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2. Pharmacological research
3. Inhibitors
3-O-Methylellagic acid 3'-O-alpha-rhamnopyranoside
Citing Use of our Products
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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 / $413 / 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.
Molecules.2020, 25(11):2599. Journal of Ginseng Research...2019...PLoS One.2018, 13(11):e0208055Int J Mol Sci.2021, 22(19):10405.J Nat Med.2021, doi: 10.1007.Appl. Sci.2021, 11(24),12080Pharmaceutics2022, 14(2),376.PLoS One.2021, 16(9):e0257243.
J Food Biochem.2020, 44(6):e13198. Nat Commun.2019, 10(1):5169Anat Rec2018, 24264Phytochem Anal.2016, 27(5):296-303Evid Based Complement Alternat Me...2017...Sci Rep.2017, 7:46299Toxins (Basel).2021, 13(9):593. Sci Rep.2017, 7:40345
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Our products had been exported to the following research institutions and universities, And still growing.
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National Cancer Center Research... (Japan)Max Rubner-Institut (MRI) (Germany)Instituto de Investigaciones Ag... (Chile)University of Bordeaux (France)
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3-O-Methylellagic acid 3'-O-alpha-rhamnopyranoside
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manager@chemfaces.com
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+86-27-84254680
Address:
1 Building, No. 83, CheCheng Rd., Wuhan Economic and Technological Development Zone, Wuhan, Hubei 430056, PRC
Viruses.2017, 9(10)J. of Agricultural Science2015, 1916-9760Int J Mol Sci.2019, 20(3):E651Korean J Dent Mater2020, 47(2):63-70.Int J Mol Sci.2021, 22(21):11836.Current Pharmaceutical Analysis2017, 13(5)Phytother Res.2016, 30(12):2020-2026Molecules.2019, 24(24),4583Cosmetics2021, 8(3),91.Korean Journal of Medicinal Crop Science2018, 26(5):382-390
Related Screening Libraries
| Size /Price /Stock |
10 mM * 100 uL in DMSO / Inquiry / In-stock
10 mM * 1 mL in DMSO / Inquiry / In-stock
|
Related Libraries |
Phenols Compound Library |
| Description: |
3-O-Methylellagic acid 3'-O-α-rhamnopyranoside has antioxidant and antibacterial activity. |
| In vitro: |
| Phytochemistry . 2001 Jun;57(4):587-591. | | Ellagic acid rhamnosides from the stem bark of Eucalyptus globulus[Pubmed: 11394863] | | Four ellagic acid rhamnosides were isolated from the stem bark of Eucalyptus globulus. Their structures have been established on the basis of the analysis of their 1H NMR, 13C NMR, HMBC, IR and MS spectral data. The HMBC data of these compounds were most useful for their structure determinations, with these bring determined to be 3-O-Methylellagic acid 3'-O-alpha-rhamnopyranoside, 3-O-methylellagic acid 3'-O-alpha-3''-O-acetylrhamnopyranoside, 3-O-methylellagic acid 3'-O-alpha-2''-O-acetylrhamnopyranoside, 3-O-methylellagic acid 3'-O-alpha-4''-O-acetylrhamnopyranoside, respectively. Their antioxidant activities were evaluated by measuring the inhibition of lipid peroxidation using rat liver microsomes, with IC50 values of 10.0-14.0 microg/ml. | | Nat Prod Res . 2014;28(4):230-238. | | Isolation, characterisation and antibacterial activity of new compounds from methanolic extract of seeds of Caesalpinia crista L. (Caesalpinaceae)[Pubmed: 23822804] | | Phytochemical study on the methanolic extract of Caesalpinia crista afforded two novel compounds, 2-hydroxytrideca-3,6-dienyl-pentanoate and octacosa-12,15-diene along with known compounds 3-O-methylellagic acid 3'O-α-rhamnopyranoside, β-sitosterol and sucrose. Compound 3-O-methylellagic acid 3'O-α-rhamnopyranoside is reported for the first time from the plant. Molecular structures, of isolated compounds, were elucidated by using the NMR spectroscopy in combination with IR and mass spectral data. All isolated compounds, extract and fractions were evaluated for in vitro antibacterial activity against various Gram-positive and Gram-negative bacterial strains and found to be significantly active against Staphylococcus aureus and methicillin-resistant S. aureus (minimum inhibitory concentration: 64-512 μg mL(- 1)). |
|
3-O-Methylellagic acid 3'-O-alpha-rhamnopyranoside Description
| Source: |
The peels of Punica granatum 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 |
2.1626 mL |
10.8131 mL |
21.6263 mL |
43.2526 mL |
54.0657 mL |
| 5 mM |
0.4325 mL |
2.1626 mL |
4.3253 mL |
8.6505 mL |
10.8131 mL |
| 10 mM |
0.2163 mL |
1.0813 mL |
2.1626 mL |
4.3253 mL |
5.4066 mL |
| 50 mM |
0.0433 mL |
0.2163 mL |
0.4325 mL |
0.8651 mL |
1.0813 mL |
| 100 mM |
0.0216 mL |
0.1081 mL |
0.2163 mL |
0.4325 mL |
0.5407 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.
| Structure Identification: |
| Phytochemistry . 2001 Jun;57(4):587-591. | | Ellagic acid rhamnosides from the stem bark of Eucalyptus globulus[Pubmed: 11394863] | | Four ellagic acid rhamnosides were isolated from the stem bark of Eucalyptus globulus. Their structures have been established on the basis of the analysis of their 1H NMR, 13C NMR, HMBC, IR and MS spectral data. The HMBC data of these compounds were most useful for their structure determinations, with these bring determined to be 3-O-Methylellagic acid 3'-O-alpha-rhamnopyranoside, 3-O-methylellagic acid 3'-O-alpha-3''-O-acetylrhamnopyranoside, 3-O-methylellagic acid 3'-O-alpha-2''-O-acetylrhamnopyranoside, 3-O-methylellagic acid 3'-O-alpha-4''-O-acetylrhamnopyranoside, respectively. Their antioxidant activities were evaluated by measuring the inhibition of lipid peroxidation using rat liver microsomes, with IC50 values of 10.0-14.0 microg/ml. | | Nat Prod Res . 2014;28(4):230-238. | | Isolation, characterisation and antibacterial activity of new compounds from methanolic extract of seeds of Caesalpinia crista L. (Caesalpinaceae)[Pubmed: 23822804] | | Phytochemical study on the methanolic extract of Caesalpinia crista afforded two novel compounds, 2-hydroxytrideca-3,6-dienyl-pentanoate and octacosa-12,15-diene along with known compounds 3-O-methylellagic acid 3'O-α-rhamnopyranoside, β-sitosterol and sucrose. Compound 3-O-methylellagic acid 3'O-α-rhamnopyranoside is reported for the first time from the plant. Molecular structures, of isolated compounds, were elucidated by using the NMR spectroscopy in combination with IR and mass spectral data. All isolated compounds, extract and fractions were evaluated for in vitro antibacterial activity against various Gram-positive and Gram-negative bacterial strains and found to be significantly active against Staphylococcus aureus and methicillin-resistant S. aureus (minimum inhibitory concentration: 64-512 μg mL(- 1)). |
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