Relevant bibliographies by topics / '.3-Dihydroxyflavone

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  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic ''.3-Dihydroxyflavone'

Author: Grafiati
Published: 22 June 2024
Last updated: 31 July 2025

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Journal articles on the topic "'.3-Dihydroxyflavone"

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Engelmann, Mark D., Ryan Hutcheson, and 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, no. 8 (2005): 2953–60. http://dx.doi.org/10.1021/jf048298q.

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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, no. 6 (2023): 794–63. http://dx.doi.org/10.6026/97320630019754.

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Paclitaxel is a widely used cancer chemotherapeutic agent for many solid tumors; but peripheral neuropathy is a major limitation for its clinical use. Studies have demonstrated the usefulness of flavone derivatives in chemotherapy induced peripheral neuropathy. The present study evaluates the anti-neuropathic effect of 3′, 4′-dihydroxyflavone on paclitaxel-induced peripheral neuropathy and the underlying mechanisms. Paclitaxel was administered to mice in a single dose of 10 mg/kg, i.p.The neuropathic behavioural parameters such as mechanical allodynia, cold allodynia and thermal hyperalgesia w
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Labarrière, Luc, Aurélien Moncomble, and Jean-Paul Cornard. "pH dependency of the structural and photophysical properties of the atypical 2′,3-dihydroxyflavone." RSC Advances 10, no. 58 (2020): 35017–30. http://dx.doi.org/10.1039/d0ra06833k.

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Nassira GHEMBAZA, Nabila BELYAGOUBI-BENHAMMOU, Amel ZITOUNI, Fethi TOUL, Serge MICHALET, and 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, no. 01 (2021): 15–23. http://dx.doi.org/10.46325/jnpra.v1i01.2.

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In the present paper, we are interested, for the first time, to separate and identify two glycosyl the flavones from Sedum villosum L, family Crassulaceae collected in the flowering phase in Lakhdar Oued, village of Tlemcen (Algeria). The crude methanolic extract of the flowers part was fractionated on column chromatography, and eluted with dichloromethane/methanol each time with increasing polarity of methanol; 24 fractions were separated. One of these fractions named F16 showed more antioxidant activity to scavenge DPPH free radical with percentage inhibition of 94.849 %. F16 was separated b
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Tasdemir, Deniz, Marcel Kaiser, Reto Brun, et al. "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, no. 4 (2006): 1352–64. http://dx.doi.org/10.1128/aac.50.4.1352-1364.2006.

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ABSTRACT Trypanosomiasis and leishmaniasis are important parasitic diseases affecting millions of people in Africa, Asia, and South America. In a previous study, we identified several flavonoid glycosides as antiprotozoal principles from a Turkish plant. Here we surveyed a large set of flavonoid aglycones and glycosides, as well as a panel of other related compounds of phenolic and phenylpropanoid nature, for their in vitro activities against Trypanosoma brucei rhodesiense, Trypanosoma cruzi, and Leishmania donovani. The cytotoxicities of more than 100 compounds for mammalian L6 cells were als
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Datta, Bidyut Kanti, Tahamina Iasmin, and Mohammad A. Rashid. "Further Flavonoids from Polygonum viscosum Buch-Ham. ex D. Don. (Polygonoceae)." Dhaka University Journal of Pharmaceutical Sciences 15, no. 1 (2016): 27–30. http://dx.doi.org/10.3329/dujps.v15i1.29189.

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Three additional flavonoids such as 5,7,4?-trihydroxy-3,8,3?-trimethoxy flavonol (1), 5,7-dihydroxyflavone (chrysin, 2) and 5,6,7-trihydroxyflavone (baicalein, 3) were obtained from the methanol extract of whole plant of Polygonum viscosum. The structure of the isolated compounds was established exclusively by ultraviolet (UV) spectroscopy, mass spectrometry (MS) and a series of Nuclear Magnetic Resonance (NMR) analysis.Dhaka Univ. J. Pharm. Sci. 15(1): 27-30, 2016 (June)
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Fatoki, Toluwase, Stanley Chukwuejim, Omodele Ibraheem, et al. "Harmine and 7,8-dihydroxyflavone synergistically suitable for amyotrophic lateral sclerosis management: An in silico study." Research Results in Pharmacology 8, no. 3 (2022): 49–61. http://dx.doi.org/10.3897/rrpharmacology.8.83332.

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Introduction: Amyotrophic lateral sclerosis (ALS) is a fatal neurological disease characterized by progressive degeneration of both upper and lower motor neurons, resulting in paralysis and eventually leads to death from respiratory failure typically within 3 to 5 years of symptom onset. The aim of this work was to predict the pharmacokinetics and identify unique protein targets that are associated with potential anti-ALS phytochemicals and FDA-approved drugs, by in silico approaches. Materials and methods: Standard computational tools (webserver and software) were used, and the methods used a
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Fatoki, Toluwase, Stanley Chukwuejim, Omodele Ibraheem, et al. "Harmine and 7,8-dihydroxyflavone synergistically suitable for amyotrophic lateral sclerosis management: An in silico study." Research Results in Pharmacology 8, no. (3) (2022): 49–61. https://doi.org/10.3897/rrpharmacology.8.83332.

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Introduction: Amyotrophic lateral sclerosis (ALS) is a fatal neurological disease characterized by progressive degeneration of both upper and lower motor neurons, resulting in paralysis and eventually leads to death from respiratory failure typically within 3 to 5 years of symptom onset. The aim of this work was to predict the pharmacokinetics and identify unique protein targets that are associated with potential anti-ALS phytochemicals and FDA-approved drugs, by in silico approaches. Materials and methods: Standard computational tools (webserver and software) were used, and the methods used a
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Espíndola, Cecilia. "Some Nanocarrier’s Properties and Chemical Interaction Mechanisms with Flavones." Molecules 28, no. 6 (2023): 2864. http://dx.doi.org/10.3390/molecules28062864.

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Flavones such as 7,8-dihydroxyflavone (tropoflavin), 5,6,7-trihydroxyflavone (baicalein), 3′,4′,5,6-tetrahydroxyflavone (luteolin), 3,3′,4′,5,5′,7-hexahydroxyflavone (myricetin), 4′,5,7-trihydroxyflavone (apigenin), and 5,7-dihydroxyflavone (chrysin) are important both for their presence in natural products and for their pharmacological applications. However, due to their chemical characteristics and their metabolic processes, they have low solubility and low bioavailability. Knowledge about the physicochemical properties of nanocarriers and the possible mechanisms of covalent and non-covalent
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Kim, Namkwon, Hyung-Seok Yoo, Yeon-Joo Ju, et al. "Synthetic 3',4'-Dihydroxyflavone Exerts Anti-Neuroinflammatory Effects in BV2 Microglia and a Mouse Model." Biomolecules & Therapeutics 26, no. 2 (2018): 210–17. http://dx.doi.org/10.4062/biomolther.2018.008.

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Dissertations / Theses on the topic "'.3-Dihydroxyflavone"

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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.

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Ce manuscrit présente les résultats d'une étude expérimentale et théorique de deux systèmes moléculaires d'intérêt environnemental : la 2',3-dihydroxyflavone (2'3HF) et les hydrocarbures aromatiques polycycliques (HAP). Ces systèmes ont été étudiés par une combinaison de techniques de spectroscopies électroniques (absorption et fluorescence) et de calculs de chimie quantique (DFT et TD-DFT). Dans une première partie de cette thèse, il est montré que la 2'3HF présente des propriétés acido-basiques singulières par rapport aux autres flavonols. La diminution de plusieurs unités de la valeur du pK
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Book chapters on the topic "'.3-Dihydroxyflavone"

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Teng, Hui, Hesham El-Seedi, and Lei Chen. "7,8-Dihydroxyflavone: Sources, Pharmacokinetics, Bioavailability, and Biological Effects." In Handbook of Dietary Flavonoids. Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-030-94753-8_85-1.

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You might also be interested in the extended bibliographies on the topic ''.3-Dihydroxyflavone' for particular source types:
Journal articles
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