Auswahl der wissenschaftlichen Literatur zum Thema „'.3-Dihydroxyflavone“
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Zeitschriftenartikel zum Thema "'.3-Dihydroxyflavone":
Engelmann, Mark D., Ryan Hutcheson und I. Francis Cheng. „Stability of Ferric Complexes with 3-Hydroxyflavone (Flavonol), 5,7-Dihydroxyflavone (Chrysin), and 3‘,4‘-Dihydroxyflavone“. Journal of Agricultural and Food Chemistry 53, Nr. 8 (April 2005): 2953–60. http://dx.doi.org/10.1021/jf048298q.
Ramasamy, Kavitha. „3′, 4′-dihydroxyflavone ameliorates paclitaxel model of peripheral neuropathy in mice by modulating KATP channel, adenosine (A3) and GABAA (a2 subunit) receptors“. Bioinformation 19, Nr. 6 (30.06.2023): 794–63. http://dx.doi.org/10.6026/97320630019754.
Labarrière, Luc, Aurélien Moncomble und Jean-Paul Cornard. „pH dependency of the structural and photophysical properties of the atypical 2′,3-dihydroxyflavone“. RSC Advances 10, Nr. 58 (2020): 35017–30. http://dx.doi.org/10.1039/d0ra06833k.
Nassira GHEMBAZA, Nabila BELYAGOUBI-BENHAMMOU, Amel ZITOUNI, Fethi TOUL, Serge MICHALET und Fawzia ATIK- BEKKARA. „Rapid identification analysis of chemical constituents of Sedum villosum L. (Orpin.) by UHPLC-DAD-HRSM“. Journal of Natural Product Research and Applications 1, Nr. 01 (17.09.2021): 15–23. http://dx.doi.org/10.46325/jnpra.v1i01.2.
Tasdemir, Deniz, Marcel Kaiser, Reto Brun, Vanessa Yardley, Thomas J. Schmidt, Fatma Tosun und Peter Rüedi. „Antitrypanosomal and Antileishmanial Activities of Flavonoids and Their Analogues: In Vitro, In Vivo, Structure-Activity Relationship, and Quantitative Structure-Activity Relationship Studies“. Antimicrobial Agents and Chemotherapy 50, Nr. 4 (April 2006): 1352–64. http://dx.doi.org/10.1128/aac.50.4.1352-1364.2006.
Datta, Bidyut Kanti, Tahamina Iasmin und Mohammad A. Rashid. „Further Flavonoids from Polygonum viscosum Buch-Ham. ex D. Don. (Polygonoceae)“. Dhaka University Journal of Pharmaceutical Sciences 15, Nr. 1 (08.08.2016): 27–30. http://dx.doi.org/10.3329/dujps.v15i1.29189.
Fatoki, Toluwase, Stanley Chukwuejim, Omodele Ibraheem, Christiana Oke, Blessing Ejimadu, Isaiah Olaoye, Oluwabukola Oyegbenro et al. „Harmine and 7,8-dihydroxyflavone synergistically suitable for amyotrophic lateral sclerosis management: An in silico study“. Research Results in Pharmacology 8, Nr. 3 (25.08.2022): 49–61. http://dx.doi.org/10.3897/rrpharmacology.8.83332.
Espíndola, Cecilia. „Some Nanocarrier’s Properties and Chemical Interaction Mechanisms with Flavones“. Molecules 28, Nr. 6 (22.03.2023): 2864. http://dx.doi.org/10.3390/molecules28062864.
Kim, Namkwon, Hyung-Seok Yoo, Yeon-Joo Ju, Myung Sook Oh, Kyung-Tae Lee, Kyung-Soo Inn, Nam-Jung Kim und Jong Kil Lee. „Synthetic 3',4'-Dihydroxyflavone Exerts Anti-Neuroinflammatory Effects in BV2 Microglia and a Mouse Model“. Biomolecules & Therapeutics 26, Nr. 2 (01.03.2018): 210–17. http://dx.doi.org/10.4062/biomolther.2018.008.
Šimunková, Miriama, und Michal Malček. „Dimethyl sulfoxide as a strongly coordinating solvent: 3′,4′-dihydroxyflavone-Cu(II)-DMSO system case study“. Acta Chimica Slovaca 13, Nr. 2 (01.10.2020): 38–48. http://dx.doi.org/10.2478/acs-2020-0022.
Dissertationen zum Thema "'.3-Dihydroxyflavone":
Labarrière, Luc. „Spectroscopic properties of environmental relevant systems : 2’,3-dihydroxyflavone-ion complexes and polycyclic aromatic hydrocarbons : a joint experimental and theoretical study“. Electronic Thesis or Diss., Université de Lille (2022-....), 2022. http://www.theses.fr/2022ULILR069.
This manuscript reports the results of an experimental and theoretical study of two molecular systems of environmental interest: 2',3-dihydroxyflavone (2'3HF) and polycyclic aromatic hydrocarbons (PAH). These systems were studied by a combination of electronic spectroscopic techniques (absorption and fluorescence) and quantum chemical calculations (DFT and TD-DFT). In the first part of this thesis, it is shown that 2'3HF has singular acid-base properties compared to other flavonols. The decrease of the pKa by several units is attributed to the presence of a hydrogen-bond network. In the excited state, an intramolecular proton transfer causes a dual fluorescence. An additional emission band, seemingly originating from a tautomeric form perturbed by interaction with the solvent, was revealed. Finally, an exhaustive study of the Ca(II), Mn(II) and Zn(II) complexes showed the formation of chelates with the α-hydroxyketone function. In the second part, three structural hypotheses to explain the experimental observation of visible-range laser-induced fluorescence (LIF) were explored. A study of van der Waals (vdW) dimers of PAHs provided insights into the nature of the monomer interaction and highlighted the difficulty of modelling these systems. However, the calculated electronic transitions suggest that these species cannot be responsible for the LIF signals. Secondly, an identical study of aliphatically bridged PAHs showed very similar results to vdW dimers, ruling out their involvement in the observed fluorescence. Finally, the hypothesis of emission from PAH radicals was explored. The latter is very promising and opens the way for further experimental and theoretical studies
Buchteile zum Thema "'.3-Dihydroxyflavone":
Teng, Hui, Hesham El-Seedi und Lei Chen. „7,8-Dihydroxyflavone: Sources, Pharmacokinetics, Bioavailability, and Biological Effects“. In Handbook of Dietary Flavonoids, 1–12. Cham: Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-030-94753-8_85-1.