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More articles cited ChemFaces products.
J. Acta Agr. Scandinavica17 Apr 2017J Sep Sci. 2017 Dec 27.Journal of Agricultural Science2015 Sep 15Preprints.25 Dec. 2017;J of L. Chroma. & Related Tech2017 Apr 21;
Chemistr of plant2016021195US20170000760 A1Jan 5, 2017Integr Med Res.2017 Dec;Korean J. of Food Sci. and TechApril 2016Jou. of Agromedicine and Med. Sci.2018;
Sci Rep. 2017 Jun 12;Mol Cell2017 Nov 16;Evid Based Complement Alternat Med. 2017:6360836.Tissue and Organ Culture (PCTOC)2016 Jun 28;
Our products had been exported to the following research institutions and universities, And still growing.
Monash University (Australia)Siksha O Anusandhan University (India)Sri Ramachandra University (India)Harvard University (USA)
Pennsylvania State University (USA)VIB Department of Plant Systems ... (Belgium)Universitas Airlangga (Indonesia)University of Brasilia (Brazil)
Sanford Burnham Prebys Medical D... (USA)Guangzhou Institutes of Biomedic... (China)Macau University of Science and ... (China)
|| Ganoderic acid L is a natural product from the fruiting body of the fungus Ganoderma lucidum (Reishi).|
Ganoderic acid L Description
||The fruit body of Ganoderma lucidum.
||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.
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.2017.12.030PMID: 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.
|Journal of the Agricultural Chemical Society of Japan, 1986, 50(3):809-811. |
|New Terpenoids, Ganolucidic Acid D, Ganoderic Acid L, Lucidone C and Lucidenic Acid G, from the Fungus Ganoderma lucidum.[Reference: WebLink]|
|The fruiting body of the fungus Ganoderma lucidum (Reishi) has attracted much attention as a folk medicine, and some of its components have been elucidated. |
METHODS AND RESULTS:
We have also reported several bitter terpenoids and related compounds from the fungus.1~9) The naming of lucidenic acids is a little confused, so we now designate our lucidenic acids D and E2) as Dx and El5 and Kikuchi's7) as D2 and E2, respectively. Recently, we have isolated four new terpenoids, ganolucidic acid D (1), methyl ganoderate L (2a), lucidone C (3) and methyl lucidenate G (4a). Ganolucidic acid D (1) has a allylic alcohol group in the side chain and can the mycelial components10) and terpenoids of the fruiting body. On the other hand, Ganoderic acid L (2), which has a hydroxyl group at C-20, can be a possible precursor of lucidone C (3).
Among the lucidenic acids, lucidenic acid G (4) is unique in having a hydroxyl group at C-26.