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3. Inhibitors
7-Methoxyneochamaejasmine A
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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 / $498.0 / 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.
Pharmacogn Mag.2015, 11:S585-91Mol Immunol. 2016, 78:121-132Plant Cell Tiss Org2017, 479-486Nat Prod Commun.2018, 10.1177ACS Nano.2018, 12(4):3385-3396Asian Journal of Chemistry...2018...J Sep Sci.2018, 41(9):1938-1946The Japan Society for Analytical ...2018...
Molecules.2019, 24(4):E744Molecules.2019, 24(7):E1290Toxicol Res.2019, 35(4):371-387New Journal of Chemistry...2019...J Agric Food Chem....2019...Food Sci Nutr.2019, 8(1):246-256Planta Med.2019, 85(4):347-355Drug Chem Toxicol.2020, 1-14.
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7-Methoxyneochamaejasmine A
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J of the Korean Society of Cosmetics and Cosmetology2019, 225-231Food Chem.2019, 274:345-350PLoS One.2017, 12(3):e0173585J. Soc. Cosmet. Sci. Korea2016, 163-171J Nat Med.2017, 71(2):380-388J Agric Food Chem.2019, 67(27):7748-7754Integr Med Res.2017, 6(4):395-403FASEB J.2019, 33(2):2026-2036Pharmaceutics.2020, 12(9):882. Nutrients.2020, 12(5):1242.
Related Screening Libraries
| Description: |
7-Methoxyneochamaejasmine A has a strong inhibitory effect on Festuca rubra L. and Medicago sativa seedlings. |
| In vitro: |
| Plant Growth Regulation, 2015 , 77 (3) :335-342. | | Potential allelochemicals in root zone soils of Stellera chamaejasme L. and variations at different geographical growing sites[Reference: WebLink] | Populations of Stellera chamaejasme L. have been increasing constantly in recent years in some areas of the grassland in north China but why this toxic weed has become highly competitive is not clear. In order to determine if any potential allelochemicals are released into the soil environment by S. chamaejasme, we investigated the chemical composition of a water-washed solution of the living roots with rhizosphere soil.
METHODS AND RESULTS:
This led to the isolation and identification of seven compounds: umbelliferone (1), daphnoretin (2), chamaechromone (3), 7-Methoxyneochamaejasmine A (4), mesoneochamaejasmin A (5), neochamaejasmin B (6), dihydrodaphnodorin B (7). All are secondary metabolites of S. chamaejasme. Bioassay showed that 1, 5 and 6 had a strong inhibitory effect on Festuca rubra L. and Medicago sativa seedlings. These compounds were quantified by high performance liquid chromatography in 25 root zone soil samples of S. chamaejasme collected at altitudes between 165 and 4741 m from the northeast to the Tibetan Plateau of China. All samples contained at least one of the phytotoxic compounds. Their content did not correlate with the altitude of the growing site. However, the level of chamaechromone negatively correlated with the soil pH.
CONCLUSIONS:
Principle components analysis indicated that the flavonoids might come from the same source. These potential allelochemicals from root release into the soil might play an important role in the highly competitive nature and broad ecological adaptability of S. chamaejasme in the wild. |
|
7-Methoxyneochamaejasmine A Description
| Source: |
The roots of Stellera chamaejasme Linn. |
| Solvent: |
Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, 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 |
1.7969 mL |
8.9847 mL |
17.9695 mL |
35.9389 mL |
44.9236 mL |
| 5 mM |
0.3594 mL |
1.7969 mL |
3.5939 mL |
7.1878 mL |
8.9847 mL |
| 10 mM |
0.1797 mL |
0.8985 mL |
1.7969 mL |
3.5939 mL |
4.4924 mL |
| 50 mM |
0.0359 mL |
0.1797 mL |
0.3594 mL |
0.7188 mL |
0.8985 mL |
| 100 mM |
0.018 mL |
0.0898 mL |
0.1797 mL |
0.3594 mL |
0.4492 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: |
| J Asian Nat Prod Res. 2002 Dec;4(4):259-63. | | Chemical constituents of Stellera chamaejasme L.[Pubmed: 12450253] | A new biflavanone, 7-Methoxyneochamaejasmine A, and a new chromone derivative, isomohsenone, were isolated from the roots of Stellera chamaejasme L.
METHODS AND RESULTS:
The structures of two compounds were determined by means of ESI-MS, 1H NMR and 13C NMR, especially 2D NMR spectral analyses. |
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