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  • 1980-1984  (10)
  • 1940-1944
  • Analytical Chemistry and Spectroscopy  (8)
  • Cell & Developmental Biology  (2)
  • 1
    Electronic Resource
    Electronic Resource
    New York, N.Y. : Wiley-Blackwell
    Journal of Cellular Biochemistry 20 (1982), S. 71-80 
    ISSN: 0730-2312
    Keywords: aminoglycoside ; fluorescent paromomycin ; human fibroblasts ; lysosomes ; endocytosis ; exocytosis ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Human fetal lung fibroblasts grown in the presence of dansyl-paromomycin (DNS-Pm), a fluorescent derivative of the aminoglycoside antibiotic, paromomycin, probably accumulate DNS-Pm in the lysosomes. The intracellular concentration of DNS-Pm is proportional to the extracellular concentration and to the length of time cells are exposed to the compound. The accumulation of DNS-Pm by human fibroblasts continued to increase for several days, reaching a saturation after 7 days. The kinetic data are consistent with the establishment of a steady state in the cell between fluid-phase pinocytosis and exocytosis of DNS-Pm. About 80% of the intracellular DNS-Pm was released in 24 hr when fresh medium without the analogue was added. The residual 20% remained within the cells, suggesting that it may be irreversibly bound to the lysosomes, endoplasmic reticulum, or ribosonius. The uptake of paromomycin by cells in culture may be a useful means to study error propagation during growth and lifespan of cells in vitro.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    The @Anatomical Record 210 (1984), S. 463-475 
    ISSN: 0003-276X
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: Uteri from hibernating bats, Myotis lucifugus, collected periodically from Renfrew County, Ontario, were fixed in 2% glutaraldehyde and processed for electron microscopy or incubated in glyoxylic acid to show adrenergic nerves by fluorescence. The bat uterus is structurally typical of mammalian species; although the right uterine horn is permanently enlarged in parous bats due to hypertrophy of both myometrium and endometrium. Nerves were abundant between both longitudinal and circular layers of muscle cells. Unmyelinated, and some myelinated, axons, ranging from few to many, coursed generally parallel to the uterine long axis. Numerous axonal varicosities containing small dense-cored (adrenergic) vesicles or, less often, small agranular (cholinergic) vesicles, were found forming close nerve-muscle contacts between myometrial cells and blood vessels. Fluorescent microscopy showed a dense network of adrenergic nerves in parous uteri, but a sparse network in nulliparous uteri. A specific adrenergic nerve marker, 5-hydroxydopamine, greatly increased the density and in some instances, the size of granular vesicles, while 6-hydroxydopamine, which depletes adrenergic neutrotransmitter, reduced the number of dense-cored vesicles. Nulliparous uteri appeared unchanged by six daily injections of 0.1 μg estradiol-17β; 0.25 mg progesterone, or both; but parous uteri were greatly enlarged by all regimes. Nerve ultrastructure, however, appeared unaffected by steroid treatment; nor, despite the absolute dextral bias in implantation, were left-right differences observed. Gap junctions were not found between muscle cells in myometria of any bat uteri. Based on this study, we suggest that M. lucifugus may provide a most useful model for examination of neurogenic regulation of the uterus.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 13 (1980), S. 293-298 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of thirteen 15N-enriched N-aryl imines derived from benzaldehydes and acetophenones have been prepared and examined by 13C and 1H NMR. Preferred conformations of the C-arvl and N-aryl rings have been deduced from 13C chemical shifts and 13C-15N couplings. Evidence for steric inhibition of resonance in O-alkylated materials is presented. Relative signs of 1J(CN) and 2J(CCN) have been determined in some compounds. An E: Z interconversion barrier of 21.6 kcal mol-1 has been obtained from 1H NMR coalescence data.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 16 (1981), S. 156-159 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Carbon-13 NMR chemical shifts are reported for nine tricyclic aromatic ketones formally derived from indanone. The influences of remote ring size, as well as linear, angular exo and angular endo ketone orientation are examined. Results are compared with available 1H NMR data. For indanone itself, based on selective 1H decoupling experiments, a recently reported CIDNP derived 13C signal assignment is shown to be in error.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 19 (1982), S. 98-101 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C NMR chemical shifts and 13C—31P couplings are reported for triphenyl phosphate and 13 alkyl derivatives. In ortho-alkylated materials, it is found that the upfield γ shielding effect is only operative when the carbon atom, situated γ to the exocyclic oxygen, bears at least one hydrogen. Conformational changes about the aryl—O bond can be monitored via the vicinal 31p—O—C—13C couplings.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A novel, computer aided approach to the interpretation of mass spectra is documented by its application to a series of recently isolated marine sterols. The method consists of construction of biosynthetically plausible candidate structures, prediction of their major mass spectral fragmentation paths using class-specific rules derived from a training set of known compounds, and a system of ranking candidate structures based on a comparison of the predicted and observed spectra.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 14 (1980), S. 517-521 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C NMR chemical shifts and 13C—31P couplings are reported for ten arylphosphoramidates and five arylphoshorimidates. The para-carbon chemical shifts in the phosphoramidates are interpreted in terms of substantial nitrogen lone pair delocalization into the aromatic ring, a phenomenon which is subject to steric inhibition of resonance. By contrast, in the phosphorimidates the electron release into the phenyl ring is not attenuated by steric congestion. Conformational changes about the aryl—N bond in all compounds have been monitored by vicinal 31P—N—C—13C couplings.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A number of isomeric polycyclic aromatic hydrocarbons may be distinguished using electron capture negative chemical ionization when methane is used as a buffer gas, including benzo[a]pyrene and benzo[e]pyrene. The ionization behavior of these compounds may be predicted, on the basis of their electron afinities, allowing compounds to be distinguished without the use of standards.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 21 (1983), S. 436-442 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C NMR chemical shifts and 13C—31P couplings are reported for 18 phosphol-3-ene 1-oxides and 18 corresponding sulfides. The effects of methyl substitution at positions 3 and 4 on the carbon shifts have been systematically explored and substituent parameters derived. One bond couplings from phosphorus to C-2 and C-5 have been related to the sum of the exocyclic substituent group electronegativities (covalent boundary potential values).
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 22 (1984), S. 127-128 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 13C and 15N NMR chemical shifts and 13C-31P and 15N-31P coupling contants are reported for a series of ten 4-substituted-1-dimethylphosphonopiperazines.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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