Adenine had a concentration-dependent relaxation action on the phenylephrine-contracted aorta ring, with an EC(50) value of 0.40±0.12 mM. This effect was also observed in the endothelium-denuded aorta. Among the adenine analogues, N-methyladenine and benzimidazole still evoked an apparent relaxation effect, while 1-, 3- or 7-methyladenine and imidazole were no longer vasodilators. These findings demonstrate that the imino group from the uncharged imidazolium moiety in adenine played a key role in the relaxation of the contracted aorta.
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http://dx.doi.org/10.1271/bbb.110806 | DOI Listing |
Macromolecules
May 2024
Grupo de Nanomateriais, Fotónica e Materia Branda, Departamento de Física de Partículas, Universidade de Santiago de Compostela, Campus Vida s/n, E-15782 Santiago de Compostela, Spain.
Polymer-based solid-like gel electrolytes have emerged as a promising alternative to improve battery performance. However, there is a scarcity of studies on the behavior of these media at the electrochemical interface. In this work, we report classical MD simulations of ternary polymer electrolytes composed of poly(ethylene oxide), a lithium salt [lithium bis(trifluoromethanesulfonyl)imide], and different ionic liquids [1-butyl-1-methylpyrrolidinium bis(trifluoromethanesulfonyl)imide and 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide] confined between two charged and uncharged graphene-like surfaces.
View Article and Find Full Text PDFLangmuir
May 2024
Institute of Particle Technology, Department of Chemical and Biological Engineering, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Cauerstr. 4, 91058 Erlangen, Germany.
In this study, we systematically analyze the surface tension and Hansen solubility parameters (HSPs) of imidazolium-based ionic liquids (ILs) with different anions ([NTf], [PF], [I], and [Br]). These anions are combined with the classical 1-alkyl-3-methyl-substituted imidazolium cations ([CCIm]) and a group of oligoether-functionalized imidazolium cations ([(mPEG)Im]) based on methylated polyethylene glycol (mPEG). In detail, the influences of the length of the alkyl- and the mPEG-chain, the anion size, and the water content are investigated experimentally.
View Article and Find Full Text PDFJ Phys Chem B
August 2021
N.N. Semenov Federal Research Center for Chemical Physics, Russian Academy of Science, Kosygin St. 4, Moscow 119991, Russia.
The rotational and translational diffusion of negatively charged and uncharged spin probes in five imidazolium-based room-temperature ionic liquids (RTILs), 1-ethyl-3-methylimidazolium tetrafluoroborate, emimBF, 1-butyl-3-methylimidazolium tetrafluoroborate, bmimBF, 1-octyl-3-methylimidazolium tetrafluoroborate, omimBF, 1-octyl-3-methylimidazolium hexafluorophosphate, omimPF, and 1-octyl-3-methylimidazolium chloride, omimCl, has been studied by means of electron paramagnetic resonance spectroscopy. Detailed analyses of the spin-Hamiltonian parameters and spin exchange interactions have been carried out. The temperature dependences of the line broadening induced by the electronic dipole-dipole interaction and the electron spin exchange coupling are determined.
View Article and Find Full Text PDFACS Macro Lett
January 2020
Department of Chemistry, University of Colorado, Boulder, Colorado 80309, United States.
Direct, living ring-opening metathesis polymerization of a highly paramagnetic, norbornene-based imidazolium FeCl ionic liquid monomer was achieved using the Grubbs third-generation catalyst and starting the polymerization off with an uncharged, nonparamagnetic norbornene monomer in a sequential block copolymerization. Preparing the paramagnetic norbornene imidazolium FeCl monomer in high purity was found to be crucial for enabling living polymerization behavior and generating paramagnetic diblock copolymers with predictable block lengths and compositions.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
March 2020
Georg-August Universität Göttingen, Institut für Organische und Biomolekulare Chemie, Tammannstr. 2, 37077, Göttingen, Germany.
We report a new class of stable mesoionic N-heterocyclic olefins, featuring a highly polarized (strongly ylidic) double bond. The ground-state structure cannot be described through an uncharged mesomeric Lewis-structure, thereby structurally distinguishing them from traditional N-heterocyclic olefins (NHOs). mNHOs can easily be obtained through deprotonation of the corresponding methylated N,N'-diaryl-1,2,3-triazolium and N,N'-diaryl-imidazolium salts, respectively.
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