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|Size /Price /Stock
||10 mM * 1 mL in DMSO / $251.2 / In-stock||Other Packaging
||*Packaging according to customer requirements(100uL/well, 200uL/well and more), and Container use Storage Tube With Screw Cap
More articles cited ChemFaces products.
Phytomedicine.2020, 79, 153351Cancers (Basel).2023, 15(1):37. Plos One.2020, 10.1371Histol Histopathol.2022, 18518.Antioxidants2022, 11(2),234.Chem Pharm Bull (Tokyo)....2017...Plants (Basel).2023, 12(1):163.Vietnam J. Chemistry2022, 60(2):211-222
Mol Cells.2015, 38(9):765-72Int J Mol Sci.2022, 23(13):7115. In Vitro Cellular & Developmental...2021...Evid Based Complement Alternat Me...2021...Analytical Letters 2021, 54(4).Korean J Dent Mater2020, 47(2):63-70.Food Chem.2017, 228:301-314J Sep Sci.2022, 45(18):3556-3566.
J Appl Biol Chem2021, 64(3):245-251.Sci Rep. 2017, 8207(7)Biochem Biophys Res Commun....2018...Int J Mol Sci.2018, 19(9):E2601Asian Journal of Chemistry...2014...Korean J Dent Mater.2018, 45(2):139-146Antioxidants (Basel).2020, 9(4):326.
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Plos One.2020, 10.1371Processes2021, 9(1), 153;Int. J. Mol. Sci.2022, 23(14),7699; Journal of Ginseng Research2021, 3 June.Antioxidants (Basel).2019, 8(8):E307Saf Health Work.2019, 10(2):196-204J Ethnopharmacol.2020, 260:112988.Acta Chromatographica2021, 00960.Toxicol In Vitro.2022, 81:105346. J Biochem Mol Toxicol.2020, 34(7):e22489.
Related Screening Libraries
|| Quercetin 3-O-(6''-galloyl)-beta-D-galactopyranoside can effectively induce apoptosis via p53, MAPKs and the mitochondrial apoptotic pathways. |
||p53 | MAPK|
Quercetin 3-O-(6''-galloyl)-beta-D-galactopyranoside Description
||The herbs of Hypericum perforatum L.
||DMSO, Pyridine, Methanol, Ethanol, etc.
||Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
Need more advice on solubility, usage and handling? Please email to: firstname.lastname@example.org
||The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
ChemFaces New Products and Compounds
Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals
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
Calculate Dilution Ratios(Only for Reference)
* 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.
|Food Funct. 2015 Dec;6(12):3746-59. |
|Bioactive compounds of Eriocaulon sieboldianum blocking proliferation and inducing apoptosis of HepG2 cells might be involved in Aurora kinase inhibition.[Pubmed: 26369427 ]|
|Eriocaulon sieboldianum (Sieb. & Zucc. ex Steud.) is an edible and medicinal plant used in traditional Chinese medicine. Often in combination with other herbs, it is processed into healthcare beverages for expelling wind-heat, protecting eyes, and reducing blood lipids. Besides, its water decoction together with other herbs has been utilized to treat cancer in China. However, the active ingredients and the precise cellular mechanisms of E. sieboldianum remain to be elucidated.
The Aurora kinase family plays critical roles in the regulation of cell division and has attracted great attention to the identification of small-molecule Aurora kinase inhibitors for potential treatment of cancer.
METHODS AND RESULTS:
A molecular docking study was employed for docking of the most bioactive compounds. Hispidulin (HPDL) and quercetin-3-O-(6''-O-galloyl)-β-D-galactopyranoside (Quercetin 3-O-(6''-galloyl)-beta-D-galactopyranoside, QGGP) were singled out as potent inhibitors of Aurora kinase. Their inhibitory activity towards Aurora kinase was further confirmed by the obvious decrease in autophosphorylation of Aurora-A (Thr288) and Aurora-B (Thr232). Moreover, the induction of cell cycle arrest in HepG2 cells and the suppressed phosphorylation of histone H3 were also consistent with the inhibition of Aurora kinase. The data indicate that the E. sieboldianum extract and its two active compounds, HPDL and QGGP, could effectively induce apoptosis via p53, MAPKs and the mitochondrial apoptotic pathways.
These findings could improve the understanding and enhance the development of drugs based on E. sieboldianum and raise its application value in anticancer therapy or prevention. In addition, our results indicated that Aurora kinase might be a novel target of HPDL and QGGP.
|Yao Xue Xue Bao. 2010 Mar;45(3):334-7. |
|One new galloyl glycoside from fresh leaves of Psidium guajava L.[Pubmed: 21348423]|
|To investigate the chemical constituents of Psidium Guajava L, the EtOH/H2O extract of the fresh leaves was subjected to various chromatography. |
METHODS AND RESULTS:
Five constituents with galloyl moiety were isolated and elucidated as 1-O-(1, 2-propanediol)-6-O-galloyl-beta-D-glucopyranoside (1), gallic acid (2), ellagic acid (3), ellagic acid-4-O-beta-D-glucopyranoside (4) and Quercetin 3-O-(6''-galloyl)-beta-D-galactopyranoside (5) by spectroscopic methods, including 2D NMR and HR-ESI-MS spectrometry as well as by comparison with published data.
Compounds 4 and 5 were obtained from P. guajava for the first time, and compound 1 is a new polyhydroxyl compound.
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