ChemFaces is a professional high-purity natural products manufacturer.
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2. Pharmacological research
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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 / $368 / 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.
Life (Basel).2021, 11(7):616. Molecules.2020, 25(21):5091.United States Patent Application...2020...Pharmaceutics.2021, 13(2):187. Journal of Apiculture...2019...Antioxidants (Basel).2020, 9(6):526.Biochem Biophys Res Commun....2017...J Med Food.2019, 22(10):1067-1077
Nutrients.2020, 12(11):3448. J Ethnopharmacol.2017, 198:205-213Gene.2022, 815:146178.Heliyon2020, 6(6):e04337.Integr Med Res.2017, 6(4):395-403Biomed Pharmacother.2021, 144:112300.BMC Complement Altern Med....2019...J Nat Prod.2018, 81(4):966-975
Int J Pharmacol2020, 16:1-9Appl Biol Chem2019, 62:46International J of Green Pharmacy...2019...Phytother Res.2018, 32(12):2551-2559Am J Chin Med.2015, 30:1-22Biomedicines.2021, 9(8):996.Phytochemistry Letters2021, 43:80-87.
Our products had been exported to the following research institutions and universities, And still growing.
University of Stirling (United Kingdom)University of Beira Interior (Portugal)University of Toulouse (France)University of Toronto (Canada)
VIT University (India)University of Ioannina (Greece)Universidad de La Salle (Mexico)Sanford Burnham Prebys Medical ... (USA)
Instituto de Investigaciones Ag... (Chile)University of Wuerzburg (Germany)Lodz University of Technology (Poland)
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1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
Journal of Apiculture2019, 34(2):131-136Asian Pac J Cancer Prev.2021, 22(S1):97-106.J Am Soc Mass Spectrom.2021, 32(9):2451-2462.Molecules.2018, 23(12):E3103J Ethnopharmacol.2021, 267:113615.Int J Mol Sci.2021, 22(19):10405.Enzyme and Microbial Technology2022, 110002.Front Pharmacol.2021, 12:635510.Front Pharmacol.2018, 9:756Molecules.2019, 25(1):E103
Related Screening Libraries
|Size /Price /Stock
||10 mM * 100 uL in DMSO / Inquiry / In-stock |
10 mM * 1 mL in DMSO / Inquiry / In-stock
||Phenols Compound Library
|| Reference standards.|
|J Agric Food Chem. 2007 Sep 19;55(19):7753-7. |
|Oligomers of resveratrol and ferulic acid prepared by peroxidase-catalyzed oxidation and their protective effects on cardiac injury.[Pubmed: 17696480 ]|
METHODS AND RESULTS:
Peroxidase extracted from Momordica charantia was used for the oligomerization of trans-resveratrol and ferulic acid on a preparative scale.
One new heterocoupling oligomer, trans-3 E-3-[(4-hydroxy-3-methoxyphenyl)methylene]-4-(3,5-dihydroxyphenyl)-5-(4-hydroxyphenyl)tetrahydro-2-franone (6), and six resveratrol dimers, Leachianol G (1), restrytisol B (2), parthenostilbenins A (3) and B (5), 7- O-acetylated Leachianol G (4), and resveratrol trans-dehydrodimer (8), and one known ferulic acid dehydrodimer, (3alpha,3aalpha,6alpha,6aalpha)tetrahydro-3,6-bis(4-hydroxy-3-methoxyphenyl)-1 H,4 H-furo[3,4-c]furan-1,4-dione (7) were obtained.
Bioactive experiments showed that compounds 6- 8 have strong free radical scavenging effects and also have protective effects on doxorubicin-induced cardiac cell injury when tested in vitro.
Leachianol G Description
||The roots of Ampelopsis brevipedunculata var. hancei
||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: 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.
|Molecules. 2017 Mar 16;22(3). pii: E474. |
|Anti-Cancer Activity of Resveratrol and Derivatives Produced by Grapevine Cell Suspensions in a 14 L Stirred Bioreactor.[Pubmed: 28300789 ]|
|In the present study, resveratrol and various oligomeric derivatives were obtained from a 14 L bioreactor culture of elicited grapevine cell suspensions (Vitis labrusca L.).
METHODS AND RESULTS:
The crude ethyl acetate stilbene extract obtained from the culture medium was fractionated by centrifugal partition chromatography (CPC) using a gradient elution method and the major stilbenes contained in the fractions were subsequently identified by using a 13C-NMR-based dereplication procedure and further 2D NMR analyses including HSQC, HMBC, and COSY. Beside δ-viniferin (2), leachianol F (4) and Leachianol G (4'), four stilbenes (resveratrol (1), ε-viniferin (5), pallidol (3) and a newly characterized dimer (6)) were recovered as pure compounds in sufficient amounts to allow assessment of their biological activity on the cell growth of three different cell lines, including two human skin malignant melanoma cancer cell lines (HT-144 and SKMEL-28) and a healthy human dermal fibroblast HDF line. Among the dimers obtained in this study, the newly characterized resveratrol dimer (6) has never been described in nature and its biological potential was evaluated here for the first time.
ε-viniferin as well as dimer (6) showed IC50 values on the three tested cell lines lower than the ones exerted by resveratrol and pallidol.
However, activities of the first two compounds were significantly decreased in the presence of fetal bovine serum although that of resveratrol and pallidol was not. The differential tumor activity exerted by resveratrol on healthy and cancer lines was also discussed.