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16-O-Acetylpolyporenic acid C
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More articles cited ChemFaces products.
Pharmacological Reports31 May 2017International Journal of Mol. Med.2015 Mar 6.Molecules 2016, 21(6)2016 Jun 22;21(6). Int J Mol Sci. 2017 May 11;Cell Physiol Biochem. 2017;44(4);
J Sep Sci. 2017 Dec 27.Phytother Res.2018 Jan 29.Universidade Estadual Paulista2017-02-19Jour. of Stored Pro & Postharvest Res.March 2016Plant Cell, (PCTOC)05 November 2016
Am J Chin Med.2016;44(8)Int J Mol Sci.2017 Nov 30;Tumour Biol.2015 Apr 12.Chem Pharm Bull (Tokyo).2017;65(9)
Our products had been exported to the following research institutions and universities, And still growing.
Deutsches Krebsforschungszentrum (Germany)University of Wollongong (Australia)University of Pretoria (South Africa)Macau University of Science and ... (China)
University of Illinois at Chicago (USA)Molecular Biology Institute of B... (Spain)Monash University (Australia)Uniwersytet Jagielloński w Krak... (Poland)
Washington State University (USA)Monash University Malaysia (Malaysia)Kazusa DNA Research Institute (Japan)
16-O-Acetylpolyporenic acid C Description
||The herbs of Daedalea dickinsii
||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.
16-O-Acetylpolyporenic acid C References Information
Phytochemistry. 2000 Aug;54(8):757-62.
|Constituents of the fungi Daedalea quercina and Daedaleopsis confragosa var. tricolor.[Pubmed: 11014261]|
|Phytochemical examination of solvent extracts of the wood-rotting fungi Daedalea quercina and Daedaleopsis confragosa var. tricolor led to the isolation of five new triterpene derivatives and some known fungal constituents. All structures were identified by one- and two-dimensional NMR spectroscopy and mass spectrometry. From Daedalea quercina, the new natural products 16-O-Acetylpolyporenic acid C, 16alpha-acetoxy-24-methylene-3-oxolanost-8-en-21-oic acid, (+)-24-methylene-3,23-dioxolanost-8-en-26-oic acid, (+)-3beta,12beta-dihydroxy-24-methyl-23-oxolanost-8-en-26-oi c acid and 12beta,23-epoxy-3alpha,23-dihydroxy-24-methyllanost-8- en-26-oic acid could be isolated. From Daedaleopsis confragosa var. tricolor, the compounds 3alpha-carboxyacetoxyquercinic acid, 3alpha-carboxyacetoxy-24-methylene-23-oxolanost-8-en-2 6-oic acid and 5alpha,8alpha-epidioxyergosta-6,22-dien-3beta-ol were identified. These are the first described triterpene derivatives isolated from this fungus.