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  • Articles  (8)
  • 13C NMR  (4)
  • Food Science, Agricultural, Medicinal and Pharmaceutical Chemistry  (4)
  • Wiley-Blackwell  (8)
  • 1
    ISSN: 0749-1581
    Keywords: 13C NMR ; Diterpenes ; ent-Beyeranes ; ent-Beyer-15-enes ; Bicyclo[3.2.1]octanes ; Substituent effects ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A detailed analysis of the 13C NMR spectra of 39 isomeric ent-beyer-15-enes and ent-beyeranes functionalized at C-7, C-14, C-15 and C-16 has been performed. This diterpenic skeleton is a good example of a semirigid bicyclo[3.2.1]octane system. The sensitivity of 13C shielding to the stereochemical environment, particularly in polyfunctional compounds, has been confirmed. In some cases the ent-beyer-15-enes and ent-beyeranes show similar behaviour to that of similarly functionalized bicyclo[3.2.1]octane derivatives, but in other cases the shielding effects are very different. The compounds studied are a good model for the evaluation of shielding effects in exo/endo isomers of strained and rigid carbocyclic compounds.
    Additional Material: 12 Tab.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Archives of Insect Biochemistry and Physiology 17 (1991), S. 143-155 
    ISSN: 0739-4462
    Keywords: reproduction ; vitellin ; Hymenoptera ; caste ; Chemistry ; Food Science, Agricultural, Medicinal and Pharmaceutical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Vitellogenin has been identified in the ant Camponotus festinatus, both in queens and workers. In the workers, it is already present before adult eclosion in low concentrations (〈1 μg/μl hemolymph). Vitellogenin and vitellin are immunologically identical and are composed of a single type of apoprotein with an apparent Mr = 185,000. The molecular weight of the native molecules was estimated as ∼460,000 by pore limiting gradient electrophoresis. Vitellogenin was detected as a major protein in the hemolymph of young workers, both under queenright and queenless conditions. Thus, in spite of their sterility in the presence of the queen, C. festinatus workers are able to synthetize vitellogenin which is identical both in size and immunologically to the queen vitellogenin. About 6-7 weeks after adult eclosion, however, vitellogenin was usually undetectable in the hemolymph of queenright workers, particularly the minor workers, while it constituted about 30% of total protein in queenless workers. Protein concentration in the hemolymph of queenless insects increased up to 20-fold as compared to 1-day-old insects. Queenless workers also developed large amounts of perivisceral fat body, while queenright workers, particularly the minor workers, showed a dramatic fat body regression about 6 weeks after emergence.
    Additional Material: 7 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Archives of Insect Biochemistry and Physiology 9 (1988), S. 211-220 
    ISSN: 0739-4462
    Keywords: pheromone biosynthesis-activating neuropeptide ; calling behavior ; Lepidoptera ; Chemistry ; Food Science, Agricultural, Medicinal and Pharmaceutical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Adult females of Spodoptera littoralis (Lepidoptera: Noctuidae) showed a cyclic pattern of sex pheromone production, and high titers of (Z,E)-9,11-tetradecadienyl acetate, the major component of its pheromone blend, were only detected during scotophase. Maximal amounts of pheromone were extracted approximately 2 h into second scotophase. Decapitation before the beginning of darkness inhibited normal production of pheromone, and no calling behavior was observed. Injection of brain-suboesophageal ganglion (Br-SOG) homogenate at the onset of scotophase restored pheromone production in decapitated females to the levels characteristic of second scotophase. Pheromone biosynthesis was also stimulated in decapitated females during photophase. The response to Br-SOG homogenate injection was dose-dependent. The pheromonotropic activity of Br-SOG extract was the same when females were injected during photophase or scotophase.
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  • 4
    ISSN: 0739-4462
    Keywords: Bacillus thuringiensis ; Phthorimaea operculella ; insecticidal crystal protein ; receptors ; Chemistry ; Food Science, Agricultural, Medicinal and Pharmaceutical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The potato tuber moth is susceptible to at least three insecticidal crystal proteins (ICPs) from Bacillus thuringiensis: CrylA(b), CrylB, and CrylC. To design useful combinations of toxin genes either in transgenic plants or in new genetically modified B. thuringiensis strains, it is necessary to determine the binding characteristics of the different ICPs so as not to combine a pair sharing the same binding site. This has been accomplished using two different techniques: 125I-labeling of the ICPs with further measurement of the radioactivity bound to brush border membrane vesicles, and microscopic visualization of the bound ICPs by enzyme-linked reagents such as antibodies or streptavidin using biotinylated ICPs. Our results show that CrylA(b), CrylB, and CrylC bind to different sites in the brush border membrane of midgut epithelial cells. Also, the affinity of the binding sites for the ICPs and their concentration in brush border membrane vesicles has been determined in a laboratory strain and a storage collected population. No significant differences were found between these two strains. © 1994 Wiley-Liss, Inc.
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 28 (1990), S. 299-304 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Quipazines Substituted quinolines ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The complete assignment of the 13C NMR spectra of a series of biologically active quipazines substituted at position C-5, C-6 or C-7 of the quinoline moiety provides evidence for a strong conjugation between the π-electron cloud of the pyridine ring and the nitrogen lone pair of the piperazinyl residue. The SCS values of these quipazines are compared with those of the analogous quinolines, and their deviations are discussed in terms of conjugation effects.
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 28 (1990), S. 311-314 
    ISSN: 0749-1581
    Keywords: 13C NMR ; Substituent chemical shift values ; π bond orders ; Methoxy-substituted aromatic compounds ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The substituent chemical shift values induced by the methoxy group at the two ortho positions of aromatic compounds which include naphthalenes, quinolines, indoles, coumarins, flavones and benzofurans were linearly correlated with π-bond orders, affording the equation Δδortho(13C) = -98.68Pπ + 50.38 (correlation coefficient = 0.929; root mean square error = 1.95 ppm) when 40 pairs of values are considered. Elimination of six points corresponding to ring-junction quaternary carbons improves the correlation coefficient to 0.961 (root mean square error = 1.4 ppm) for the equation Δδortho(13C) = -126.85Pπ + 69.66.
    Additional Material: 1 Ill.
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  • 7
    ISSN: 0749-1581
    Keywords: NMR ; 13C NMR ; Chlorine isotope effect ; 13C chemical shifts ; para-Substituted chlorobenzenes ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: One-bond isotope shifts of 35Cl/37Cl natural abundance chlorine isotopomers were measured in the 75.4 MHz 13C NMR spectra of a series of para-substituted chlorobenzenes. The high-field isotope shift effect 1Δ13C(37Cl) was established from the relationship between the chlorine isotopomeric ratio and the carbon peak intensities. It was found that the 1Δ13C(37Cl) values are in the range of -4.0 to -5.2 ppb. The isotope shifts tend to decrease as the electron-attracting character of the substituent increases, providing a linear correlation between the isotope shift and the chemical shift of the chlorine-bearing carbon.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Archives of Insect Biochemistry and Physiology 6 (1987), S. 49-58 
    ISSN: 0739-4462
    Keywords: juvenile hormone ; vitellogenic oocytes ; yolk proteins ; Chemistry ; Food Science, Agricultural, Medicinal and Pharmaceutical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Using polyacrylamide gel electrophoresis (PAGE) under denaturing conditions, two major polypeptides of 200,000 and 170,000 daltons were detected in the hemolymph of mature female Oncopeltus fasciatus, but they were not found in the hemolymph of males or newly emerged females. Those polypeptides constituted the two major bands of early vitellogenic oocytes; however, they were absent from the yolk of mature eggs. The slower-migrating band (200,000 daltons) appears to correspond to a vitellogenic protein already identified in O. fasciatus, whose synthesis has been suggested to be independent of juvenile hormone (JH). Treatment of newly emerged adult females with the corpus allatum cytotoxin precocene II prevented the appearance of the female-specific bands and induced an important accumulation of other proteins in the hemolymph. Yolk deposition was also inhibited in those animals. Topical application of JH to precocene-treated females restored the appearance of the 200,000 and 170,000 dalton polypeptides in the hemolymph. These results suggest that JH is required for the synthesis of female-specific polypeptides in O. fasciatus.
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