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According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
|Size /Price /Stock
||10 mM * 1 mL in DMSO / Inquiry||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.
FEBS Lett.2015, 589(1):182-7Food and Agriculture Org. Of the ...2019...Int J Pharmacol2020, 16:1-9Int J Mol Sci.2021, 22(8):4211.Dicle Tip Dergisi2020, 47(2),423-430.Korean J. Medicinal Crop Sci....2021...ACS Omega.2022, 7(44):40009-40020.Int J Mol Sci.2018, 19(9):E2681
Aquaculture2017, 481:94-102Cells.2021, 10(10):2633.Biomedicines.2021, 9(8):954.J of L. Chroma.&Related Tech...2017...Korean Herb. Med. Inf....2021...Molecules.2021, 26(9):2765. Phytochemistry.2017, 141:162-170Food Science and Biotechnology...2015...
J Food Composition and Analysis...2022...Asian J Beauty Cosmetol...2020...Molecules.2022, 27(4):1412. JAOCS2021, 98(7):779-794.JEJU National University2022, 24032.Neurotox Res.2020, 38(1):163-174.Phytochemistry Letters2021, 43:80-87.
Our products had been exported to the following research institutions and universities, And still growing.
Mahatma Gandhi University (India)Universitas islam negeri Jakarta (Indonesia)Medical University of Gdansk (Poland)Charles University in Prague (Czech Republic)
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1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
Molecules.2019, 24(6):E1155Molecules2022, 27(3),1140.Int J Mol Sci.2019, 20(8):E1855Molecules.2016, 21(6)New Zealand J. Forestry Sci.2014, 44:17J Chromatogr B Analyt Technol Biomed Life Sci.2019, 1126-1127:121743Oncotarget.2016, 8(51):88386-88400Am J Chin Med.2022, 1-20.Evid Based Complement Alternat Med.2021, 2021:5319584.LWT2021, 147:111620.
Related Screening Libraries
||Torachrysone shows promising antioxidant activity. Torachrysone, toralactone , aloe-emodin, rhein and emodin show noticeable antibacterial effects on four strains of methicillin-resistant Staphylococcus aureus with a minimum inhibitory concentration of 2-64 micrograms/ml.
|Chem. Pharm. Bull.(Tokyo).,1999, 47(8): 1121-7. |
|Phenolic constituents of Cassia seeds and antibacterial effect of some naphthalenes and anthraquinones on methicillin-resistant Staphylococcus aureus.[Pubmed: 10478467]|
|Thirteen phenolic glycosides including six new compounds were isolated from seeds of Cassia tora (Leguminosae).
METHODS AND RESULTS:
The structures of the new compounds, rubrofusarin triglucoside (7), nor-rubrofusarin gentiobioside (9), demethylflavasperone gentiobioside (10), Torachrysone gentiobioside (11), Torachrysone tetraglucoside (12) and Torachrysone apioglucoside (13), were elucidated on the basis of spectroscopic and chemical evidence. The effects of the phenolic glycosides, their aglycones and several other compounds structurally related to them on Escherichia coli K12, Pseudomonas aeruginosa PAO1 and some strains of Staphylococcus aureus were then examined.
Among them, Torachrysone (15), toralactone (16), aloe-emodin (18), rhein (19) and emodin (20) showed noticeable antibacterial effects on four strains of methicillin-resistant Staphylococcus aureus with a minimum inhibitory concentration of 2-64 micrograms/ml. On the other hand, the phenolic compounds tested did not show strong antibacterial effects on E. coli and P. aeruginosa.
||The seeds of Cassia obtusifolia
||Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, 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.
|Molecules. 2014 Aug 4;19(8):11453-64. |
|An unusual piceatannol dimer from Rheum austral D. Don with antioxidant activity.[Pubmed: 25093985]|
METHODS AND RESULTS:
A novel dimer of piceatannol glycoside, named rheumaustralin (1) was isolated from the underground parts of the ethnomedicinal plant Rheum austral (Polygonaceae) collected from Tibet together with 17 known compounds, including rheumin (2), 2,5-dimethyl-7-hydroxychromone (3), 2,5-dimethylchromone-7-O-β-D-glucopyranoside (4), 7-hydroxy-2-(2'-hydroxypropyl)-5-methylchromone (5), Torachrysone (6) Torachrysone-8-O-β-D-glucopyranoside (7), 4-(4'-hydroxyphenyl)-2-butanone-4'-O-β-D-glucopyranoside (8), amabiloside (9), N-trans-feruloyl tyramine (10), chrysophanol (11), aloe-emodin (12), emodin (13), physcion (14), physcion-1-O-β-D-glucopyranoside (15), emodin-8-O-β-D-glucopyranoside (16), D-catechin (17) and gallic acid (18).
Their structures were determined by combined spectroscopic methods and by comparison of their spectral data with those reported in literature. Compounds 1-10 were tested for their ability to scavenge 1, 1-diphenyl-2-picrylhydrazyl (DPPH) radical.
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