ChemFaces is a professional high-purity natural products manufacturer.
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1. Reference standards
2. Pharmacological research
3. Inhibitors
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* 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 / $331.2 / 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.
J. of Med. Plant Research.2013, 90-151Antiviral Res.2013, 98(3):386-93Industrial Food Engineering...2015...Inflammation.2015, 38(4):1502-16Chemistry of Plant Materials....2016...Int J Mol Med.2016, 37(2):501-8Mol Immunol. 2016, 78:121-132Oncotarget.2017, 8(53):90925-90947
Analytical Methods2018, 10(27)Molecules.2018, 23(11):E2837J Pharm Biomed Anal.2019, 164:119-127Int J Mol Sci.2019, 20(16):E4015Molecules.2019, 24(10):E1930Molecules.2019, 25(1):E103Food Chem.2019, 276:768-775New Journal of Chemistry...2019...
Sci Rep.2019, 9(1):18080Sci Rep.2019, 9:19059J Cell Mol Med....2020...Eur Rev Med Pharmacol Sci....2020...Analytical Letters.2020, doi 10.1008Clin Exp Pharmacol Physiol....2020...Separations2021, 8(1), 1.
More...
Our products had been exported to the following research institutions and universities, And still growing.
Sapienza University of Rome (Italy)Universidade da Beira Interior (Germany)Melbourne University (Australia)Kyushu University (Japan)
Subang Jaya Medical Centre (Malaysia)Universit?t Basel (Switzerland)Periyar University (India)Indian Institute of Science (India)
University of Vienna (Austria)Copenhagen University (Denmark)Srinakharinwirot University (Thailand)
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Vicenin -1
Inquire / Order:
manager@chemfaces.com
Technical Inquiries:
service@chemfaces.com
Tel:
+86-27-84237783
Fax:
+86-27-84254680
Address:
1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
J Mol Histol.2019, 50(4):343-354Sci Rep.2019, 9:19059Phytomedicine.2017, 24:77-86Asian J Beauty Cosmetol2016, 14(3):249-257Arch Biochem Biophys.2018, 644:93-99Sci Rep.2018, 8:15059Int J Mol Sci.2020, 21(22):8816. Korean Herb. Med. Inf.2020, 8(2):243-254.International. J. of Food Properties 2017, 20:S131-S140Cell Physiol Biochem.2017, 43(4):1425-1435
Related Screening Libraries
| Description: |
Vicenin-1 possesses potent anti-inflammatory and anti-oxidant activity. |
| Targets: |
Aldose reductase |
| In vitro: |
| Journal of the Korean Society for Applied Biological Chemistry, 2015, 58(3):365-371. | | Plant-derived molecules from Saussurea grandifolia as inhibitors of aldose reductase.[Reference: WebLink] | Saussurea grandifolia was tested for aldose reductase (AR) inhibition as part of a search for potentially therapeutic natural compounds.
METHODS AND RESULTS:
Stepwise polarity fractions were tested for in vitro inhibition of rat lens AR. Of these, the ethyl acetate (EtOAc) and n-butanol (n-BuOH) fractions exhibited AR inhibitory activities. A chromatographic separation of the active EtOAc and n-BuOH fractions led to the isolation of nine compounds, which were known and identified as vitexin (1), genkwanin-5-O-glucoside (2), vitexin 2″-p-hydroxybenzoate (3), kaempferol-3-O-rutinoside (4), isovitexin (5), quercitrin (6), isoquercitrin (7), 1,5-di-O-caffeoylquinic acid (8), and Vicenin -1 (9). Among these compounds, compounds 6, 7, and 8 showed very strong inhibitory activities against AR (IC50’s = 0.34, 0.32, and 0.08 μM, respectively).
CONCLUSIONS:
The results suggest that S. grandifolia is clearly a potential source for therapeutic agent that might be useful for the treatment of diabetic complications. |
|
Vicenin -1 Description
| Source: |
The herbs of Vitex negundo L. |
| Solvent: |
DMSO, Pyridine, Methanol, Ethanol, etc. |
| Storage: |
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: service@chemfaces.com
|
| After receiving: |
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)
|
1 mg |
5 mg |
10 mg |
20 mg |
25 mg |
| 1 mM |
1.7715 mL |
8.8574 mL |
17.7148 mL |
35.4296 mL |
44.287 mL |
| 5 mM |
0.3543 mL |
1.7715 mL |
3.543 mL |
7.0859 mL |
8.8574 mL |
| 10 mM |
0.1771 mL |
0.8857 mL |
1.7715 mL |
3.543 mL |
4.4287 mL |
| 50 mM |
0.0354 mL |
0.1771 mL |
0.3543 mL |
0.7086 mL |
0.8857 mL |
| 100 mM |
0.0177 mL |
0.0886 mL |
0.1771 mL |
0.3543 mL |
0.4429 mL |
* 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.
| Animal Research: |
| Regulatory Toxicology and Pharmacology, 2016:S0273230016303026. | | Acute and repeated doses (28 days) oral toxicity study of Vicenin-1, a flavonoid glycoside isolated from fenugreek seeds in laboratory mice.[Reference: WebLink] | Vicenin -1 (fenugreek glycoside) has been proven to possess potent anti-inflammatory and anti-oxidant activity. The objective of the present investigation was to determine in-vivo acute and subacute (28-days repeated dose) oral toxicity of Vicenin -1 isolated from fenugreek seed.
METHODS AND RESULTS:
Vicenin-1 (93%) was isolated from a hydroalcoholic extract of fenugreek seed and characterized using HPLC, TLC, 1H NMR and 13C NMR. Acute oral toxicity (AOT) and subacute toxicity studies of Vicenin -1 were carried out according to OECD 425 (up-and-down procedure) and OCED 407 guidelines in Swiss albino mice. In AOT, Vicenin -1showed 10% mortality when administered at a dose of 5000 mg/kg. However, when vicenin-1 was administered for at doses of 37.5, 75, or 150 mg/kg 28-days it did not show any mortality at the administered doses. Vicenin -1 (75 mg/kg) did not show observational, behavioral, biochemical or histopathological toxic effects. There were minor alterations in body weight, hematology, and histopathology of mice administered with Vicenin -1
(150 mg/kg), but these changes were within normal laboratory ranges. The highest concentration of Venicin-1 was found in liver (3.46%) followed by lung (0.65%).
CONCLUSIONS:
In conclusion, Vicenin -1 showed median lethal dose (LD50) of 4837.5 mg/kg with no-observed-adverse-effect levels (NOAEL) at 75 mg/kg and lowest adverse effect levels (LOAEL) at 150 mg/kg for both sexes of mice during AOT and sub-acute toxicity study, respectively. |
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