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Beta-Dimorphecolic acid (9(S)-HODE)
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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 / $222.6 / In-stock||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.
Chem Biol Interact.2020, 328:109200.Int J Mol Sci.2017, 18(12)Molecules.2020 ,25(16):3697.Int J Med Sci.2020, 17(5):626-631J Agric Food Chem.2015, 63(44):9869-78Appl. Sci.2020, 10(20), 7323.Mol Pharm.2017, 14(9):3164-3177Toxins (Basel).2021, 13(12):898.
Viruses.2017, 9(10)Korea Institute of Oriental Medic...2020...Food Chem.2021, 360:130063.LWT-Food Sci Technol2020, 109163Journal of Life Science2018, 917-922Phytother Res.2019, 33(5):1490-1500Toxicological Research...2020...Journal of Analytical Chemistry...2017...
J Ethnopharmacol.2016, 192:370-381Environ Toxicol.2019, 34(12):1354-1362Molecular & Cellular Toxicology...2017...Scientific World Journal....2014...BMC Microbiol.2019, 19(1):78Int Immunopharmacol....2021...Antioxidants (Basel).2019, 8(8):E307
Our products had been exported to the following research institutions and universities, And still growing.
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Beta-Dimorphecolic acid (9(S)-HODE)
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1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
Journal of Physiology & Pathology in Korean Medicine.2018, 32(2): 106-112J of Apicultural Research2020, 10.1080Industrial Food Engineering2015, 19(4):408-413J of Essential Oil Research2019, 1677272Pharmacol Rep.2020, 72(2):472-480.Biomolecules.2019, 9(11):E696Front Plant Sci.2020, 11:630.South African J of Botany2020, 135:50-57Hum Exp Toxicol.2017, 36(11):1169-1176Biosci Rep.2018, 38(4)
Related Screening Libraries
|Pharmacogn Mag . Jul-Sep 2015;11(43):477-85 |
|A direct protein kinase B-targeted anti-inflammatory activity of cordycepin from artificially cultured fruit body of Cordyceps militaris[Pubmed: 26246722]|
|Background: Cordyceps militaris is one of well-known medicinal mushrooms with anti-inflammatory, anti-cancer, anti-diabetic, and anti-obesity activities.
Objective: The objective of the following study is to isolate chemical components from the ethanol extract (Cm-EE) from Cordyceps militaris and to evaluate their anti-inflammatory activities.
Materials and methods: Column chromatographic separation was performed and anti-inflammatory roles of these compounds were also examined by using NO production and protein kinase B (AKT) activity assays.
Results: From Cm-EE, 13 constituents, including trehalose (1), cordycepin (2), 6-hydroxyethyladenosine (3), nicotinic amide (4), butyric acid (5), β-dimorphecolic acid (6), α-dimorphecolic acid (7), palmitic acid (8), linoleic acid (9), cordycepeptide A (10), 4-(2-hydroxy-3-((9E,12E)-octadeca-9,12-dienoyloxy)propoxy)-2-(trimethylammonio)butanoate (11), 4-(2-hydroxy-3-(palmitoyloxy)propoxy)-2-(trimethylammonio)butanoate (12), and linoleic acid methyl ester (13) were isolated. Of these components, compound 2 displayed a significant inhibitory effect on NO production in lipopolysaccharide (LPS)-activated RAW264.7 cells. Furthermore, this compound strongly and directly suppressed the kinase activity of AKT, an essential signalling enzyme in LPS-induced NO production, by interacting with its ATP binding site.
Conclusion: C. militaris could have anti-inflammatory activity mediated by cordycepin-induced suppression of AKT.|
Beta-Dimorphecolic acid (9(S)-HODE) Description
||The herbs of Piper cubeba
||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.
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.
|ChemInform 63(32):7624-7633 |
|Enantioselective syntheses of (-)-pinellic acid, α- and β-dimorphecolic acid[Reference: WebLink]|
|An efficient enantioselective convergent approach for the synthesis of (−)-pinellic acid 1, α- and β-dimorphecolic acid (2 and 3) from 1,9-nonane diol is described. The synthetic strategy features Sharpless asymmetric hydroxylation, Sonogashira coupling and Birch reduction.|