ChemFaces is a professional high-purity natural products manufacturer.
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According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
|Size /Price /Stock
||10 mM * 1 mL in DMSO / Inquiry||Other Packaging
||*Packaging according to customer requirements(100uL/well, 200uL/well and more), and Container use Storage Tube With Screw Cap
More articles cited ChemFaces products.
J Biol Chem.2014, 289(3):1723-31Nat Prod Commun.2017, 12(5):771-778Arch Pharm Res.2015, 38(6):1080-9World J Mens Health.2019, 10.5534Bull. Natl. Mus. Nat. Sci....2021...Molecules.2015, 20(11):20014-30Antioxidants (Basel).2020, 9(6):544. Free Radic Biol Med.2017, 112:191-199
Biomed Pharmacother.2022, 146:112497.J Agric Food Chem.2016, 64(35):6783-90Academic J of Second Military Med...2018...Plant Physiol Biochem.2019, 144:355-364Phytomedicine.2018, 41:62-66Oncotarget.2016, 8(51):88386-88400Food Chem.2020, 327:126992.Phytomedicine.2021, 93:153796.
Mol Neurobiol.2021, 58(8):3665-3676. Chemistry of Vegetable Raw Materi...2019...Agronomy 2021, 11(3),502.Pharmaceuticals (Basel). ...2021...Front Pharmacol.2021, 12:635510.Arch Biochem Biophys.2018, 644:93-99Antioxidants (Basel).2020, 9(7):581.
Our products had been exported to the following research institutions and universities, And still growing.
Universidad de Antioquia (Colombia)University of Hertfordshire (United Kingdom)Lodz University of Technology (Poland)Korea Food Research Institute(K... (Korea)
University of Wollongong (Australia)Complutense University of Madrid (Spain)Georgia Institute of Technology (USA)Imperial College London (United Kingdom)
University of Brasilia (Brazil)Indian Institute of Science (India)John Innes Centre (United Kingdom)
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1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
Food Chem.2020, 327:126992.Phytomedicine.2018, 47:48-57Oxid Med Cell Longev.2021, 2021:4883398.Int J Mol Sci.2018, 19(9):E2601Environ Toxicol.2020, doi: 10.1002Arch Biochem Biophys.2020, 687:108363.Am J Chin Med.2015, 30:1-22Evid Based Complement Alternat Med.2017, 2017:1583185Evid Based Complement Alternat Med.2016, 2016:4357656Molecules.2018, 23(9):E2121
Related Screening Libraries
|| Cuniloside B shows anti-leishmanial activity.|
|Pharm Biol. 2012 Jul;50(7):823-7. |
|Terpenoidal constituents of Eucalyptus loxophleba ssp. lissophloia.[Pubmed: 22468852]|
|Eucalyptus has been a source of a number of biologically active compounds. The anti-leishmanial activity of terpenoids from Eucalyptus loxophleba (Benth.) ssp. lissophloia (Myrtaceae) has not yet been investigated.
Isolation of the terpenoidal constituents for evaluation of in vitro anti-leishmanial activity against the Leishmania donovani (Dd8 strain) promastigotes.
METHODS AND RESULTS:
The chloroform-methanol (8:2) extract of dried leaves of Eucalyptus loxophleba was used to isolate terpenoidal constituents employing solvent partitioning, column chromatography and preparative high performance liquid chromatography and characterized from spectral data. The anti-leishmanial activity of the isolated compounds was tested in vitro using an Alamar blue assay against a culture of L. donovani (Dd8 strain) promastigotes.
Two new naturally occurring triterpenes, named loxanic acid and 3-acetyl loxanic acid together with four known ursane triterpenoids and one bis-monoterpene glycoside, Cuniloside B isolated from the leaves showed anti-leishmanial activity (IC(50) 133 to 235 μM) against the promastigotes of the tested strain.
The terpenes isolated from the leaves of E. loxophleba showed moderate anti-leishmanial activity.
Cuniloside B Description
||The herbs of Eucalyptus microcory
||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: 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.
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.IF=36.216(2019)PMID: 29328914
Cell Metab. 2020 Mar 3;31(3):534-548.e5. doi: 10.1016/j.cmet.2020.01.002.IF=22.415(2019)PMID: 32004475
Mol Cell. 2017 Nov 16;68(4):673-685.e6. doi: 10.1016/j.molcel.2017.10.022.IF=14.548(2019)PMID: 29149595
ACS Nano. 2018 Apr 24;12(4): 3385-3396. doi: 10.1021/acsnano.7b08969.IF=13.903(2019)PMID: 29553709
Nature Plants. 2016 Dec 22;3: 16206. doi: 10.1038/nplants.2016.205.IF=13.297(2019)PMID: 28005066
Sci Adv. 2018 Oct 24;4(10): eaat6994. doi: 10.1126/sciadv.aat6994.IF=12.804(2019)PMID: 30417089
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.
|Carbohydr Res. 2010 Sep 23;345(14):2079-84. |
|Synthesis of the monoterpenoid esters cypellocarpin C and cuniloside B and evidence for their widespread occurrence in Eucalyptus.[Pubmed: 20708173]|
METHODS AND RESULTS:
Short syntheses of Cuniloside B and cypellocarpin C, (+)-(R)-oleuropeic acid-containing carbohydrates, are reported. Also disclosed are syntheses of the noreugenin glycosides, undulatoside A and corymbosins K(1) and K(2). Leaf extracts of 28 diverse eucalypts revealed Cuniloside B to be present in all, and cypellocarpin C to be present in most, of the species examined.
The widespread occurrence of these carbohydrate monoterpenoid esters supports their roles in essential oil biosynthesis or mobilization from sites of synthesis to secretory cavity lumena.