/10.1016/j.diagmicrobio.2016.05.013openalex-extracted
A novel chemiluminescent immunoassay for detection of Toxoplasma gondii IgG in human sera
inferredcites →https://doi.org/10.1016/j.ejmech.2012.04.040openalex-extracted
Synthesis and biological activity of novel mycophenolic acid conjugates containing nitro-acridine/acridone derivatives
inferredcites →https://doi.org/10.1016/j.jlumin.2017.02.068openalex-extracted
Chemiluminogenic acridinium salts: A comparison study. Detection of intermediate entities appearing upon light generation
inferredcites →https://doi.org/10.1016/j.jlumin.2017.10.025openalex-extracted
Combined experimental and theoretical study of Coelenterazine chemiluminescence in aqueous solution
inferredcites →https://doi.org/10.1016/j.saa.2010.10.029openalex-extracted
1H and 13C NMR spectra, structure and physicochemical features of phenyl acridine-9-carboxylates and 10-methyl-9-(phenoxycarbonyl)acridinium trifluoromethanesulphonates – alkyl substituted in the phenyl fragment
inferredcites →https://doi.org/10.1016/j.tibtech.2004.03.011openalex-extracted
Biotechnological applications of bioluminescence and chemiluminescence
inferredcites →https://doi.org/10.1016/j.trac.2008.12.006openalex-extracted
Chemiluminescence immunoassay
inferredcites →https://doi.org/10.1016/j.trac.2010.07.001openalex-extracted
Nanoparticle-assisted chemiluminescence and its applications in analytical chemistry
inferredcites →https://doi.org/10.1016/j.trac.2013.01.013openalex-extracted
Nanosized labels for rapid immunotests
inferredcites →https://doi.org/10.1016/j.trac.2015.07.004openalex-extracted
Advances in the application of chemiluminescence detection in liquid chromatography
inferredcites →https://doi.org/10.1016/j.vascn.2017.09.256openalex-extracted
A novel luminol-based enhanced chemiluminescence antioxidant capacity microplate assay for use in different biological matrices
inferredcites →https://doi.org/10.1016/s0003-2670(03)00809-2openalex-extracted
Clinical applications of chemiluminescence
inferredcites →https://doi.org/10.1016/s0003-2670(98)00747-8openalex-extracted
On-line screening method for antioxidants by liquid chromatography with chemiluminescence detection
inferredcites →https://doi.org/10.1021/acs.bioconjchem.9b00391openalex-extracted
Recent Advances of Molecular Optical Probes in Imaging of β-Galactosidase
inferredcites →https://doi.org/10.1021/acs.jafc.7b05830openalex-extracted
Antioxidants: Differing Meanings in Food Science and Health Science
inferredcites →https://doi.org/10.1021/ar00072a001openalex-extracted
The path of chemical reactions - the IRC approach
inferredcites →https://doi.org/10.1021/cr00031a013openalex-extracted
Molecular Interactions in Solution: An Overview of Methods Based on Continuous Distributions of the Solvent
inferredcites →https://doi.org/10.1021/cr9001098openalex-extracted
Solvent-Free Heterocyclic Synthesis
inferredcites →https://doi.org/10.1021/ed074p1208openalex-extracted
Molecular Photophysics of Acridine Yellow Studied by Phosphorescence and Delayed Fluorescence: An Undergraduate Physical Chemistry Experiment
inferredcites →https://doi.org/10.1021/j100527a014openalex-extracted
Intersystem crossing and internal conversion quantum yields of acridine in polar and nonpolar solvents
inferredcites →https://doi.org/10.1021/jo1020882openalex-extracted
Chemiluminogenic Features of 10-Methyl-9-(phenoxycarbonyl)acridinium Trifluoromethanesulfonates Alkyl Substituted at the Benzene Ring in Aqueous Media
inferredcites →https://doi.org/10.1021/jo980566uopenalex-extracted
Toward an Understanding of the Chemiluminescence Accompanying the Reaction of 9-Carboxy-10-methylacridinium Phenyl Ester with Hydrogen Peroxide
inferredcites →https://doi.org/10.1021/jp104253fopenalex-extracted
Chemiluminogenic Properties of 10-Methyl-9-(phenoxycarbonyl)acridinium Cations in Organic Environments
inferredcites →https://doi.org/10.1039/9781849732024-00051openalex-extracted
The Nature of Chemiluminescent Reactions
inferredcites →https://doi.org/10.1039/b810189bopenalex-extracted
Long-range corrected hybrid density functionals with damped atom–atom dispersion corrections
inferredcites →https://doi.org/10.1039/c19680001533openalex-extracted
Alkylations with methyl and ethyl fluorosulphonates
inferredcites →https://doi.org/10.1039/c5ob01798jopenalex-extracted
Effective chemiluminogenic systems based on acridinium esters bearing substituents of various electronic and steric properties
inferredcites →https://doi.org/10.1039/c7ra01026eopenalex-extracted
Recent developments in the synthesis and biological activity of acridine/acridone analogues
inferredcites →https://doi.org/10.1039/d0cs00348dopenalex-extracted
Chemiluminescence for bioimaging and therapeutics: recent advances and challenges
inferredcites →https://doi.org/10.1039/d1nj03440eopenalex-extracted
Elucidating the chemiexcitation of dioxetanones by replacing the peroxide bond with S–S, N–N and C–C bonds
inferredcites →https://doi.org/10.1063/1.2173258openalex-extracted
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-extracted
A new definition of cavities for the computation of solvation free energies by the polarizable continuum model
inferredcites →https://doi.org/10.1093/clinchem/31.10.1664openalex-extracted
Chemiluminescence immunoassay of plasma progesterone, with progesterone-acridinium ester used as the labeled antigen.
inferredcites →https://doi.org/10.1093/clinchem/41.9.1368openalex-extracted
Lumigen→ PS: Chemiluminescent Detection of Horseradish Peroxidase by Enzymatic Generation of Acridinium Esters
inferredcites →https://doi.org/10.1111/jfbc.14264openalex-extracted
Health benefits of polyphenols: A concise review
inferredcites →https://doi.org/10.1146/annurev.nu.16.070196.000341openalex-extracted
Antioxidants in Human Health and Disease
inferredcites →https://doi.org/10.15406/jabb.2019.06.00173openalex-extracted
Oxidative stress and antioxidant mechanisms in human body
inferredcites →https://doi.org/10.2174/0929867023369277openalex-extracted
Acridine Derivatives as Chemotherapeutic Agents
inferredcites →https://doi.org/10.2174/1566524022666211222161637openalex-extracted
Free Radicals and Oxidative Stress: Signaling Mechanisms, Redox Basis for Human Diseases, and Cell Cycle Regulation
inferredcites →https://doi.org/10.3389/fonc.2019.00925openalex-extracted
Acridine Orange: A Review of Novel Applications for Surgical Cancer Imaging and Therapy
inferredcites →https://doi.org/10.3390/chemosensors12020025openalex-extracted
Easy-to-Use Chemiluminescent-Based Assay for a Rapid and Low-Cost Evaluation of the Antioxidant Activity of Cosmetic Products
inferredcites →https://doi.org/10.3390/ijms21124417openalex-extracted
Computational Insights on the Mechanism of the Chemiluminescence Reaction of New Group of Chemiluminogens—10-Methyl-9-thiophenoxycarbonylacridinium Cations
inferredcites →https://doi.org/10.3390/ijms22073380openalex-extracted
Analytical Methods Used in Determining Antioxidant Activity: A Review
inferredcites →https://doi.org/10.3390/ijms23137273openalex-extracted
Oxidative Stress in Ageing and Chronic Degenerative Pathologies: Molecular Mechanisms Involved in Counteracting Oxidative Stress and Chronic Inflammation
inferredcites →https://doi.org/10.5650/jos.ess21186openalex-extracted
Acridinium Ester Chemiluminescence: Methyl Substitution on the Acridine Moiety
inferredcites →https://doi.org/10.5702/massspec.44.175openalex-extracted
Mass Spectrometric Investigation of Structures of Intermediates in Acridine Chemiluminescence.
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