ChemFaces is a professional high-purity natural products manufacturer.
Product Intended Use
1. Reference standards
2. Pharmacological research
Citing Use of our Products
How to Order
Orders via your E-mail:
1. Product number / Name / CAS No.
2. Delivery address
3. Ordering/billing address
4. Contact information
Sent to Email: firstname.lastname@example.org
Order & Inquiry & Tech Support
Address: No. 83, CheCheng Rd., WETDZ, Wuhan, Hubei 430056, PRC
Delivery & Payment method
1. Usually delivery time: Next day delivery by 9:00 a.m. Order now
2. We accept: Wire transfer & Credit card & Paypal & Western Union
* Packaging according to customer requirements(5mg, 10mg, 20mg and more). We shipped via FedEx, DHL, UPS, EMS and others courier.
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.
Pharmacogn Mag.2015, 11:S585-91Tumour Biol.2015, 36(12):9385-93Pharm Biol.2017, 55(1):360-366Viruses.2017, 9(10)Drug Test Anal.2018, 10(10):1579-1589Korean J of Medicinal Crop Scienc...2018...Nat Prod Sci.2018, 24(2):109-114Korean J Environ Agric....2018...
The Journal of Agromedicine and M...2018...J Sep Sci.2018, 41(9):1938-1946Pharmacognosy Journal...2019...Biomed Pharmacother.2019, 116:108987Int J Immunopathol Pharmacol....2019...Sci Rep.2019, 9(1):4646Food Funct.2020, 10.1039Appl. Sci.2020, 10(23), 8729
Front Pharmacol.2020, 11:683.Pharmaceuticals (Basel)....2020...Oncol Lett.2020, 20(4):122.Int J Mol Sci.2020, 21(24):9369.Chemistry of Natural Compounds...2020...J Chromatogr Sci.2020, 58(6):485-493.Environ Toxicol.2020, doi: 10.1002
Our products had been exported to the following research institutions and universities, And still growing.
University of Madras (India)Shanghai University of TCM (China)Sri Sai Aditya Institute of Pha... (India)University of Padjajaran (Indonesia)
University of Wollongong (Australia)University of Otago (New Zealand)University of British Columbia (Canada)Griffith University (Australia)
Wageningen University (Netherlands)University of Maryland (USA)Universidad de Antioquia (Colombia)
Inquire / Order:
1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
J Med Food.2016, 19(12):1155-1165J Sep Sci.2018, 41(11):2488-2497J Med Food.2019, 22(10):1067-1077Chemistry of Natural Compounds2018, 54(3):572–576Chem Biol Interact.2019, 315:108910Food Res Int.2020, 133:109130.Journal of Apiculture2019, 34(2):131-136BMC Complement Altern Med.2016, 16:213J Insect Sci.2020, 20(5):18. Pharmaceutical Chemistry Journal2019, 52(12):986-991
Related Screening Libraries
|| Astragaloside may protect against brain contusion and neuronal apoptosis after TBI by attenuating microglia activation in male rats. Astragalosides-induced apoptosis in NB4 cells may be associated with down-regulation of the expression of BCL-2 and NF-κB, finally the relative activity of caspase-3 activated. Astragaloside has several pharmacological actions on cardiovascular system, including positive inotropic, anti-arrhythmia and anti-oxidant activities; it also has anti-apoptotic activity, which may contribute to the improvement of clinical outcomes in treating myocarditis with pharmaceutics of Astragalus membranaceus.
||Bcl-2/Bax | NF-kB | Caspase | NO | NOS | Trk receptor|
|Am J Chin Med. 2010;38(3):517-27. |
|Protective effect of astragaloside on focal cerebral ischemia/reperfusion injury in rats.[Pubmed: 20503469 ]|
|This study was to observe the neurological protective effects of Astragalosides (AST) on focal cerebral ischemia-reperfusion (I/R) injury in rats and to explore its possible mechanism.
METHODS AND RESULTS:
Male SD rats received right middle cerebral artery occlusion for 120 min and AST (40 mg/kg) was orally administered. The rats were decapitated 1, 3, 7, and 14 days after reperfusion. The neurological deficit score, infarct volume and water content of brain were measured; the activity of superoxide dismutase (SOD), lactate dehydrogenase (LDH) and nitric oxide synthase (NOS), and the content of malondialdehyde (MDA), lactate (LD) and nitric oxide (NO) of brain tissue were detected too. The expression of inducible nitric synthase (iNOS), nerve growth factor (NGF) and tropomyosin receptor kinase A (TrkA) mRNA were measured by RT-PCR or real-time PCR. AST could significantly reduce the neurological deficit score; infract volume and water content, increase SOD and LDH activities, decrease NOS activity and MDA, LD and NO content. AST treatment could down-regulate expression of iNOS mRNA, while, NGF and TrkA mRNA were up-regulated.
Our data suggest that AST have the protective effects on focal cerebral ischemia in rats at the different reperfusion time points, the mechanism may be related to the antioxidation, regulated the expressions of iNOS, NGF and TrkA mRNA.
||The roots of Astragalus membranaceus (Fisch.) Bunge
||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: 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.
|Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2014 Jun;22(3):703-6. |
|Role of BCL-2, caspase-3 and NF-κB in astragaloside inducing apoptosis of human NB4 cells.[Pubmed: 24989280]|
|This study was purposed to investigate the apoptosis-inducing effect of Astragalosides on acute promyelocytic leukemia(APL) cell line NB4 and its mechanism. |
METHODS AND RESULTS:
NB4 cells were treated with different concentrations (200, 300, 400 µg /ml) of Astragalosides for 48 h. The cell proliferation was assayed by using CCK-8 method; the cell apoptosis was analyzed by flow cytometry with Annexin V-FITE/PI double staining. The mRNA expression of BCL-2 and the relative activity of BCL-2, NF-κB and caspase-3 were detected by RT-PCR and Western blot, respectively. The results showed that after treated with Astragalosides for 48 h, Astragalosides inhibited NB4 cell proliferation in concentration-dependent way, the apoptosis rate of NB4 cells gradually elevated from 4.69% to 40.85% with the increasing of Astragalosides concentration. Simultaneously, the mRNA expression of BCL-2 was down-regulated, Western blot analysis showed that the protein expression levels of BCL-2 and NF-κB decreased after Astragalosides treatment, while caspase-3 protein expression level increased.
It is concluded that the molecular mechanism of the Astragalosides-induced apoptosis in NB4 cells may be associated with down-regulation of the expression of BCL-2 and NF-κB, finally the relative activity of caspase-3 activated.
|Am J Chin Med. 2014;42(6):1357-70. |
|Astragaloside improves outcomes of traumatic brain injury in rats by reducing microglia activation.[Pubmed: 25384449]|
|Astragaloside (AST) is traditionally prescribed for the prevention and treatment of cerebrovascular diseases.
METHODS AND RESULTS:
We directly tested the therapeutic effects of Astragaloside in a rat model of traumatic brain injury (TBI). One hour after the onset of TBI rats were given Saline (1 ml/kg) or Astragaloside (20-80 mg/kg) via i.p. injection. Astragaloside causes the attenuation of TBI-induced cerebral contusion, neuronal apoptosis, and neurological motor dysfunction. TBI-induced microglial activation evidenced by the morphological transformation of microglia (or ameboid microglia) and the microglial overexpression of tumor necrosis factor-alpha was reduced by Astragaloside .
Our results indicate that Astragaloside may protect against brain contusion and neuronal apoptosis after TBI by attenuating microglia activation in male rats.