The 3-aminophthalic acid anion is a light emitter in luminol chemiluminescence. In the present study, the chemiluminescence of the 3-aminophthalic acid anion itself in the presence of hydrogen peroxide-cobalt (II) was studied. The results indicated that 3-aminophthalic acid anion is highly chemiluminescent in the typical hydrogen peroxide-cobalt (II) system. The peak wavelength of this chemiluminescence and the kinetic profile of the 3-aminophthalic acid anion-hydrogen peroxide-cobalt (II) reaction showed similarity with that of luminol, but the chemiluminescence of 3-aminophthalic acid anion had a much lower background signal. In addition, the chemiluminescence mechanism of 3-aminophthalic acid anion-hydrogen peroxide-cobalt (II) was also discussed and speculated as the interaction between 3-aminophthalic acid anion and singlet oxygen.
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http://dx.doi.org/10.1002/bio.3740 | DOI Listing |
Food Chem
June 2024
School of Food and Bioengineering, Xihua University, Chengdu 610039, China; Food Microbiology Key Laboratory of Sichuan Province, China; Chongqing Key Laboratory of Speciality Food Co-Built by Sichuan and Chongqing, China. Electronic address:
In this study, a dual-mode colorimetric/CL nanosensor was developed for glyphosate detection based on the specific inhibition of FeO@Cu peroxidase-like activity. Synthesized FeO@Cu exhibited high levels of peroxidase-like activity that triggered the oxidation of luminol/3,3',5,5'-tetramethyl benzidine dihydrochloride (TMB) to excited-state 3-aminophthalic acid/blue oxTMB, thereby delivering a CL signal/visible colorimetric signal, however, the presence of glyphosate inhibited this activity, resulting in a decrease in signal strength. In-depth investigation revealed that this inhibitory mechanism occurs via two pathways: one in which glyphosate chelates with Fe(III)/Cu(II) and occupy the catalytical active sites of FeO@Cu, thereby decreasing the generation of OH, and another in which glyphosate competes with TMB to consume generated OH, thus reducing the oxidation of TMB.
View Article and Find Full Text PDFChem Commun (Camb)
February 2022
Department of Biochemistry and Molecular Biology, Mayo Clinic College of Medicine and Science, Rochester, MN 55905, USA.
In this study, we identified 3-aminophthalic acid as a new ligand of cereblon (CRBN) E3 ubiquitin ligase and developed a phthalic acid-based O'PROTAC for degradation of the ERG transcription factor. This phthalic acid-based O'PROTAC presented an efficacy in degrading ERG comparable to those displayed by pomalidomide-based ERG O'PROTACs. Moreover, phthalic acid-being more chemically stable and economical than classical immunomodulatory drugs (IMiDs)-represents, as a ligand, a new alternative for the development of PROTACs, especially O'PROTACs.
View Article and Find Full Text PDFLuminescence
May 2020
College of Materials and Chemistry & Chemical Engineering, Mineral Resources Chemistry Key Laboratory of Sichuan Higher Education Institution, Chengdu University of Technology, Chengdu, Sichuan, China.
The 3-aminophthalic acid anion is a light emitter in luminol chemiluminescence. In the present study, the chemiluminescence of the 3-aminophthalic acid anion itself in the presence of hydrogen peroxide-cobalt (II) was studied. The results indicated that 3-aminophthalic acid anion is highly chemiluminescent in the typical hydrogen peroxide-cobalt (II) system.
View Article and Find Full Text PDFBioorg Med Chem Lett
October 2014
Pharmaceutical Research Center, Meiji Seika Pharma, Co., Ltd, 760 Morooka-cho, Kohoku-ku, Yokohama 222-8567, Japan.
3-(4-Hydroxypiperidine-1-yl) phthalic acid 1 shows potent inhibitory activity against metallo-β-lactamase, which is known to inactivate β-lactam antibiotics such as carbapenems. Here, the structure of co-crystals of the metallo-β-lactamase IMP-1 and 1 was first analyzed by X-ray crystallography, and then used for structure-based drug design. Four novel compounds bearing substituents at the 6-position were synthesized to produce 3,6-disubstituted phthalic acid derivatives, and their IMP-1 inhibitory activity and synergistic effect with the carbapenem biapenem (BIPM) were evaluated.
View Article and Find Full Text PDFXenobiotica
March 2000
Laboratory of Pharmacology and Chemistry, National Toxicology Program, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.
1. The metabolism and disposition of Luminol (LMN, 3-aminophthalhydrazide), a widely used forensic and laboratory reagent that chemiluminesses upon oxidation, was determined as part of its overall toxicological characterization. 2.
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