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Acacetin

About: Acacetin is a research topic. Over the lifetime, 442 publications have been published within this topic receiving 10458 citations. The topic is also known as: 5,7-Dihydroxy-2-(4-methoxyphenyl)-4-benzopyrone & Linarigenin.


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Journal ArticleDOI
TL;DR: Results indicated that chrysin and 4',7-dimethylnarangenin inhibited the acceptor side of PS II, and Flavonoids also showed activity on the growth of seedlings of Lolium perenne and Echinochloa crus-galli.
Abstract: As a continuous effort to find new natural products with potential herbicide activity, flavonoids acacetin (1), chrysin (2) and 4',7-dimethylnarangenin (3) were isolated from a propolis sample collected in the rural area of Mexico City and their effects on the photosynthesis light reactions and on the growth of Lolium perenne, Echinochloa crus-galli and Physalis ixocarpa seedlings were investigated. Acacetin (1) acted as an uncoupler by enhancing the electron transport under basal and phosphorylating conditions and the Mg(2+)-ATPase. Chrysin (2) at low concentrations behaved as an uncoupler and at concentrations up to 100 μM its behavior was as a Hill reaction inhibitor. Finally, 4',7-dimethylnarangenin (3) in a concentration-dependent manner behaved as a Hill reaction inhibitor. Flavonoids 2 and 3 inhibited the uncoupled photosystem II reaction measured from water to 2,5-dichloro-1,4-benzoquinone (DCBQ), and they did not inhibit the uncoupled partial reactions measured from water to sodium silicomolybdate (SiMo) and from diphenylcarbazide (DPC) to diclorophenol indophenol (DCPIP). These results indicated that chrysin and 4',7-dimethylnarangenin inhibited the acceptor side of PS II. The results were corroborated with fluorescence of chlorophyll a measurements. Flavonoids also showed activity on the growth of seedlings of Lolium perenne and Echinochloa crus-galli.

9 citations

Journal Article
TL;DR: The chemical constituents of the flowers of Chrysanthemum indicum are studied by isolated and purified by silica gel and Sephadex LH-20 column chromatography.
Abstract: Objective To study the chemical constituents of the flowers of Chrysanthemum indicum. Methods Chemical constituents were isolated and purified by silica gel and Sephadex LH-20 column chromatography. The structures were identified by means of physico-chemical and spectral data. Results From the 80% ethanol extract of the material, seven compounds were isolated. Their structures were identified as acacetin(1), acacetin-7-O-(6"-O-acetyl) beta-D-glucopyranoside (2), linarin (3), apigenin-7-O-beta-D-glucopyranoside(4), chlorogenic acid (5), vanillic acid(6) and sucrose(7), respectively. Conclusion Compounds 2, 4, 6 and 7 are isolated from C. indicum for the first time.

9 citations

Journal ArticleDOI
TL;DR: The investigated specimens of this species can be divided into two groups on the basis of the presence or absence in them of 6-methoxykaempferide, which was characterized by larger leaf-blades containing this compound, whereas it was absent in group II with smaller leaves.
Abstract: Betula pendula Roth. leaves were found to contain, beside the flavonoids detected earlier by other researchers, isorhamnetin 3-galactoside, acacetin 7-glucoside, and perhaps scutellarein 7-glycoside and quercetin 3-glycoside-7,4'-dimethyl ether. The investigated specimens of this species can be divided into two groups on the basis of the presence or absence in them of 6-methoxykaempferide. Group I was characterized by larger leaf-blades containing this compound, whereas it was absent in group II with smaller leaves. The composition of the leaf flavonoids of B. obscura Kot. samples was identical with that of the specimens of the above-mentioned small leaved B. pendula .

9 citations

Journal ArticleDOI
TL;DR: Data indicate that acacetin‐induced cell apoptosis in HNSCC cells may be through M3R related calcium signaling and caspase 3 activation, which is a potent natural antitumor reagent especially for the tumor cells, which highly expressed M 3R.
Abstract: Aacacetin, a plant flavone has shown antitumor efficacy recently. However, its associated mechanisms are poorly known. We hypothesized that the muscarinic M3 receptor (M3 R), which is highly expressed in some cancer tissue, is related to the antitumor effect of acacetin in head and neck squamous cell carcinoma (HNSCC) cells. Our results showed that 12.5- to 200-μM acacetin inhibited cell viability in dose- and time-dependent manners in HNSCC cells, but a relative higher concentration was needed for oral adenoid cystic carcinoma cells. M3 R expression level was higher in HNSCC cells than that in adenoid cystic carcinoma cells. Flow cytometry and electron microscopy confirmed acacetin-induced cell apoptosis in 22B cells, a HNSCC cell line. Acacetin promoted mitochondrial cytochrome c release and caspase 9, 3 processing. Knocking down of M3 R expression by specific siRNA significantly prevented the acacetin-induced cell viability damage, cell apoptosis, and caspase 3 activation. Besides, M3 R was also involved in acacetin-induced elevation of reactive oxygen species and intracellular calcium ([Ca2+ ]i ). These data indicate that acacetin-induced cell apoptosis in HNSCC cells may through M3 R related calcium signaling and caspase 3 activation. Acacetin is a potent natural antitumor reagent especially for the tumor cells, which highly expressed M3 R.

9 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
202320
202252
202127
202031
201923
201818