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  • 醉茄内酯 A

    Withanolide A

    醉茄内酯 A
    产品编号 CFN91964
    CAS编号 32911-62-9
    分子式 = 分子量 C28H38O6 = 470.60
    产品纯度 >=98%
    物理属性 Powder
    化合物类型 Steroids
    植物来源 The herbs of Physali alkekengi
    ChemFaces的产品在影响因子大于5的优秀和顶级科学期刊中被引用
    提供自定义包装
    产品名称 产品编号 CAS编号 包装 QQ客服
    醉茄内酯 A CFN91964 32911-62-9 1mg QQ客服:2159513211
    醉茄内酯 A CFN91964 32911-62-9 5mg QQ客服:2159513211
    醉茄内酯 A CFN91964 32911-62-9 10mg QQ客服:2159513211
    醉茄内酯 A CFN91964 32911-62-9 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
    我们的产品现已经出口到下面的研究机构与大学,并且还在增涨
  • Institute of Bioorganic Chemistry Polish Academy of Sciences (Poland)
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  • University of Cincinnati (USA)
  • Fraunhofer-Institut für Molekularbiologie und Angewandte ?kologie IME (Germany)
  • Utah State University (USA)
  • Universidad de Buenos Aires (Argentina)
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  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Current Topics in Nutraceutical Research2021, 19(1),p90-105.
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  • Biomed Pharmacother.2022, 146:112497.
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  • Exp Parasitol.2015, 153:160-4
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  • Molecules2022, 27(9):2613.
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  • Recent Pat Anticancer Drug Discov.2022, 17(4):416-426.
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  • ...
  • 生物活性
    Description: Withanolide A extends the lifespan in human EGFR-driven cancerous Caenorhabditis elegans. Withanolide A may serve as potential neuroprotective agent due to inhibition of MAPK family proteins and activation of PI3K/Akt signaling, it plays an important role in central muscarinic receptor functional balance and activation of antioxidant system in the cerebral cortex of temporal lobe epileptic condition. Withanolide A shows anticancer activity against the SK-Br-3 cells.
    Targets: EGFR | NF-kB | TNF-α | Caspase | ROS | NMDAR | PI3K | Akt | MAPK
    In vitro:
    Drug Des Devel Ther. 2017 Jun 22;11:1859-1870.
    Molecular docking, QSAR and ADMET studies of withanolide analogs against breast cancer.[Pubmed: 28694686 ]
    Withanolides are a group of pharmacologically active compounds present in most prodigal amounts in roots and leaves of Withania somnifera (Indian ginseng), one of the most important medicinal plants of Indian traditional practice of medicine. Withanolides are steroidal lactones (highly oxygenated C-28 phytochemicals) and have been reported to exhibit immunomodulatory, anticancer and other activities.
    METHODS AND RESULTS:
    In the present study, a quantitative structure activity relationship (QSAR) model was developed by a forward stepwise multiple linear regression method to predict the activity of Withanolide Analogs against human breast cancer. The most effective QSAR model for anticancer activity against the SK-Br-3 cell showed the best correlation with activity (r2=0.93 and rCV2 =0.90). Similarly, cross-validation regression coefficient (rCV2=0.85) of the best QSAR model against the MCF7/BUS cells showed a high correlation (r2=0.91). In particular, compounds CID_73621, CID_435144, CID_301751 and CID_3372729 have a marked antiproliferative activity against the MCF7/BUS cells, while 2,3-dihydrowithaferin A-3-beta-O-sulfate, withanolide 5, Withanolide A, withaferin A, CID_10413139, CID_11294368, CID_53477765, CID_135887, CID_301751 and CID_3372729 have a high activity against the Sk-Br-3 cells compared to standard drugs 5-fluorouracil (5-FU) and camptothecin.
    CONCLUSIONS:
    Molecular docking was performed to study the binding conformations and different bonding behaviors, in order to reveal the plausible mechanism of action behind higher accumulation of active Withanolide Analogs with β-tubulin. The results of the present study may help in the designing of lead compound with improved activity.
    Mol Neurobiol. 2018 Apr;55(4):2725-2739.
    Attenuation of Glutamate-Induced Excitotoxicity by Withanolide-A in Neuron-Like Cells: Role for PI3K/Akt/MAPK Signaling Pathway.[Pubmed: 28447311 ]
    Glutamate-induced excitotoxicity is one of the major underlying mechanisms for neurodegenerative diseases. Efforts are being made to treat such conditions with an array of natural compounds that can modulate the release of glutamate or the underlying mechanisms associated with it. Withania somnifera extract has potent pharmacologic activity similar to that of Korean Ginseng tea and is used to treat several neuronal disorders. However, to date, little efforts have been made to evaluate individual constituents of this plant for neurodegenerative disorders.
    METHODS AND RESULTS:
    Present study was carried out to investigate withanolide A, one of the active constituents of Withania somnifera against glutamate-induced excitotoxicity in retinoic acid differentiated Neuro2a neuroblastoma cells. The results indicated that glutamate treatment for 2 h induced death in cells that was significantly attenuated by pre-treatment with MK-801 (specific NMDA receptor antagonist) and different concentrations of withanolide A. Withanolide A abated the glutamate-induced influx of intracellular calcium and excessive ROS production significantly. Further on, glutamate treatment resulted in increased levels of pro-apoptotic and decreased levels of anti-apoptotic proteins, and these protein levels were normalized by various doses of withanolide A.
    CONCLUSIONS:
    All of these protective effects were partly due to inhibition of MAPK family proteins and activation of PI3K/Akt signaling. Thus, our results suggest that withanolide A may serve as potential neuroprotective agent.
    In vivo:
    Biochem Cell Biol. 2017 Dec 7.
    Altered muscarinic receptor expression in the cerebral cortex of epileptic rats: Restorative role of Withania somnifera.[Pubmed: 29216436]
    Temporal Lobe Epilepsy involves a sequence of events which can lead to neurotransmitter signalling alterations. Many herbal extracts are considered as alternative therapeutic method for epilepsy management. In the present study, we investigated the effect of Withania somnifera (WS) root extract and Withanolide A (WA) in the management of Temporal Lobe Epilepsy.
    METHODS AND RESULTS:
    Confocal imaging of TOPRO-3 stained cortical sections showed severe damage in epileptic brain. We also observed a reduced antioxidant potential and increased peroxide level in epileptic group. Oxidative stress resulted in the down regulation of CREB, NF-κB and TNF-α with an up regulation of the apoptotic factors Caspase 8, 3 and bax in epileptic group. Epileptic condition also resulted in an increased muscarinic receptor binding and mRNA expression in the cerebral cortex. Withania somnifera and Withanolide A significantly reversed the altered muscarinic receptor expression and reversed the oxidative stress and resultant derailment in cell signalling.
    CONCLUSIONS:
    Thus our studies suggest that Withania somnifera and Withanolide A play an important role in central muscarinic receptor functional balance and activation of antioxidant system in the cerebral cortex of temporal lobe epileptic condition. These findings can be of immense therapeutic significance for epileptic management.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.1249 mL 10.6247 mL 21.2495 mL 42.4989 mL 53.1237 mL
    5 mM 0.425 mL 2.1249 mL 4.2499 mL 8.4998 mL 10.6247 mL
    10 mM 0.2125 mL 1.0625 mL 2.1249 mL 4.2499 mL 5.3124 mL
    50 mM 0.0425 mL 0.2125 mL 0.425 mL 0.85 mL 1.0625 mL
    100 mM 0.0212 mL 0.1062 mL 0.2125 mL 0.425 mL 0.5312 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.
    部分图片展示
    产品名称 产品编号 CAS编号 分子式 = 分子量 位单 联系QQ
    6alpha-氯-5beta-羟基醉茄内酯 A; 6alpha-Chloro-5beta-hydroxywithaferin A CFN91967 52329-20-1 C28H39ClO6 = 507.06 10mg QQ客服:1457312923
    醉茄内酯 B; Withanolide B CFN91963 56973-41-2 C28H38O5 = 454.60 5mg QQ客服:2056216494
    4beta-羟基醉茄内酯 E; 4beta-Hydroxywithanolide E CFN89289 54334-04-2 C28H38O8 = 502.60 5mg QQ客服:2056216494
    Somnifericin; Somnifericin CFN95280 173693-57-7 C28H42O7 = 490.6 5mg QQ客服:1413575084
    2,3-Didehydrosomnifericin; 2,3-Didehydrosomnifericin CFN91969 173614-88-5 C28H40O7 = 488.61 10mg QQ客服:2159513211
    Baimantuoluoside C; Baimantuoluoside C CFN91965 60124-17-6 C28H38O6 = 470.60 5mg QQ客服:1457312923
    (7Alpha,22R)-7,22,27-三羟基-1-氧代麦角甾烷-2,5,24-三烯-26-酸内酯; Daturataturin A aglycone CFN97467 904665-71-0 C28H38O5 = 454.6 5mg QQ客服:1457312923
    Phyperunolide E; Phyperunolide E CFN96990 1198400-52-0 C28H40O9 = 520.61 5mg QQ客服:2056216494
    Viscosalactone B; Viscosalactone B CFN92968 76938-46-0 C28H40O7 = 488.61 5mg QQ客服:1413575084
    2,3-二氢-3-甲氧基醉茄素A; 2,3-Dihydro-3-methoxywithaferin A CFN92965 21902-96-5 C29H42O7 = 502.64 5mg QQ客服:2159513211

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