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'Coumarin' in keywords
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1Author    VirinderS. Parmar, HirdayN. Jha, SudershanK. Sanduja, Radhika SandujaRequires cookie*
 Title    Trigocoumarin -a New Coumarin from Trigonella foenumgraecum  
 Abstract    A new coumarin, named trigocoumarin has been isolated from Trigonella foenumgraecum along with some known compounds. Based upon its spectral (IR, UV, NMR and MS) and analytical data, trigocoumarin has been assigned the structure: 3-(ethoxycarbonyl)-methy 1 -4 -methyl -5,8-dimethoxy coumarin. 
  Reference    Z. Naturforsch. 37b, 521—523 (1982); received October 8 1981 
  Published    1982 
  Keywords    Trigonella foenumgraecum, Leguminoseae, Coumarin 
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 TEI-XML for    default:Reihe_B/37/ZNB-1982-37b-0521.pdf 
 Identifier    ZNB-1982-37b-0521 
 Volume    37 
2Author    StewartA. BrownRequires cookie*
 Title    Biosynthesis of Daphnetin in Daphne mezereum L.  
 Abstract    Shoots of Daphne mezereum synthesized daphnetin (7,8-dihydroxycoumarin) more efficiently from [2-l4C]umbelliferone (7-hydroxycoumarin) than from [2-l4C]p-coumaric acid, and [2-14C]caf-feic acid was more poorly utilized still. These findings do not support the idea of derivation of daphnetin via hydroxylation of the caffeic acid ring at the 2 position, followed by lactone ring formation; instead they are consistent with the concept of daphnetin formation by an additional hydroxylation of umbelliferone at C-8. Umbelliferone was recovered with little l4C dilution from emulsin-hydrolysed extracts of shoots fed labelled umbelliferone, and TLC of extracts from un­ treated shoots revealed two substances yielding umbelliferone on hydrolysis. Evidence is pre­ sented from TLC and HPLC analysis that one of these is skimmin (7-O-ß-D-glucosylumbel-liferone), not previously reported from Daphne. The tracer experiments further support the theory that umbelliferone is the general precursor of coumarins bearing two or more hydroxyl functions on the aromatic ring. 
  Reference    Z. Naturforsch. 41c, 247 (1986); received November 4 1985 
  Published    1986 
  Keywords    Biosynthesis, Coumarins, Daphne mezereum, Daphnetin 
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 TEI-XML for    default:Reihe_C/41/ZNC-1986-41c-0247.pdf 
 Identifier    ZNC-1986-41c-0247 
 Volume    41 
3Author    M. Aya, IvM. Itova3, MinchoE. Anchevb, StefanG. Panev3, N. Edjalka, V. H. Andjieva3, Sim Eon, S. Popov3Requires cookie*
 Title    Coumarins and Iridoids from Crucianella graeca, Cruciata glabra, Cruciata laevipes and Cruciata pedemontana (Rubiaceae)  
 Abstract    The coumarin and iridoid composition of Crucianella graeca, Cruciata glabra, Cruciata laevipes and Cruciata pedemontana has been studied. Daphnin and daphnetin glucoside do­ minated in C. glabra along with low concentrations of daphnetin, deacetylasperulosidic acid and scandoside. In C. laevipes and C. pedemontana were found the same coumarin glucosides along with six iridoid glucosides. In Crucianella graeca were found ten iridoid glucosides. 
  Reference    Z. Naturforsch. 51c, 631 (1996); received May 23/July 8 1996 
  Published    1996 
  Keywords    Rubiaceae, Crucianella, Cruciata, Coumarins, Iridoids 
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 TEI-XML for    default:Reihe_C/51/ZNC-1996-51c-0631.pdf 
 Identifier    ZNC-1996-51c-0631 
 Volume    51 
4Author    KarinM. Valant-Vetscheraa, Eckhard WollenweberbRequires cookie*
 Title    Flavonoid Aglycones from the Leaf Surfaces of Some Artemisia spp. (Com positae-Anthem ideae)  
 Abstract    Several species of the large genus Artemisia have been analysed for the flavonoid aglycone composition of their leaf exudates. These species belong to different taxonomic groups within Artemisia. Flavone and flavonol aglycones were found as the major flavonoid constituents of the leaf exudates. Many of these compounds were 6-methoxylated, with additional substitu­ tions at the 7-, 3'-and 4'-position of the molecule. In addition, 7,4'-substituted apigenin and luteolin derivatives and rarely also coumarin derivatives were encountered in some species. The observed substitution trends are in accordance with literature data. Taxonomic and eco­ logical aspects are briefly discussed. 
  Reference    Z. Naturforsch. 50c, 353—357 (1995); received January 23/February 27 1995 
  Published    1995 
  Keywords    Artemisia, Compositae-Anthemideae, Leaf Exudates, Flavones, Coumarins 
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 TEI-XML for    default:Reihe_C/50/ZNC-1995-50c-0353.pdf 
 Identifier    ZNC-1995-50c-0353 
 Volume    50 
5Author    HerbertOliver Kolodziej3, HermanJ. Kayser3, Wim Woerdenbagb, Niesko Van Udenb, PrasRequires cookie*
 Title    Structure -Cytotoxicity Relationships of a Series of Natural and Semi-Synthetic Simple Coumarins as Assessed in Two Human Tumour Cell Lines  
 Abstract    The cytotoxicity of 22 natural and semi-synthetic simple coumarins was evaluated in G LC4, a human small cell lung carcinoma cell line, and in CO LO 320. a human colorectal cancer cell line, using the microculture tetrazolium (MTT) assay. With IC 50 values > 100 j.i m , following a continuous (96h) incubation, most coumarins exhibited only low cytotoxicity. Several com­ pounds, however, displayed significant potencies. As far as the structure -cytotoxicity rela­ tionship is concerned, it is conspicuous that all the potentially active natural compounds possess at least two phenolic groups in either the 6,7-or 6,8-positions. In addition, the 5-formyl-6-hydroxy substituted semi-synthetic analogue was found to be potent, reflecting the importance of at least two polar functions for high cytotoxicity. 
  Reference    Z. Naturforsch. 52c, 240—244 (1997); received November ll/December 5 1996 
  Published    1997 
  Keywords    Coumarins, Cytotoxicity, Structure-Activity Relationships, Pelargonium sidoides, Geraniaceae 
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 TEI-XML for    default:Reihe_C/52/ZNC-1997-52c-0240.pdf 
 Identifier    ZNC-1997-52c-0240 
 Volume    52 
6Author    Oliver Kayser, H. Erbert KolodziejRequires cookie*
 Title    Antibacterial Activity of Simple Coumarins: Structural Requirements for Biological Activity  
 Abstract    The antibacterial activity of a series of simple coumarins was evaluated against 8 microor­ ganisms, including three Gram-positive (Staphylococcus aureus, beta-hemolytic Streptococcus and Streptococcus pneum oniae) and five Gram-negative bacteria (Escherichia coli, Klebsiella pneum oniae, Pseudom onas aeruginosa, Proteus mirabilis and H aemophilus influenzae), using the microdilution broth method. The coumarins tested showed broad diversity regarding growth inhibitory activity with minimum inhibitory concentrations ranging from 0.9 to >12.4 (j.M . This study, presenting the first systematic analysis of structure-activity relationships among this group of coumarins, revealed some interesting structural requirements. While coumarins with a methoxy function at C-7 and, if present, an OH group at either the C-6 or C-8 position are invariably effective against the spectrum of tested standard bacteria (Gram-negative microorganisms including the Gram-positive bacterium Staphylococcus aureus), the presence of an aromatic dimethoxy arrangement is apparently favourable against those mi­ croorganisms which require special growth factors (beta-hemolytic Streptococcus, Streptococ­ cus pneum oniae and Haem ophilus influenzae). A combination of these structural features, two methoxy functions and at least one additional phenolic group as reflected by the highly oxygenated coumarins, identify promising candidates with antibacterial broad-spectrum ac­ tivity. 
  Reference    Z. Naturforsch. 54c, 169—174 (1999); received November 11/December 8 1998 
  Published    1999 
  Keywords    Coumarins, Antibacterial Activity, Structure-Activity Relationships 
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 TEI-XML for    default:Reihe_C/54/ZNC-1999-54c-0169.pdf 
 Identifier    ZNC-1999-54c-0169 
 Volume    54 
7Author    A. Bączyński, P. Targowski, B. Ziętek, D. RadomskaRequires cookie*
 Title    Fluorescence Spectra and Determination of the Energy of O-O Transitions of Coumarins in Liquid Solutions  
 Abstract    Analytical expressions of absorption and fluorescence spectra of some coumarins in ethyl alcohol at room temperature are given. Satisfactory agreement of measured and calculated spectra is obtained. It was possible to obtain the pure electronic transition energies immediately after excita-tion (from absorption spectra) and after the thermal and orientational equilibrium is reached (from fluorescence). An optical transition carries a dye-solvent system to a state in which the mutual interaction energy is larger than in the initial state. 
  Reference    Z. Naturforsch. 45a, 618—622 (1990); received September 29 1989 
  Published    1990 
  Keywords    Photoluminescence of solutions, Shapes of molecular spectra, Coumarins 
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 TEI-XML for    default:Reihe_A/45/ZNA-1990-45a-0618.pdf 
 Identifier    ZNA-1990-45a-0618 
 Volume    45 
8Author    A. Bączyński, P. Targowski, B. Ziętek, D. RadomskaRequires cookie*
 Title    Franck-Condon States of Coumarins in Alcoholic Solutions  
 Abstract    The temperature dependence of the fluorescence spectra of coumarin 2, coumarin 10 and cou-marin 120 in ethyl alcohol is investigated. A blue-shift of the spectra with increase of temperature is observed. The blue-shift is explained by means of excited and ground Franck-Condon state parameters obtained by the adjustment of analytical shape factors to experimental spectra. 
  Reference    Z. Naturforsch. 45a, 1349—1353 (1990); received March 6 1990 
  Published    1990 
  Keywords    Photoluminescence of solutions, Shapes of molecular spectra, Coumarins 
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 TEI-XML for    default:Reihe_A/45/ZNA-1990-45a-1349.pdf 
 Identifier    ZNA-1990-45a-1349 
 Volume    45 
9Author    Fiirstner, DenisN. Jumbam, Nongyuan ShiRequires cookie*
 Title    Alois  
 Abstract    Low-valent titanium prepared by the reduction of TiCl3 with zinc dust oxidatively adds to a-ketoam ides or a-ketoesters with the formation of the corresponding titanium enediolates. These 1,2-difunctional nucleophiles, which have hardly been used in organic synthesis so far, undergo regioselective intramolecular aldol condensation reactions with various electrophiles such as aldehydes, ketones, nitriles, esters and amides. This methodology allows the synthesis of differently substituted coumarin and 2-quinolone derivatives. 
  Reference    Z. Naturforsch. 50b, 326—332 (1995); received September 13 1994 
  Published    1995 
  Keywords    Low-Valent Titanium, Enediolates, Coumarins, 2-Quinolones, Aldol Condensation 
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 TEI-XML for    default:Reihe_B/50/ZNB-1995-50b-0326.pdf 
 Identifier    ZNB-1995-50b-0326 
 Volume    50 
10Author    SatishK. Sharma, JinnieM. Garrett, StewartA. BrownRequires cookie*
 Title    Separation of the S-Adenosylmethionine: 5-and 8-Hydroxyfuranocoumarin O-Methyltransferases of Ruta graveolens L. by General Ligand Affinity Chromatography  
 Abstract    Two S-adenosyl-L-methionine:furanocoumarin O-methyltransferases of R . graveolens, acting at the 5-and 8-hydroxyls of the psoralen nucleus, were completely resolved by adsorption on a general affinity ligand, 5 -(3-carboxypropanamido) xanthotoxin, followed by specific desorption by bergaptol and xanthotoxol, respectively. The 5-O-methyltransferase was purified 450-fold by this procedure, the 8-O-methyltransferase 112-fold, and both enzyme fractions were electrophoretically homogeneous. No resolution could be achieved of the activity against two 5-hydroxypsoralens or of the activity against two 8-hydroxypsoralens, and conclusive evidence is presented for the existence of only one 5-O-methyltransferase and only one 8-O-methyltransferase acting on linear furanocoumarins. In tro d u c tio n 
  Reference    Z. Naturforsch. 34c, 387 (1979); received March 9 1979 
  Published    1979 
  Keywords    Coumarins, Furanocoumarins, O-Methyltransferases, Affinity Chromatography, R u ta graveolens 
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 TEI-XML for    default:Reihe_C/34/ZNC-1979-34c-0387.pdf 
 Identifier    ZNC-1979-34c-0387 
 Volume    34