麻醉椒苫素
Methysticin
产品名称 |
产品编号 |
CAS编号 |
包装 |
QQ客服 |
麻醉椒苫素 |
CFN90160 |
20697-20-5 |
1mg |
QQ客服:2159513211 |
麻醉椒苫素 |
CFN90160 |
20697-20-5 |
5mg |
QQ客服:2159513211 |
麻醉椒苫素 |
CFN90160 |
20697-20-5 |
10mg |
QQ客服:2159513211 |
麻醉椒苫素 |
CFN90160 |
20697-20-5 |
20mg |
QQ客服:2159513211 |
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ChemFaces的产品在许多优秀和顶级科学期刊中被引用
Cell. 2018 Jan 11;172(1-2):249-261.e12. doi: 10.1016/j.cell.2017.12.019.
IF=36.216(2019)PMID: 29328914
Cell Metab. 2020 Mar 3;31(3):534-548.e5. doi: 10.1016/j.cmet.2020.01.002.
IF=22.415(2019)PMID: 32004475
Mol Cell. 2017 Nov 16;68(4):673-685.e6. doi: 10.1016/j.molcel.2017.10.022.
IF=14.548(2019)PMID: 29149595
ACS Nano. 2018 Apr 24;12(4): 3385-3396. doi: 10.1021/acsnano.7b08969.
IF=13.903(2019)PMID: 29553709
Nature Plants. 2016 Dec 22;3: 16206. doi: 10.1038/nplants.2016.205.
IF=13.297(2019)PMID: 28005066
Sci Adv. 2018 Oct 24;4(10): eaat6994. doi: 10.1126/sciadv.aat6994.
IF=12.804(2019)PMID: 30417089
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国外学术期刊发表的引用ChemFaces产品的部分文献
Description: |
Methysticin is a potent NF-kappaB inhibitor in kava with minimum toxicity, it possesses hepatotoxic, anticonvulsant and neuroprotective properties, it contributes to CYP1A1 induction. |
Targets: |
P450 (e.g. CYP17) | NF-kB | Calcium Channel | Potassium Channel |
In vitro: |
Phytother Res. 2011 Mar;25(3):417-23. | Kavalactones Yangonin and Methysticin induce apoptosis in human hepatocytes (HepG2) in vitro.[Pubmed: 20734326] | While cases of severe kava hepatotoxicity have been reported, studies examining the toxicity of individual kavalactones are limited. The present study examined the in vitro hepatotoxicity of kavain, Methysticin and yangonin on human hepatocytes (HepG2) and the possible mechanism(s) involved.
METHODS AND RESULTS:
Cytotoxicity was assessed using lactate dehydrogenase (LDH) and ethidium bromide (EB) assays. The mode of cell death was analysed with acridine orange/ethidium bromide dual staining with fluorescence microscopy. Glutathione oxidation was measured using the ortho-phthalaldehyde (OPT) fluorescence assay. Kavain had minimal cytotoxicity, Methysticin showed moderate concentration-dependent toxicity and yangonin displayed marked toxicity with ~ 40% reduction in viability in the EB assay. Acridine orange/ethidium bromide staining showed the predominant mode of cell death was apoptosis rather than necrosis. No significant changes were observed in glutathione levels, excluding this as the primary mechanism of cell death in this model. Further studies may elucidate the precise apoptotic pathways responsible and whether toxic kavalactone metabolites are involved. | Naunyn Schmiedebergs Arch Pharmacol. 1995 Apr;351(4):348-55. | Effects of methysticin on three different models of seizure like events studied in rat hippocampal and entorhinal cortex slices.[Pubmed: 7630425] | Methysticin is one of the constituents of Piper methysticum which possesses anticonvulsant and neuroprotective properties.
METHODS AND RESULTS:
Its effects on different in vitro seizure models were tested using extracellular recordings in rat temporal cortex slices containing the hippocampus and the entorhinal cortex. Elevating [K+]0 induced seizure-like events with tonic and clonic electrographic phases in area CA1. Lowering [Ca2+]0 caused recurrent seizure like episodes with large negative field potential shifts. Lowering Mg2+ induced short recurrent discharges in area CA3 and CA1 while ictaform events lasting for many seconds were induced in the subiculum, entorhinal and temporal neocortex. In the hippocampus the activity stayed stable over a number of hours. In contrast, the ictaform events in the subiculum, entorhinal and temporal cortex changed their characteristics after one to two hours to late recurrent discharges. In a concentration-range from 10 to 100 microM Methysticin reversibly blocked all these types of epileptiform activity. Decreases in [Ca2+]0 and associated slow field potentials evoked by repetitive stimulation of the stratum radiatum or the alveus remained almost unaffected by Methysticin. A paired pulse stimulus paradigm used to test for effects of Methysticin on synaptically evoked transient field potentials in normal medium revealed interference with mechanisms involved in frequency potentiation. While responses to alvear stimulation were largely unaffected, the responses to a paired pulse stimulus to stratum radiatum were depressed over the whole range of tested stimulus intervals. CONCLUSIONS: The findings suggest that Methysticin has effects on different patterns of epileptiform activity possibly by interfering with processes responsible for frequency potentiation. |
|
|
1 mg |
5 mg |
10 mg |
20 mg |
25 mg |
1 mM |
3.646 mL |
18.2302 mL |
36.4604 mL |
72.9208 mL |
91.1511 mL |
5 mM |
0.7292 mL |
3.646 mL |
7.2921 mL |
14.5842 mL |
18.2302 mL |
10 mM |
0.3646 mL |
1.823 mL |
3.646 mL |
7.2921 mL |
9.1151 mL |
50 mM |
0.0729 mL |
0.3646 mL |
0.7292 mL |
1.4584 mL |
1.823 mL |
100 mM |
0.0365 mL |
0.1823 mL |
0.3646 mL |
0.7292 mL |
0.9115 mL |
* Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
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