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  • 11
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 12 (1982), S. 321-329 
    ISSN: 1572-8854
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The title compound is orthorhombic, space groupP212121,a=15.992(9),b=15.693(9),c=11.205(6) Å,Z=4. The structure was solved from diffractometer data by direct methods, and refined toR 0.085 for 1216 observed (of a total of 2421) reflections. Strain in the almost planar ringA is indicated by the endocyclic torsion angles, ringsB andC, which aretrans fused and chair-shaped, while ringD is intermediate between a 13β-envelope and a 13β, 14α-half-chair conformation. RingE, a 2,5,6-trisubstituted 1,3-dioxane-like unit, adopts a highly distorted boat conformation. The bending of the skeleton is toward itsα side. TheA-ring carbonyl substituent accepts one hydrogen bond involving a symmetry-related 11β-ol function [O(1)-O(2) 2.81, O(2)-H 1.0, H---O(1) 1.8 Å/ O(2)-H---O(1) 165°].
    Type of Medium: Electronic Resource
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  • 12
    ISSN: 1572-8854
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The crystal structure of noxiptyline hydrochloride C19H23N 2 + OCl− (5-dimethylaminoethyloximino-5H-dibenzo[a,d]cyclohepta-1,4-diene hydrochloride), is monoclinic:P21/c, a=15.894(5),b=9.116(2),c=13.755(4) Å,β=113.00(7)°,Z=4. It has been determined by application of a multisolution direct method procedure, and refined by full-matrix least squares to a conventionalR of 0.056 for 1674 counterreflections (to 2Θ=44°, MoKα radiation). The noxiptyline molecule adopts a folded boat conformation with dihedral angle between benzo-group planes of 129.3°, and the atypical dimethylaminoethyloximino side chain adopts agauche-gauche distribution about the O-Cβ and Cα-Cβ bonds. The only intermolecular approach less than van der Waals distances is the hydrogen bond between the amine nitrogen atom and the chloride ion.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 13 (1983), S. 293-301 
    ISSN: 1572-8854
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The structure of the title compound (C22 H20O2S) is orthorhombic with space groupPca21,a=15.467(8),b=9.410(6),c=25.092(7) Å andZ=8. It has been solved by direct methods and refined by full-matrix least-squares techniques (phenyl rings as rigid bodies) to a conventionalR factor of 0.088 for 1056 reflections. There are only minor differences in the geometry of the two crystallographically nonequivalent molecules. The center ring of the molecule adopts a folded-boat conformation, with a very small angle (106°) between the two benzo-group planes of the (6,7,6) system.
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  • 14
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 20 (1990), S. 621-624 
    ISSN: 1572-8854
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 21 (1991), S. 419-429 
    ISSN: 1572-8854
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The conformational features of three tetrahydropyridinyl oxime cognition activators 1-(1-methyl-1,2,5,6-tetrahydro-3-pyridinyl)ethanone oxime·HCl (I), 1-(1-methyl-1,2,3,6-tetrahydro-4-pyridinyl)ethanone oxime·HCl (II), and 1-(1,2,5,6-tetrahydro-3-pyridinyl)ethanone O-methyloxime HCl(III) were analyzed by X-ray diffraction and the quantum mechanical semiempirical PM3 methods. Results indicate that in the solid state the drugs exhibit “anti-syn” isomerism, with the substituent at the oxime oxygen atomanti oriented in respect to C=N. This arrangement also represents a low-energy situationin vacuo, as confirmed at the PM3 level, although another low-energy conformation (“clinal-anti”) could be of significance in the conformational energetics of the drugs.
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  • 16
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical crystallography 21 (1991), S. 567-574 
    ISSN: 1572-8854
    Source: Springer Online Journal Archives 1860-2000
    Topics: Geosciences , Physics
    Notes: Abstract The molecular structures of the cognition activators (±)1-benzenesulphonyl-2-oxo-5-ethylthiopyrrolidine (1) and (±)1-benzenesulphonyl-2-oxo-5-isopropylthiopyrrolidine (2) were determined by means of X-ray diffraction and semi-empirical quantum mechanical methods. The conformational properties of the compounds, in the solid state andin vacuo (free molecule), were compared with those of the corresponding oxygenated derivatives bearing, in position 5, ethoxy and isopropyloxy substituents, respectively. The molecular arrangements of (1) and (2) in the solid state are similar, with the exception of the side chain on C(5), and they are retained alsoin vacuo. Both present an “envelope” conformation of the five-membered ring, and the relative positions of the five- and six-membered rings look similar and parallel those of their oxygenated parents. Fromin vacuo calculations another low-energy arrangement seems to be possible, and a detailed examination of the side-chain freedom in (1) and (2) gives more insight in the conformational properties of the compounds.
    Type of Medium: Electronic Resource
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  • 17
    ISSN: 1432-0843
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Tumor-tissue platinum levels and major pharmacokinetic parameters were determined in 11 patients with head and neck squamous cancer (HNSC) who were given cisplatin (50 mg/m2 daily x 2 days) and 5-fluorouracil (5-FU; 1000 mg/m2, continuous infusion x 5 days) either i.a. or i.v. The plasma peak platinum concentrations (c max) and the areas under the curve for total platinum concentration versus time (AUC) during i.a. infusions were lower than the i.v.c max (mean, 1.92±0.28 and 4.08±2.80 mg/l, for i.a. and i.v. infusions, respectively) and AUC values (mean, 22.55±4.96 and 40.66±10.71 mg h−1 l−1 for i.a. and i.v. treatment, respectively), suggesting a first-passage extraction of the drug by the tumor mass during i.a. infusion. However, no statistically significant difference was found in platinum tumor concentrations after i.a. administration versus i.v. infusion. The lack of a difference in tumor platinum concentrations between the i.a. and the i.v. administration routes might be explained either by a relatively high blood supply to the tumor area, enabling efflux of the surplus free platinum from the tissue, or by the delay between drug infusion and biopsy. After three cycles of i.a. treatment good tumor remission was obtained with minimal local toxicity. Larger clinical studies testing the advantages of the i.a. administration route over i.v. infusion appear to be necessary.
    Type of Medium: Electronic Resource
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  • 18
    ISSN: 1572-901X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The reactions of the tridentate Schiff base ligandN-(2-hydroxyphenyl) salicylideneimine (HOPhsalH) with oxotetrachlororhenate (IV) have been investigated. The complexes (Bu4N)[ReOCl3(HOPhsal)], (Bu4N)[ReOCl2(OPhsal)],cis- [ReOCl(MeOH)(OPhsal)],trans-[ReOCl(MeOH)(OPhsal)] (1), trans-[ReOCl(OH2)(OPhsal)] · Et2O (2), trans-[ReOCl(OH2)(OPhsal)] · Me2CO,cis-[ReOCl(PPh3)(OPhsal)],cis-[ReOCl(PMe2Ph)(OPhsal)](3) have been synthesized and characterized. The crystal structures of(1), (2) and(3) have been solved from three-dimensional x-ray data by Patterson and Fourier methods and refined by least-squares methods to R 0.10 for(1), 0.042 for(2) and 0.059 for(3). In all the three complexes, the ligands surrounding the rhenium atom are at the apices of a distorted octahedron, with the equatorial ONO donor atoms of the tridentate Schiff base bent away from the Ooxo and toward the loosely bound MeOH in(1), H2O in(2) and Cl in(t3). The fourth equatorial substituent is Cl (1 and2) and PMe2Ph(3) and the rhenium atoms lie 0.30–0.37 Å above the best plane through the four equatorial atoms, in the direction of the Ooxo. All interatomic distances and angles are normal.
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  • 19
    ISSN: 1432-1424
    Keywords: outer mitochondrial membrane ; channel ; VDAC ; planar bilayer ; patch clamp ; aluminum
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary Detergent-free rat brain outer mitochondrial membranes were incorporated in planar lipid bilayers in the presence of an osmotic gradient, and studied at high (1 m KCl) and low (150 mm KCl) ionic strength solutions. By comparison, the main outer mitochondrial membrane protein, VDAC, extracted from rat liver with Triton X-100, was also studied in 150 mm KCl. In 1 m KCl, brain outer membranes gave rise to electrical patterns which resembled very closely those widely described for detergent-extracted VDAC, with transitions to several subconducting states upon increase of the potential difference, and sensitivity to polyanion. The potential dependence of the conductance of the outer membrane, however, was steeper and the extent of closure higher than that observed previously for rat brain VDAC. In 150 mm KCl, bilayers containing only one channel had a conductance of 700 ± 23 pS for rat brain outer membranes, and 890 ± 29 pS for rat liver VDAC. Use of a fast time resolution setup allowed demonstration of open-close transitions in the millisecond range, which were independent of the salt concentration and of the protein origin. We also found that a potential difference higher than approx. ± 60 mV induced an almost irreversible decrease of the single channel conductance to few percentages of the full open state and a change in the ionic selectivity. These results show that the behavior of the outer mitochondrial membrane in planar bilayers is close to that detected with the patch clamp (Moran et al., 1992, Eur. Biophys. J. 20:311–319). The neurotoxicological action of aluminum was studied in single outer membrane channels from rat brain mitochondria. We found that μm concentrations of Al Cl3 and aluminum lactate decreased the conductance by about 50%, when the applied potential difference was positive relative to the side of the metal addition.
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  • 20
    ISSN: 1572-901X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The electrochemical behaviour of a series of cationic platinum(II) isocyanide complexes has been studied in acetonitrile. All the tested compounds are oxidized at a platinum electrode via a two-electron process and reduced at a platinum or mercury electrode via two successive one-electron steps. The anodic step involves the formation of platinum(IV) complexes. The main reduction product formed in correspondence to the first cathodic process is a stable dimer platinum(I) containing bridging isocyanide ligands. Platinum(0) species are formed in the subsequent reduction step.
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