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Titlebook: Bioactive Heterocycles VI; Flavonoids and Antho Noboru Motohashi Book 2008 Springer-Verlag Berlin Heidelberg 2008 DNA.antioxidant.biochemis

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發(fā)表于 2025-3-21 18:34:32 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
期刊全稱Bioactive Heterocycles VI
期刊簡稱Flavonoids and Antho
影響因子2023Noboru Motohashi
視頻videohttp://file.papertrans.cn/187/186460/186460.mp4
發(fā)行地址Heterocyclic chemistry is the biggest branch of chemistry covering two-third of the chemical literature.Covers hot topics of frontier research summarized by reputed scientists in the field.Our review
學(xué)科分類Topics in Heterocyclic Chemistry
圖書封面Titlebook: Bioactive Heterocycles VI; Flavonoids and Antho Noboru Motohashi Book 2008 Springer-Verlag Berlin Heidelberg 2008 DNA.antioxidant.biochemis
Pindex Book 2008
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沙發(fā)
發(fā)表于 2025-3-21 21:52:37 | 只看該作者
Multidrug Resistance Reversal on Cancer Cells by Selected Carotenoids, Flavonoids and Anthocyanins,flux activity was measured by the increase of rhodamine 123 (R123) uptake by cancer cells. The effects of flavonoids, carotenoids and anthocyanins were studied on the activity of the MDR-1 gene-encoded efflux pump system. The effective flavonoids were rotenone, chrysin, phloretin and sakuranetin, wh
板凳
發(fā)表于 2025-3-22 00:36:15 | 只看該作者
地板
發(fā)表于 2025-3-22 07:26:56 | 只看該作者
Jealousy, Femininity and Desireflux activity was measured by the increase of rhodamine 123 (R123) uptake by cancer cells. The effects of flavonoids, carotenoids and anthocyanins were studied on the activity of the MDR-1 gene-encoded efflux pump system. The effective flavonoids were rotenone, chrysin, phloretin and sakuranetin, wh
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發(fā)表于 2025-3-22 23:29:29 | 只看該作者
Realism Contested: Jean Améry’s the preparation of the most active Pgp inhibitor DHPs. This article specifically covers the MDR reversal activity. However, this article does not cover their cardiovascular or rest of the pharmacological activities shown of DHPs.
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發(fā)表于 2025-3-23 02:43:30 | 只看該作者
Antibacterial Activity of Artificial Phenothiazines and Isoflavones from Plants,es. Chlorpromazine and thioridazine were able to eliminate R-plasmids in drug-resistant bacteria. Artificially synthesized Benzo[.]phenothiazines could effectively suppress adenovirus oncogene expression. Phenothiazines have now been shown to inhibit efflux pumps in multidrug-resistant bacteria.
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發(fā)表于 2025-3-23 09:15:29 | 只看該作者
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