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  • Inorganic Chemistry  (19)
  • Nuclear reactions  (3)
  • 13.75.Cs  (2)
  • Endothelial cells  (2)
  • 1
    ISSN: 0375-9474
    Keywords: Nuclear reactions
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Nuclear Physics, Section A 173 (1971), S. 449-455 
    ISSN: 0375-9474
    Keywords: Nuclear reactions
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Nuclear Physics, Section A 103 (1967), S. 238-240 
    ISSN: 0375-9474
    Keywords: Nuclear reactions
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-1912
    Keywords: Key words 5-Hydroxytryptamine (5-HT ; serotonin) ; 5-HT1D receptors ; 5-HT1Dβ receptors ; Endothelial cells ; Cyclic AMP
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Pharmacological evidence has suggested the presence of 5-hydroxytryptamine (5-HT, serotonin), 5-HT1D receptors on endothelial cells but these receptors have never been identified unambiguously on this type of cells. We now report that human umbilical vein endothelial cells (HUVEC) express 5-HT1D receptors coupled to inhibition of cyclic AMP formation. 5-HT and the 5-HT1D receptor agonists 5-carboxamidotryptamine (5-CT) and sumatriptan were approximately equipotent at inhibiting forskolin-stimulated cyclic AMP accumulation in HUVEC (mean pEC50 7.6–8.2, maximal effect 30% inhibition). The 5-HT1A receptor agonist, 8-OH-DPAT was clearly less potent (pEC50 6.2) and less efficacious. The selective 5-HT1D receptor antagonist, GR127935 (1 nM) markedly inhibited the effect of 5-HT (apparent pKB 10.8). Reverse transcription-polymerase chain reaction analysis showed the mRNA for 5-HT1Dβ receptors to be expressed in HUVEC. These results demonstrate the presence of functional 5-HT1D receptors and the expression of 5-HT1Dβ receptor mRNA in HUVEC. They support the involvement of 5-HT1Dβ receptors in endothelial-mediated responses to 5-HT.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-1912
    Keywords: 5-Hydroxytryptamine (5-HT, serotonin) ; 5-HT1D receptors ; 5-HT1Dβ receptors ; Endothelial cells ; Cyclic AMP
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Pharmacological evidence has suggested the presence of 5-hydroxytryptamine (5-HT, serotonin), 5-HT1D receptors on endothelial cells but these receptors have never been identified unamiguously on this type of cells. We now report that human umbilical vein endothelial cells (HUVEC) express 5-HT1D receptors coupled to inhibitiion of cyclic AMP formatin. 5-HT and the 5-HT1D receptor agaonists 5-carboxamidotryptamine (5-CT) and sumatriptan were approximately equipotent at inhibiting forskolin-stimulated cyclic AMP accumulation in HUVEC (mean pEC50 7.6–8.2, maximal effect 30% inhibition). The 5-HT1A receptor agonist, 8-OH-DPAT was clearly less potent (pEC50 6.2) and less efficacious. The selective 5-HT1D receptor antagonist, GR127935 (1 nM) markedly inhibited the effct pf 5-HT (apparent pKB 10.8). Reverse transcription-polymerase chain reaction analysis showed the mRNA for 5-HT1Dβ receptors to be expressed in HUVEC. These results demonstrate the presence of functional 5-HT1D receptors and the expression of 5-HT1Dβreceptor mRNA in HUVEC. They support he involvement of 5-HT1Dβ receptors in endothelial-mediated responses to 5-HT.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1434-601X
    Keywords: 36.10.Gv ; 13.75.Cs
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The yields of the atomic 4→3 transitions in antiprotonic14N,16,17,18O,19F, and23Na were measured at the CERN antiproton facility, LEAR. From these, the widths Γup of the 4f levels were determined to be 136±19meV (14N); 603±22 meV (16O); 731±35 meV (17O); 795±23 meV (18O); 2.79±0.16 eV (19F); and 23.8±7.4 eV (23Na).
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1434-601X
    Keywords: 36.10.Gv ; 13.75.Cs
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract The strong ¯p-nucleus spin-orbit interaction was investigated in a measurement of the strong-interaction effects of the 9→8 transition in ¯p 174Yb at the Low-Energy Antiproton Ring (LEAR) at CERN. This measurement was part of an experimental programme where, for the first time, the fine-structure components of the last observable X-ray transition in a ¯p atom, which carries information on the strong ¯p-nucleus interaction, were resolved and studied individually. The observed splitting ΔE exp=2408±26 eV consists of the electromagnetic fine-structure splitting ΔE FS=2350 eV and an additional splitting Δɛ=58±26 eV. In addition, one finds a significant difference in the level widths of Δ=195±59 eV with the larger value⇊=1216±41 eV for the lower fine-structure level. This experiment follows an earlier measurement on ¯p 138Ba, where the transition 8→7 is influenced by the strong interaction. In this case, however, the fine-structure components could not be resolved. The results for174Yb may be attributed to a spin-orbit (LS) term in the complex strong-interaction potential.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 586 (1990), S. 141-148 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation and Crystal Structure of CrSO4 · 3 H2OEvaporating a solution of Cr2+ in dilute sulphuric acid at 70°C light blue crystals of CrSO4 · 3 H2O were grown. Its x-ray powder diffraction pattern is quite similar to that of CuSO4 · 3 H2O. The crystal structure refinement of CrSO4 · 3 H2O (space group Ce, a = 5.7056(8) Å, b = 13.211(2) Å, c = 7.485(1) Å, β = 96.73(1)°, Z = 4) from single crystal data, using the parameters of the copper compound as starting values, results in a final R-value of R = 3.8%.The surrounding of the Cr2+ ion can be described as a strongly elongated octahedron. The basal plane of the CrO6-octahedron consists of three hydrate oxygen atoms and one sulphate oxygen atom. The two more distant axial oxygen atoms also belong to sulphate groups. Thus they are forming chains of alterning CrO6-octahedra and SO4-tetrahedra along [110] and [1-10] linked via common corners. These chains are connected via sulphate groups and by bridging hydrogen bonds to a 3-dimensional network.
    Notes: Durch Kristallisieren aus einer schwefelsauren Lösung von Chrom(II)-Sulfat (T ≈ 70°C) ist das hellblaue Trihydrat CrSO4 · 3 H2O erhältlich. Die Verbindung ist isotyp zu CuSO4 · 3 H2O. Die Strukturverfeinerung anhand von Einkristalldaten erfolgte in der Raumgruppe Cc mit a = 5,7056(8) Å, b = 13,211(2) Å, c = 7,485(1) Å, β = 96,73(1)°, Z = 4 und konvergierte bei R = 3,8%.Cr2+ ist verzerrt oktaedrisch koordiniert. Die Basisfläche des Oktaeders wird von drei Hydratsauerstoffatomen und einem Sulfatsauerstoffatom aufgespannt. Zwei weitere Sauerstoffatome von Sulfatgruppen vervollständigen in einem größeren Abstand die elongierten Oktaeder. Diese sind untereinander über gemeinsame Sulfatpolyeder verknüpft. Dadurch ergeben sich Ketten, in denen CrO6-Oktaeder und SO4-Tetraeder abwechseln. Diese Ketten, deren Orientierung jeweils [110] und [1-10] in c-Richtung wechselt, sind über Sulfatgruppen und Wasserstoffbrückenbindungen miteinander verbunden.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 580 (1990), S. 224-224 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 349 (1967), S. 158-163 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The isotopic exchange of Cl- with trans-[Co(en)2, Cl2*]+ and of Br- with trans-[Co(en), Br2*]+ in acid methanolic solutions and its dependence upon temperature (30 bis 60°C ), complex salt-, halide- and acid concentration have been investigated. For trans-[Co(en)2Cl2*]+ in 0.51 N methanolic HCl a reaction velocity k1 (40°C) = 0.53 · 10-3 min-1 and an activation energy EA = 24 kcals./mole have been found, for trans-[Co(en), Br2*]+ in 0.25 N methanolic HBr k1 (40°C) = 3.9 · 10-3 min-1 and EA = 20.0 kcals./mole. From the experimental results the intermediate occurrence of a metastable solvate complex is concluded. The formation of ion pairs at increasing halide ion concentration accelerates the reaction.
    Notes: Der Isotopenaustausch von trans-[Co(en)2, Cl2*]+ mit Cl--Ionen und von trans-[Co(en)2Br2*]+ mit Br--Ionen wurde in sauren, methanolischen Lösungen in Abhängigkeit von der Temperatur (30-60°C), der Komplexsalz-, der Wasserstoffionen- und der Halogenionenkonzentration untersucht (1). Für trans-[Co(en)2, Cl2*]+ wurde in 0,51 n methanolischer HCl k1 (40°C) = 0,53 · 10-3 min-1 und eine Aktivierungsenergie EA von 24 kcal/Mol gefunden, für trans-[Co(en)2, Br2*]+ in 0,25 n methanolischer HBr k1 (40°C) = 3,9 · 10-3 · min-1 und EA = 20,0 kcal/Mol. Es wird auf das Vorliegen eines metastabilen Solvatkomplexes als Übergangszustand geschlossen. Die Bildung von Ionenpaaren mit steigender Halogenionenkonzentration beschleunigt die Reaktion.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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