ChemFaces is a professional high-purity natural products manufacturer.
Product Intended Use
1. Reference standards
2. Pharmacological research
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More articles cited ChemFaces products.
Arch Toxicol. 2017 Mar 20. Separation Science and Technology2016 Mar,23Onco Targets Ther. 2017 Jul 13;Molecules. 2017 Feb 8;Int. Conference on Med. Sci. and Bio.2017;
Universidade Estadual Paulista2017-02-19Tumour Biol.2015 Apr 12.Free Radic Biol Med.2016 Jun 25;97:307-319. Br J Pharmacol.2018 Mar;Am J Chin Med.2016;44(8)
Industrial Crops and ProductsFeb. 2018;J Pharm Biomed Anal. 2017 Jun 5;Naunyn Schmiedebergs Arch Pharmacol. 2017 Jul 21. Cytotechnology. 2017 Apr 3.
Our products had been exported to the following research institutions and universities, And still growing.
The Institute of Cancer Research (United Kingdom)Center for protein Engineering (... (Belgium)Heidelberg University (Germany)John Innes Centre (United Kingdom)
University of Minnesota (USA)Kyung Hee University (Korea)Subang Jaya Medical Centre (Malaysia)Kyushu University (Japan)
Korea Food Research Institute(KF... (Korea)Korea Institute of Oriental Medi... (Korea)Universiti Sains Malaysia (Malaysia)
||1. Isosalvianolic acid C exhibits more potent activity than probucol except for salvianolic acid F .|
Isosalvianolic acid C Description
||The herbs of Tournefortia sarmentosa.
||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: email@example.com
||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.
Recent 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.PMID: 29328914
Mol Cell. 2017 Nov 16;68(4):673-685.e6. doi: 10.1016/j.molcel.2017.10.022.PMID: 29149595
Scientific Reports 2017 Dec 11;7(1):17332.doi: 10.1038/s41598-017-17427-6.PMID: 29230013
Molecules. 2017 Oct 27;22(11). pii: E1829.doi: 10.3390/molecules22111829.PMID: 29077044
J Cell Biochem. 2018 Feb;119(2):2231-2239.doi: 10.1002/jcb.26385. PMID: 28857247
Phytomedicine. 2018 Feb 1;40:37-47. doi: 10.1016/j.phymed.2017.12.030.PMID: 29496173
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.
Isosalvianolic acid C References Information
J Nat Prod. 2002 May;65(5):745-7.
|Anti-lipid-peroxidative principles from Tournefortia sarmentosa.[Pubmed: 12027757]|
|Using the inhibition of Cu(2+)-induced low-density-lipoprotein (LDL) peroxidation to direct fractionation, four new benzenoids, tournefolal (1), tournefolic acids A (2) and B (3), and B ethyl ester (4), together with salvianolic acid A (5), Isosalvianolic acid C (6), lithospermic acid (7), salvianolic acid F (8), and rosmarinic acid (9), were isolated from the stems of Tournefortia sarmentosa. The structures of the new compounds 1-4 were elucidated on the basis of spectral and chemical methods. Furthermore, the anti-LDL-peroxidative activity of the isolated compounds was determined. All isolated compounds exhibited more potent activity than probucol except for salvianolic acid F (8).