葡萄素
Viniferin
产品名称 |
产品编号 |
CAS编号 |
包装 |
QQ客服 |
葡萄素 |
CFN92854 |
253435-07-3 |
1mg |
QQ客服:2056216494 |
葡萄素 |
CFN92854 |
253435-07-3 |
5mg |
QQ客服:2056216494 |
葡萄素 |
CFN92854 |
253435-07-3 |
10mg |
QQ客服:2056216494 |
葡萄素 |
CFN92854 |
253435-07-3 |
20mg |
QQ客服:2056216494 |
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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
Mendel University in Brno (Czech Republic)
Sanford Burnham Medical Research Institute (USA)
Uniwersytet Jagielloński w Krakowie (Poland)
University of Canterbury (New Zealand)
Institute of Bioorganic Chemistry Polish Academy of Sciences (Poland)
Centralised Purchases Unit (CPU), B.I.T.S (India)
Medical University of Gdansk (Poland)
Mahatma Gandhi University (India)
University of Hull (United Kingdom)
Stanford University (USA)
Fraunhofer-Institut für Molekularbiologie und Angewandte ?kologie IME (Germany)
Sri Sai Aditya Institute of Pharmaceutical Sciences and Research (India)
Instituto Politécnico de Bragan?a (Portugal)
Georgia Institute of Technology (USA)
More...
国外学术期刊发表的引用ChemFaces产品的部分文献
Am J Chin Med.2022, 1-20.
Agronomy2023, 13(6), 1435.
J Cell Mol Med.2023, 27(11):1592-1602.
Agriculture.2022, 12(3), 342.
Phytother Res.2022, 10.1002:ptr.7626.
Planta Med.2019, 85(4):347-355
Journal of Ginseng Research2021, 25 November
Int J Mol Sci.2022, 23(5):2796.
Description: |
α-Viniferin has anti-oxidant and anticancer activities, it strongly inhibits the activities of the two CYPs dose dependently. α-Viniferin suppresses the expression of proinflammatory genes iNOS and COX-2 in the early stage of inflammation by inhibiting the Akt/PI3K-dependent NF-κB activation and inhibits the production of proinflammatory mediators NO and PGE2 in the late stage by stimulating Nrf2-mediated HO-1 signaling pathway in LPS-stimulated BV2 microglial cells. ɛ-Viniferin and vincristine can enhance the anti-tumor effects efficiently by inducing HepG2 cell apoptosis. |
Targets: |
NO | PGE | NOS | COX | NF-kB | PI3K | Akt | Nrf2 | HO-1 | P450 (e.g. CYP17) |
In vitro: |
OMICS. 2014 May;18(5):324-34. | Towards novel anti-tumor strategies for hepatic cancer: ɛ-viniferin in combination with vincristine displays pharmacodynamic synergy at lower doses in HepG2 cells.[Pubmed: 24341688] | We investigated the anti-tumor effect of ɛ-Viniferin alone, and the putative synergy of ɛ-Viniferin with vincristine on the growth of HepG2 cells in vitro.
METHODS AND RESULTS:
Growth inhibition and apoptosis induction were determined by MTT assay and annexin V/propidium iodide (PI), respectively. Morphological changes and DNA fragmentation were investigated under electron microscopy and by agarose gel electrophoresis, respectively. The results collectively showed that treating cells with ɛ-Viniferin and vincristine significantly inhibited cell viability at lower doses as compared to each agent applied alone. IC(50) values for ɛ-Viniferin and vincristine were determined as 98.3 and 52.5 μM at 24 h, respectively. IC(50) value of ɛ-Viniferin in combination with vincristine was 15.8+11.25 μM (mean/SD) at 24 h. The viability of cells treated with 17.9 μM vincristine alone for 24 h was 79.62%; it reduced to 26.53% when 25 μM ɛ-Viniferin was added in combination with vincristine (p<0.05). We found that combination of drugs promoted the sensitivity of cells against to vincristine treatment.
CONCLUSIONS:
This study thus suggests that low concentrations of ɛ-Viniferin and vincristine can enhance the anti-tumor effects efficiently by inducing HepG2 cell apoptosis. | Nat Prod Commun. 2015 Jun;10(6):1017-8. | Synthesis of ε-Viniferin Glycosides by Glucosyltransferase from Phytolacca americana and their Inhibitory Activity on Histamine Release from Rat Peritoneal Mast Cells.[Pubmed: 26197540] | METHODS AND RESULTS:
Glycosylation of (+)-ε-viniferin was investigated using glucosyltransferase from Phytolacca americana (PaGT3) as a biocatalyst. (+)-ε-Viniferin was converted by PaGT3 into its 4b- and 13b-β-D-glucosides, the inhibitory activities on histamine release from rat peritoneal mast cells of which were higher than that of (+)-ε-viniferin. |
|
|
1 mg |
5 mg |
10 mg |
20 mg |
25 mg |
1 mM |
2.2022 mL |
11.0108 mL |
22.0216 mL |
44.0432 mL |
55.054 mL |
5 mM |
0.4404 mL |
2.2022 mL |
4.4043 mL |
8.8086 mL |
11.0108 mL |
10 mM |
0.2202 mL |
1.1011 mL |
2.2022 mL |
4.4043 mL |
5.5054 mL |
50 mM |
0.044 mL |
0.2202 mL |
0.4404 mL |
0.8809 mL |
1.1011 mL |
100 mM |
0.022 mL |
0.1101 mL |
0.2202 mL |
0.4404 mL |
0.5505 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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