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  • Chemistry  (14)
  • Renal tubule  (2)
  • 1975-1979  (10)
  • 1935-1939  (6)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 371 (1977), S. 141-145 
    ISSN: 1432-2013
    Keywords: Renal tubule ; Disaccharide reabsorption ; Maltase ; Brush border enzymes ; Microperfusion
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Renal tubular reabsorption of maltose, sucose and lactose were studied in vivo et situ by continuous microperfusion of single proximal convolutions of rat kidney. The14C-label of maltose (2.5 mmol/l) was removed from the lumen of the proximal tubule at about the same rate as found for glucose. Maltose reabsorption was completely inhibited in presence of 30 mmol/l glucose or of 0.1 mmol/l phlorizin. Chemical analysis of the samples showed a complete conversion of maltose into glucose within a perfusion distance of 2 mm. It is concluded from these results that within the tubular lumen maltose is split very rapidly by a brush border glucosidase. The short half time of this process permits the breakdown product glucose to be almost completely reabsorbed subsequently within the proximal tubule. In contrast, sucrose and lactose were neither split nor reabsorbed by the tubule brush border.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-2013
    Keywords: Amino acid transport ; Renal tubule ; Stereospecificity ; Passive diffusion ; Saturation kinetics
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Renal tubular reabsorption of glycine and of thel- andd-isomers of histidine, serine, phenylalamine, methionine, proline and cystine was investigated in vivo et situ by continuous microperfusion of single proximal convolutions of the rat kidney. In the case of glycine and thel-isomers, tubular reabsorption is saturable to a great extent. Thed-amino acids are reabsorbed much more slowly than the respectivel-forms. Furthermore in the case of methionine and perhaps also of proline, serine and phenylalanine, the fractional reabsorption decreases in the presence of high concentrations of thel-form. This indicates that thed-isomers also have a measurable affinity for the reabsorption mechanisms of the renal tubule. The very poor reabsorption ofd-amino acids in the presence of theirl-isomers indicates that simple passive diffusion plays only a relatively small role in tubular amino acid reabsorption. Permeability coefficients estimated from these findings are in the range from 1–5×10−7 cm2·s−1. These values are very similar to those found for other organic molecules of comparable molecular weights.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Metabolism of the Retinoid Ro 10-9359. Isolation and Identification of the Major Metabolites in Human Plasma, Urine and Feces Synthesis of Three Urinary MetabolitesAfter oral administration of therapeutic doses of the 3H-labelled aromatic retinoic acid analog (retinoid) Ro 10-9359 (ethyl all-trans-9-(4-methoxy-2,3,6-trimethyl-phenyl)-3,7-dimethyl-2,4,6,8-nonatetraenoate) to humans 75 and 15% of the 3H-dose were excreted within the first five days in the feces and the urine, respectively. Using chromatographic procedures including high pressure liquid chromatography 18 metabolites could be isolated from human urine. Their structures were elucidated by mass spectrometry and FT-1H-NMR. spectroscopy. In these urinary metabolites the tetraene side chain of the parent compound Ro 10-9359 is shortened. The radioactivity of the identified urinary metabolites accounted for about 11% of the dose. Three urinary metabolites were synthesized. The main part of the radioactivity excreted within the first five days in the feces consisted of unchanged drug (60% of the dose). A smaller (amount 15% of the dose) could not be identified. The unchanged drug and a major metabolite, the corresponding acid, were found in human plasma.In an experiment with bile-duct cannulated rats the radioactively labelled retinoid Ro 10-9359 was injected intravenously. About 70% of the 3H-dose was excreted in the bile, within the first 48 hours. The whole radioactivity of the rat bile consisted of polar metabolites. No unchanged drug could be found. After enzymatic hydrolysis of the bile conjugates three metabolites were isolated. The main metabolite (49% of the i.v. dose) was a conjugate of the corresponding acid of the parent drug, already found as free compound in human plasma. The other bile metabolites (9 and 7% of the i.v. dose) had an intact side chain, too.An enterohepatic recycling of the bile metabolites was observed in the rat.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several long chain primary alcohols (saturated, monoolefinic and methyl branched) have been converted via their mesylates into various long chain alkylated aromatic compounds with basic character, and their mass spectra compared. The spectra of 2-alkylaminopyridines and to some extent those of 3-alkylaminopyridines exhibit most clearly the structure of the aliphatic chain, allowing the localization of branchings and double bonds.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: One unsaturated and three branched long-chain primary alcohols have been converted into N-alkyl-2-pyrrolidones for investigation by mass spectrometry. The EI. mass spectra of these derivatives have been found to exhibit unambiguously the branching points and, albeit less clearly, the position of a double bond in the chain.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 111 (1978), S. 791-796 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Enehydrazines, 20: Pyrazolinium Betaines from 1,1-Dimethylhydrazine and 3-Phenylglycidic EstersEthyl trans-3-phenylglycidate and 1,1-dimethylhydrazine give the trans-4-hydroxy-5-phenyl-pyrazolinium betaine 1a, whereas the cis-phenylglycidic ester forms the cyclic cis-betaine 1b. Some degradation reactions are described.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 48 (1935), S. 92-95 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The base catalyzed rearrangement of 9,10,10-tricyano-5,9-methano-2,3,5,9-tetrahydro-cyclohepta[b]pyridines depends on the nature of the substituent at C(14). Seven products were isolated and identified. One structure resulting from a further ring closure was determined by x-ray analysis.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 112 (1979), S. 3237-3240 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Enehydrazines, 26. Heterocyclization of 1-(1,2-Dimethylhydrazino)-1-cyclohexen-3-oneThe reaction of the title compound 1 with methyl propiolate leads to the products 3a, 4a, and 5a, with dimethyl acetylenedicarboxylate to 3b, 4b, and 5b. Spectra and structures of the products are discussed.
    Notes: Umsetzung der Titelverbindung 1 mit Propiolsäure-methylester führt zu den Produkten 3a, 4a und 5a, mit Acetylendicarbonsäure-dimethylester zu 3b, 4b und 5b. Spektren und Konstitution der Produkte werden diskutiert.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 12 (1977), S. 351-369 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The mass spectra of the catenanes functionalized in one ring by β-phenylethylaza-, aza-, acetylaza-, trideuteroacetylaza- and trifluoroacetylaza groups respectively, are compared with the spectra of correspondingly substituted macrocyclic and long chain compounds. The mass spectra of most of the catenanes investigated are distinguished by a dominant fragmentation process, which isinitiated by the interannular transfer of ahydrogen atom to the functional group. Fragmentations caused by initial rupture of one of the macrocycles are much less favoured. Apart from H-transfer, no interannular reactions could be detected. In the presence of a β-phenylethylaza substituent, the loss of the benzyl radical is so fast, however, that no fragmentation initiated by H-transfer can be detected. The comparison of the spectra of the open chain compounds with the macrocyclic and catenane compounds suggests that significant solvation of these functional groups by long aliphatic chains does not exist.
    Notes: Die Massenspektren der Catenane, die in einem der beiden Ringe durch β-Phenyläthylaza-, Aza-, Acetylaza-, Trideuterioacetylaza- oder Trifluoracetylaza-Gruppen funktionalisiert sind, werden mit den Spektren entsprechend funktionalisierter makrocyclischer und langkettiger Moleküle verglichen. Die Massenspektren der meisten untersuchten Catenane zeichnen sich durch eine dominierende Fragmentierung aus, die durch eine interannulare H-Übertragung auf die funktionelle Gruppe eingeleitet wird. Fragmentierungen, die durch Ringbrüche eingeleitet werden, treten dagegen zurück. Abgesehen von H-Übertragungen sind keine interannularen Reaktionen nachweisbar. Bei Anwesenheif, einer β-Phenyläthylaza-Gruppe erfolgt der Verlust der Benzylgruppe so rasch, daβ keine bedeutende H-Übertragungsreaktion zustande kommt. Der Vergleich der Massenspektren der offenkettigen Verbindungen einerseits mit den makrocyclischen und catenan-artigen andererseits legt die Annahme nahe, daß eine bedeutende Solvatisierung der untersuchten funktionellen Gruppen durch lange Ketten nicht vorliegt.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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