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  • 1
    ISSN: 0014-5793
    Keywords: Human cerebellum ; Neopterin ; Nitric oxide synthase ; Tetrahydrobiopterin
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0014-5793
    Keywords: FAD ; FMN ; L-Arginine ; Nitric oxide ; Reaction mechanism ; Tetrahydrobiopterin
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    FEBS Letters 277 (1990), S. 215-219 
    ISSN: 0014-5793
    Keywords: Ca^2^+ ; Calmodulin ; Guanylyl cyclase ; NADPH ; Nitric oxide synthase ; Tetrahydrobiopterin
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 351 (1995), S. 453-463 
    ISSN: 1432-1912
    Keywords: Key wordsNitric oxide synthase ; Tetrahydrobiopterin ; Pteridine metabolism
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract (6R)-5,6,7,8-Tetrahydro-L-biopterin (H4biopterin) is well known as a cofactor of enzymes that hydroxylate aromatic amino acids. More recent work has revealed an essential role of H4biopterin in the biosynthesis of nitric oxide (NO), an intercellular messenger molecule synthesized from L-arginine by different NO synthase isozymes in many species and tissues. While the function of H4biopterin in aromatic amino acid hydroxylation is well established, the role of this pteridine in NO synthesis is, as yet, elusive. Current experimental evidence hints at a dual mode of action of H4biopterin, involving both an allosteric effect on the NO synthase protein and participation as a reactant in L-arginine oxidation. As discussed in detail in the present article, the latter effect of this pteridine may be related to the protection of NO synthase from feedback inhibition by NO.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 607 (1992), S. 26-28 
    ISSN: 0044-2313
    Keywords: Tetrakis(di-tert.-butylphosphino)diphosphane ; [(tBu)2P]2P—P[P(tBu)2]2 ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Crystal Structure of Tetrakis(di-tert.-butylphosphino)diphosphane [(tBu)2P]2P—P[P(tBu)2]2[(tBu)2P]2P—P[P(tBu)2]2 1 obtained at -20°C from a solution of (tBu)2P—P=P(Br)tBu2 forms yellow crystals (regular hexagons). 1 crystallizes monoclinic in the space group C2/c with a = 2145.6pm, b = 1137pm, c = 1696.1pm, β = 110.075° and Z = 4 formula units in the elementary cell. Due to high steric load the bond angles at the tertiary P atoms with δ = 115.7° are significantly larger than those at the primary P atoms with δ = 108.6°.
    Notes: [(tBu)2P]2P—P[P(tBu)2]2 1 sich aus (tBu)2P—P(Br)tBu2 (toluolische Lösung, -20°C) und fällt als gelbe Kristalle (regelmäßige Sechsecke) aus. 1 kristallisiert monoklin in der Raumgruppe C2/c mit den Gitterkonstanten a = 2145,6pm, b = 1137pm, c = 1696pm, β = 110,75°. Die Elementarzelle enthält 4 Formeleinheiten. Die Bindungswinkel an den tertiären P-Atomen mit δ = 115,7° sind infolge der hohen sterischen Belastung der tert. P-Atome gegenüber denen an den primären P-Atomen mit δ = 108,6° deutlich aufgeweitet.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 602 (1991), S. 73-78 
    ISSN: 0044-2313
    Keywords: 1,2,3,4-Tetrakis(di-tert-butylphosphanyl)-cyclo-tetraphosphane ; 31P n.m.r. ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Cyclotetraphosphane P4[P(tBu)2]4P4[P(tBu)2]4 1 is obtained by thermal decomposition (20°C) of (tBu)2P—P = P(tBu)2Br which is formed from [(tBu)2P]2PLi and 1,2-dibromoethane. The 31P NMR spectrum of 1 shows two complex signal patterns of the AA′ A″ A‴ XX′X″X‴ type; δ = +63 ppm (exocyclic) and δ = -43 ppm (cyclic).1 crystallizes monoclinic in the space group C2/c, (a = 2240.8(17) pm, b = 885.6(7) pm, c = 2221.8(14) pm, β = 101.72(5)°) with Z = 4 molecules in the elementary cell. The molecule has E conformation. The four-membered ring is folded (dieder angle 61°) to give the P(tBu)2 groups nearly equatorial and the lone pairs nearly axial positions.
    Notes: P4[P(tBu)2]4 1 entsteht bei der thermischen Zersetzung des (tBu)2P—P = P(tBu)2Br bei 20°C, das sich aus [(tBu)2P]2PLi und 1,2-Dibromethan bildet. Das 31P-NMR-Spektrum von 1 enthält zwei komplexe Signalgruppen; δ = +63 ppm (exocyclisch) und δ = -43 ppm (cyclisch). Es liegt ein AA′ A″ A‴ XX′X″X‴ Spinsystem vor. 1 kristallisiert monoklin in der Raumgruppe C2/c, a = 2240,8(17) pm, b = 885,6(7) pm, c = 2221,8(14) pm, β = 101,72(5)° mit Z = 4 Molekülen in der Elementarzelle. Das Molekül besitzt E-Konformation. Der Vierring ist gefaltet, Diederwinkel 61°. Dadurch nähern sich die P(tBu)2-Gruppen einer äquatorialen und die nichtbindenden Elektronenpaare am Phosphor einer axialen Position.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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