ChemFaces is a professional high-purity natural products manufacturer.
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1. Reference standards
2. Pharmacological research
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More articles cited ChemFaces products.
Sci Rep. Jan. 2018Horticultural Science2016Inflammation. 2015 Feb 6.J Sci Food Agric. 2017 MarJ Sep Sci. 2017 Dec 27.
Phytomedicine.2018 Jan 1;FEBS Lett.2015 Jan 2;589(1):182-7. Int J Mol Sci.2017 Nov 30;Viruses. 2017 Oct 3;9(10). Curr Eye Res.2018 Jan;
Polytechnic University of Catalonia2016Universite de Bordeaux15 Dec 2017;New Zealand Journal of Forestry Sci.2014, 44:17Tissue and Organ Culture (PCTOC)2016 Jun 28;
Our products had been exported to the following research institutions and universities, And still growing.
Fraunhofer-Institut für Molekul... (Germany)University of Dicle (Turkey)Sanford Burnham Prebys Medical D... (USA)University of Bordeaux (France)
Hamdard University (India)University of Lodz (Poland)Wageningen University (Netherlands)Uniwersytet Medyczny w ?odzi (Poland)
Universit?t Basel (Switzerland)National Cancer Center Research ... (Japan)National Chung Hsing University (Taiwan)
Sequosempervirin B Description
||The heartwood of Sequoia sempervirens
||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: 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.
Sequosempervirin B References Information
Chem Biodivers. 2005 Apr;2(4):497-505.
|Norlignans from Sequoia sempervirens.[Pubmed: 17191998 ]|
|Six new norlignans, named Sequosempervirin B, sequosempervirin C,sequosempervirin D, sequosempervirin E, sequosempervirin F, sequosempervirin G (1-6), together with three known norlignans, agatharesinol (7), agatharesinol acetonide (8), and sugiresinol (9), were isolated from the branches and leaves of Sequoia sempervirens. Their structures were determined mainly by high-resolution mass spectroscopy (HR-MS), and various 1D- and 2D-NMR methods, as well as, in the case of 1, by means of X-ray diffraction. Compound 8 showed anticancer activity towards the A549 non-small-cell lung-cancer cell line (IC50 = 27.1 microM). The acetone extract of S. sempervirens was found to be antifungal towards Candida glabrata (IC50 = 15.98 microg/ml), and both the acetone and MeOH extracts inhibited the proteolytic activity of cathepsin B (IC50 = 4.58 and 5.49 microg/ml, resp.).