4.5 Article

Synthesis, structure elucidation, and chemiluminescent activity of new 9-substituted 10-(ω-(succinimidyloxycarbonyl)alkyl)acridinium esters

Related references

Note: Only part of the references are listed.
Article Chemistry, Analytical

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

Vladyslav Ievtukhov et al.

Summary: A luminometric method was developed to quantify biologically active compounds containing sulfhydryl groups by oxidizing a specific substrate in the presence of RSHs and oxygen, generating chemiluminescence with no need for hydrogen peroxide. The detection limits were low and the produced light was linearly proportional to the analyte content, suggesting potential applications in quantifying these compounds in various systems.

LUMINESCENCE (2022)

Article Chemistry, Applied

Acridinium Ester Chemiluminescence: Methyl Substitution on the Acridine Moiety

Manabu Nakazono et al.

Summary: The introduction of methyl groups in acridinium esters can shift the optimal pH for relatively strong chemiluminescence from neutral to alkaline conditions. Certain compounds exhibit long-lasting chemiluminescence under alkaline conditions, which could be used for detecting hydrogen peroxide concentration.

JOURNAL OF OLEO SCIENCE (2021)

Review Immunology

Chemiluminescent immunoassay technology: what does it change in autoantibody detection?

Luigi Cinquanta et al.

AUTOIMMUNITY HIGHLIGHTS (2017)

Article Chemistry, Organic

A comparison of chemiluminescent acridinium dimethylphenyl ester labels with different conjugation sites

Anand Natrajan et al.

ORGANIC & BIOMOLECULAR CHEMISTRY (2015)

Article Chemistry, Multidisciplinary

Synthesis and properties of chemiluminescent acridinium esters with different N-alkyl groups

Shenliang Wang et al.

RSC ADVANCES (2015)

Article Chemistry, Organic

Synthesis and properties of differently charged chemiluminescent acridinium ester labels

Anand Natrajan et al.

ORGANIC & BIOMOLECULAR CHEMISTRY (2013)

Article Chemistry, Multidisciplinary

Simultaneous Quantification of Multiple Nucleic Acid Targets Using Chemiluminescent Probes

Kenneth A. Browne et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2011)

Article Chemistry, Physical

Synthesis and properties of novel chemiluminescent biological probes: 2- and 3-(2-Succinimidyloxycarbonylethyl)phenyl acridinium esters

Keith Smith et al.

JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY (2009)

Article Biochemistry & Molecular Biology

Carp (Cyprinus carpio) vitellogenin:: purification and development of a simultaneous chemiluminescent immunoassay

H Fukada et al.

COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY A-MOLECULAR & INTEGRATIVE PHYSIOLOGY (2003)

Article Biochemical Research Methods

Single-nucleotide polymorphism analysis by hybridization protection assay on solid support

S Goto et al.

ANALYTICAL BIOCHEMISTRY (2002)

Review Chemistry, Analytical

Chemiluminescence as a diagnostic tool. A review

C Dodeigne et al.

TALANTA (2000)