Coumarin compounds represent an important type of naturally occurring and synthetic oxygen-containing heterocycles with typical benzopyrone framework. This type of special benzopyrone structure enables its derivatives readily interact with a diversity of enzymes and receptors in organisms through weak bond interactions, thereby exhibit wide potentiality as medicinal drugs. So far, some coumarin-based drugs such as anticoagulant and antineurodegenerative agents have been extensively used in clinic. Coumarin-containing supramolecular medicinal agents as a new increasing expansion of supramolecular chemistry in pharmaceutical science have also been actively investigated in recent years. Coumarin-derived artificial ion receptors, fluorescent probes and biological stains are growing quickly and have a variety of potential applications in monitoring timely enzyme activity, complex biological events as well as accurate pharmacological and pharmacokinetic properties. This review provides a systematic summary and insight of the whole range of medicinal chemistry in the current developments of coumarin compounds as anticoagulant, antineurodegenerative, anticancer, antioxidative, antibacterial, antifungal, antiviral, antiparasitic, antiinflammatory and analgesic, antidiabetic, antidepressive and other bioactive agents as well as supramolecular medicinal drugs, diagnostic agents and pathologic probes, and biological stains. Some rational design strategies, structure-activity relationships and action mechanisms are discussed. The perspectives of the future development of coumarinbased medicinal chemistry are also presented.
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http://dx.doi.org/10.2174/1381612811319210013 | DOI Listing |
Acta Crystallogr E Crystallogr Commun
March 2025
Department of PG Studies and Research in Physics Albert Einstein Block UCS Tumkur University, Tumkur Karnataka-572103 India.
The title compound, CHNO, was synthesized by S2 reaction of bromo-methyl coumarin with 4,4-di-methyl-piperidine-2,6-dione. The mol-ecule crystalizes in the monoclinic system with space group 2/. The coumarin unit is almost planar with a dihedral angle between the aromatic rings of 0.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
March 2025
CRM2, CNRS-Université de Lorraine, Vandoeuvre-lès-Nancy CEDEX BP 70239, France.
In the title compound, CHBrO, the dihedral angle between the chromen-2-one ring system (r.m.s.
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
March 2025
Department of Physics, Faculty of Engineering and Natural Sciences, Manisa Celal Bayar University, TR-145140 Manisa, Turkey.
This paper explores the electronic structure and spectral characteristics of coumarin (C), C-6H, C-153, and C-343 in the protic polar solvent acetonitrile, combining computational methods via Density Functional Theory (DFT) and time-dependent Density Functional Theory (TD-DFT) with experimental analysis of UV-Vis and fluorescence spectra. The optoelectronic features of C, C-6H, C-153, and C-343 are primarily utilized in the solution phase for various applications, such as lasers and dye-sensitized solar cells. Computational studies were conducted using four different Modal Chemistry methods [MC1: CAM-B3LYP/6-311++G(d.
View Article and Find Full Text PDFChem Biodivers
March 2025
Shaanxi University of Chinese Medicine, college of pharmacy, , 712000, , CHINA.
Fraxinus species, with a long history of medicinal use, are diverse in type. All species that feature terminal inflorescences and exhibit a blue-purple fluorescence reaction under sunlight are considered to have medicinal value. However, only four species-Fraxinus rhynchophylla, Fraxinus chinensis, Fraxinus szaboana, and Fraxinus stylosa-are officially recognized in the Chinese Pharmacopoeia.
View Article and Find Full Text PDFJ Fluoresc
March 2025
College of Chemistry and Molecular Science, Henan University, Kaifeng, Henan, 475004, China.
Three novel coumarin-based arylpyrazolines were successfully designed and synthesized. Among them, probe B demonstrated excellent detection capabilities for Cu. According to the fluorescence titration and Job's plot, B could form a complex with Cu in a 2∶1 ratio, the detection limit was 1.
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