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  • Bentham Science Publishers Ltd.  (2)
  • Wang, Xiuxiu  (2)
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  • Bentham Science Publishers Ltd.  (2)
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  • 1
    Online Resource
    Online Resource
    Bentham Science Publishers Ltd. ; 2022
    In:  Letters in Organic Chemistry Vol. 19, No. 1 ( 2022-01), p. 59-63
    In: Letters in Organic Chemistry, Bentham Science Publishers Ltd., Vol. 19, No. 1 ( 2022-01), p. 59-63
    Abstract: A novel, mild and efficient protocol to synthesize dibrominated propanamides has been developed. The presented methodology provides several merits, such as easy-to-handle and stable brominated substrate, catalyst-free, additive free and facile experimental operation. The preliminary mechanism study indicated that a free radical pathway might be involved in the presented reaction.
    Type of Medium: Online Resource
    ISSN: 1570-1786
    Language: English
    Publisher: Bentham Science Publishers Ltd.
    Publication Date: 2022
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  • 2
    In: Anti-Cancer Agents in Medicinal Chemistry, Bentham Science Publishers Ltd., Vol. 23, No. 7 ( 2023-04), p. 779-785
    Abstract: Cancer is associated with metabolic changes from increased cell proliferation and growth. Compared to normal differentiated cells, MM cells use the glycolytic pathway even when adequate oxygen is present triggering “Glutamine addiction”. Objective: To investigate the single and combined effects of epigallocatechin-3-gallate (EGCG) and telaglenastat, a glutaminase inhibitor, on the proliferation and apoptosis of the multiple myeloma cell line KM3/BTZ. Methods: KM3/BTZ cells were treated with different concentrations of telaglenastat and EGCG alone or in combination to investigate their effect on proliferation and apoptosis using the CCK8 assay, flow cytometry, and western blotting. The Chou-Talalay combination index analysis was used to explore the effect of telaglenastat combined with EGCG, while the Combination Index (CI) was calculated to analyze whether the combination of the two drugs had a synergistic effect. Results: Telaglenastat and EGCG alone as well as in combination (5 μmol/L telaglenastat + 120 μmol/L EGCG) significantly inhibited the proliferation of KM3/BTZ cells compared to the inhibition effect of the control. Additionally, the combined treatment increased the proportion of KM3/BTZ cells in the G2 phase and decreased the proportion of cells in the G1 phase. The apoptosis rate of EGCG alone and the combined treatment was significantly higher than that of the control group. Bax protein expression was highest in the combined treatment group, whereas Bcl-2 expression was lowest, with the combined treatment group having the highest ratio of Bax/Bcl-2. Conclusion: Telaglenastat and EGCG act synergistically to inhibit cell proliferation and promote apoptosis in KM3/BTZ cells, possibly by targeting glutamine metabolism and glycolysis.
    Type of Medium: Online Resource
    ISSN: 1871-5206
    Language: English
    Publisher: Bentham Science Publishers Ltd.
    Publication Date: 2023
    SSG: 15,3
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