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|Size /Price /Stock
||10 mM * 1 mL in DMSO / Inquiry||Other Packaging
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More articles cited ChemFaces products.
University of Limpopo2016, 1777J Drug Target.2016, 24:1-28Front Pharmacol.2016, 7:460Universidade Estadual Paulista...2017...BMC Complement Altern Med....2017...J Ethnopharmacol.2017, 206:73-77J Ethnopharmacol.2017, 209:305-316Food Chem.2017, 228:301-314
LWT-Food Science and Technology...2017...Viruses.2017, 9(10)Exp Parasitol.2018, 194:67-78Molecules.2018, 23(7):E1659J of Health Science and Alternati...2019...Nutrients.2019, 11(11):E2694BMC Complement Altern Med....2019...Chin J Pharm Anal.2019, 39(7):1217-1228
Korean Journal of Pharmacognosy....2019...Journal of Functional Foods...2019...Genes Genomics.2020, 10.1007United States Patent Application...2020...Biochem Pharmacol.2020, 178:114083Chinese Journal of Hospital Pharm...2020...Horticulture Research2020, 7:111.
Our products had been exported to the following research institutions and universities, And still growing.
Chulalongkorn University (Thailand)Monash University Malaysia (Malaysia)Michigan State University (USA)Centrum Menselijke Erfelijkheid (Belgium)
Universiti Kebangsaan Malaysia (Malaysia)Yale University (USA)Max Rubner-Institut (MRI) (Germany)University of Bonn (Germany)
Technical University of Denmark (Denmark)Chinese University of Hong Kong (China)Copenhagen University (Denmark)
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J Neuroinflammation.2020, 17(1):75.Planta Med.2016, 82(13):1208-16J. of Med. Plant Research.2013, 90-151Agronomy2020, 10(3),388.Pharmacognosy Journal.2020, 12(2), p232-235.Molecules.2020, 25(3):734J Chromatogr B Analyt Technol Biomed Life Sci.2018, 1080:27-36PLoS One.2020, 15(2):e0220084.Toxins (Basel).2020, 12(4):210. J Nat Med.2017, 71(2):380-388
Related Screening Libraries
|| Nodosin has anti-inflammatory function of Nodosin via inhibition of IL-2. Nodosin perfusion provides a potential protective effect through inducing HO-1 expression to attenuate ischemia/reperfusion injury in liver transplantation. |
||IL Receptor | HO-1|
|Am J Chin Med. 2010;38(1):127-42. |
|Anti-inflammatory function of Nodosin via inhibition of IL-2.[Pubmed: 20128050]|
|In order to explore the anti-inflammatory effects of Nodosin from Isodon serra, a traditional Chinese herb medicine, mouse T lymphocytes were incubated with Nodosin.|
METHODS AND RESULTS:
In the current study, Nodosin suppressed the overproduction of the T lymphocytes; moreover, cell mitosis cycle was modulated by interfering with DNA replication in G1 stages via inhibition of IL-2 cytokine secretion at the mRNA level by Nodosin.
Interestingly, Xylene-induced mouse tumescence model results suggested Nodosin depressed the murine ear-swelling extent and the level of IL-2 in the blood serum.
Finally, Nodosin possessed significant anti-inflammatory effects and is a potential candidate for further clinical trial.
||The herbs of Isodon serra
||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.
|J Gastroenterol Hepatol. 2012 Apr;27(4):832-40. |
|Preconditioning donor liver with Nodosin perfusion lessens rat ischemia reperfusion injury via heme oxygenase-1 upregulation.[Pubmed: 22098251]|
|Ischemia reperfusion injury (IRI) remains a major cause of graft injury, dysfunction and even failure post-transplantation. Heme oxygenase 1 (HO-1) has been found to be an attractive target for anti-inflammatory therapies and a potential candidate responsible for cell injury. The objective of this study was to investigate whether preconditioning the donor liver with Nodosin perfusion upregulates HO-1 and then lessens IRI in rat models.
METHODS AND RESULTS:
Wistar rats were divided into four groups: experimental group, control group, positive control group and negative control group in which the donor liver was preconditioned with Nodosin, lactated ringer's solution, cobalt protoporphyrin and zinc protoporphyrin perfusion, respectively. We measured HO-1 expression and enzyme activity in rat livers of each group ex vivo at 0, 1 and 2 h after perfusion. At 1 h after perfusion, donor livers of Wistar rats were transplanted into Sprague-Dawley rats orthotopically. Serum transaminase levels, degree of cell apoptosis and Suzuki's score were used to assess ischemia/reperfusion injury in recipients at 24 h after transplantation.
Ex vivo, donor liver preconditioning with Nodosin perfusion induced HO-1 expression and enzyme activity significantly, compared with the control group (P < 0.05). In vivo, serum transaminase levels, cell apoptosis degree and Suzuki's score of representative recipients in the Nodosin group were lower than that in the control group (P < 0.05). Preconditioning with Nodosin perfusion induced HO-1 protein mainly in Kupffer cells.
This study suggests that preconditioning with Nodosin perfusion provides a potential protective effect through inducing HO-1 expression to attenuate ischemia/reperfusion injury in liver transplantation.