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3,6-Dihydroxy-1,7-dimethoxyxanthone
ChemFaces products have been cited in many studies from excellent and top scientific journals
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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 / Inquiry |
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More articles cited ChemFaces products.
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- Fitoterapia.2022, 157:105130.
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- Research Square2020, doi: 10.21203.
- Antioxidants.2022, 11(4), 67.
- Institute of Food Science & Technology2021, 56(11).
- J Nat Prod.2019, 82(4):1002-1008
- Food Sci Biotechnol.2021, 30(2):217-226.
- Journal of Physiology & Pathology in Korean Medicine.2018, 32(2): 106-112
- J Separation Science & Technology2016, 51:1579-1588
- 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 |
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Description: |
3,6-Dihydroxy-1,7-dimethoxyxanthone is a natural product from Hypericum ascyro. |
3,6-Dihydroxy-1,7-dimethoxyxanthone Description
Source: |
The aerial parts of Hypericum ascyro. |
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 |
3.4692 mL |
17.3461 mL |
34.6921 mL |
69.3842 mL |
86.7303 mL |
5 mM |
0.6938 mL |
3.4692 mL |
6.9384 mL |
13.8768 mL |
17.3461 mL |
10 mM |
0.3469 mL |
1.7346 mL |
3.4692 mL |
6.9384 mL |
8.673 mL |
50 mM |
0.0694 mL |
0.3469 mL |
0.6938 mL |
1.3877 mL |
1.7346 mL |
100 mM |
0.0347 mL |
0.1735 mL |
0.3469 mL |
0.6938 mL |
0.8673 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, 1999, 52(7):1371-1373. | Xanthones from Hypericum ascyron.[Reference: WebLink] | The isolation and identification of eight xanthones, together with friedelin, from the aerial parts of Hypericum ascyron are reported. One of these xanthones, 3,6-Dihydroxy-1,7-dimethoxyxanthone is a new compound and the other 5-chloro-1,6-dihydroxy-3-methoxy-8-methylxanthone is the first chloroxanthone isolated from higher plants. |
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