Nuclear magnetic resonance spectroscopy of cobalt(II) porphyrin-quinone complexes. 1976

L Ford, and H A Hill, and B E Mann, and P J Sadler, and R J Williams

UI MeSH Term Description Entries
D008968 Molecular Conformation The characteristic three-dimensional shape of a molecule. Molecular Configuration,3D Molecular Structure,Configuration, Molecular,Molecular Structure, Three Dimensional,Three Dimensional Molecular Structure,3D Molecular Structures,Configurations, Molecular,Conformation, Molecular,Conformations, Molecular,Molecular Configurations,Molecular Conformations,Molecular Structure, 3D,Molecular Structures, 3D,Structure, 3D Molecular,Structures, 3D Molecular
D009285 Naphthoquinones Naphthalene rings which contain two ketone moieties in any position. They can be substituted in any position except at the ketone groups. Naphthalenediones,Naphthazarins,Naphthoquinone
D009682 Magnetic Resonance Spectroscopy Spectroscopic method of measuring the magnetic moment of elementary particles such as atomic nuclei, protons or electrons. It is employed in clinical applications such as NMR Tomography (MAGNETIC RESONANCE IMAGING). In Vivo NMR Spectroscopy,MR Spectroscopy,Magnetic Resonance,NMR Spectroscopy,NMR Spectroscopy, In Vivo,Nuclear Magnetic Resonance,Spectroscopy, Magnetic Resonance,Spectroscopy, NMR,Spectroscopy, Nuclear Magnetic Resonance,Magnetic Resonance Spectroscopies,Magnetic Resonance, Nuclear,NMR Spectroscopies,Resonance Spectroscopy, Magnetic,Resonance, Magnetic,Resonance, Nuclear Magnetic,Spectroscopies, NMR,Spectroscopy, MR
D011166 Porphyrins A group of compounds containing the porphin structure, four pyrrole rings connected by methine bridges in a cyclic configuration to which a variety of side chains are attached. The nature of the side chain is indicated by a prefix, as uroporphyrin, hematoporphyrin, etc. The porphyrins, in combination with iron, form the heme component in biologically significant compounds such as hemoglobin and myoglobin. Porphyrin
D011809 Quinones Hydrocarbon rings which contain two ketone moieties in any position. They can be substituted in any position except at the ketone groups.
D003035 Cobalt A trace element that is a component of vitamin B12. It has the atomic symbol Co, atomic number 27, and atomic weight 58.93. It is used in nuclear weapons, alloys, and pigments. Deficiency in animals leads to anemia; its excess in humans can lead to erythrocytosis. Cobalt-59,Cobalt 59
D001665 Binding Sites The parts of a macromolecule that directly participate in its specific combination with another molecule. Combining Site,Binding Site,Combining Sites,Site, Binding,Site, Combining,Sites, Binding,Sites, Combining
D014451 Ubiquinone A lipid-soluble benzoquinone which is involved in ELECTRON TRANSPORT in mitochondrial preparations. The compound occurs in the majority of aerobic organisms, from bacteria to higher plants and animals. Coenzyme Q
D014812 Vitamin K A lipid cofactor that is required for normal blood clotting. Several forms of vitamin K have been identified: VITAMIN K 1 (phytomenadione) derived from plants, VITAMIN K 2 (menaquinone) from bacteria, and synthetic naphthoquinone provitamins, VITAMIN K 3 (menadione). Vitamin K 3 provitamins, after being alkylated in vivo, exhibit the antifibrinolytic activity of vitamin K. Green leafy vegetables, liver, cheese, butter, and egg yolk are good sources of vitamin K.

Related Publications

L Ford, and H A Hill, and B E Mann, and P J Sadler, and R J Williams
June 1980, The Biochemical journal,
L Ford, and H A Hill, and B E Mann, and P J Sadler, and R J Williams
March 1973, Journal of the American Chemical Society,
L Ford, and H A Hill, and B E Mann, and P J Sadler, and R J Williams
August 1986, Zeitschrift fur Kardiologie,
L Ford, and H A Hill, and B E Mann, and P J Sadler, and R J Williams
June 1990, Analytical chemistry,
L Ford, and H A Hill, and B E Mann, and P J Sadler, and R J Williams
June 1988, Analytical chemistry,
L Ford, and H A Hill, and B E Mann, and P J Sadler, and R J Williams
September 1995, Academic radiology,
L Ford, and H A Hill, and B E Mann, and P J Sadler, and R J Williams
July 1986, Scottish medical journal,
L Ford, and H A Hill, and B E Mann, and P J Sadler, and R J Williams
June 1995, Analytical chemistry,
L Ford, and H A Hill, and B E Mann, and P J Sadler, and R J Williams
September 1988, British journal of hospital medicine,
L Ford, and H A Hill, and B E Mann, and P J Sadler, and R J Williams
May 1977, Journal of the American Chemical Society,
Copied contents to your clipboard!