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.
Mol Cells.2015 Sep 30;38(9):765-72.Pharmacological Reports31 May 2017Oncology LettersJan. 25, 2018;Cell Physiol Biochem.2017;43(4):1425-1435.JPCMarch 16, 2017
J Sci Food Agric. 2017 Jul 22. Separation Science and Technology2016 Mar,23Int J Mol Sci. 2017 Dec 21;Journal of Functional FoodsFeb. 2018;Anal Bioanal Chem.2018 Feb;
Free Radic Biol Med.2017 Nov;FEBS Lett.2015 Jan 2;589(1):182-7. Front Pharmacol. 2016 Nov 30J Breast Cancer2015 Jun;18(2):112-118.
Our products had been exported to the following research institutions and universities, And still growing.
Universidade de Franca (Brazil)Istanbul University (Turkey)University of Malaya (Malaysia)Universita' Degli Studi Di Cagli... (Italy)
Amity University (India)Kitasato University (Japan)University of Wisconsin-Madison (USA)University of Perugia (Italy)
University of Madras (India)S.N.D.T. Women's University (India)Celltrion Chemical Research Inst... (Korea)
|| Eucalyptolic acid is a natural product from Eucalyptus globulus.|
Eucalyptolic acid Description
||The branches of Eucalyptus globulus
||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.2017.12.030PMID: 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.
|Planta Medica, 1997 , 63 (01) :47-50. |
|Isolation and Structural Elucidation of Acylated Pentacyclic Triterpenoids from the Leaves of Eucalyptus camaldulensis var. obtusa[Reference: WebLink]|
METHODS AND RESULTS:
Ten pentacyclic triterpenoids including two new constituents, eucalyptic acid and Eucalyptolic acid, and eight known compounds (ursolic acid lactone, betulinic acid, oleanolic acid, ursolic acid, 3 beta-O-cis-p-coumaroylalphitolic acid, alphitolic acid, 3 beta-O-trans-p-coumaroylalphitolic add, and 3 beta-O-trans-p-coumaroylmaslinic acid) have been isolated from the fresh and uncrushed leaves of Eucalyptus camaldulensis var. obtuse. Their structures were elucidated through detailed 1D and 2D NMR studies. The new natural products were characterized as 2 alpha-hydroxy-3 beta-E-feruloyloxy-lup-20(29)-en-28-oic acid and 2 alpha-hydroxy-3 beta-E-feruloyloxy-olean-12-en-28-oic acid, respectively.
Except for oleanolic acid, all the known compounds are hitherto unreported from this plant. This is the first report of the isolation of 2-oxygenated 3-O-acylated triterpenoids from Eucalyptus genus.