ChemFaces is a professional high-purity natural products manufacturer.
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1. Reference standards
2. Pharmacological research
3. Inhibitors
9-Dehydroxyeurotinone
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 / Inquiry |
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(21):5087. Horticulturae2021, 7(1),5.Trop J Nat Prod Res.2019, 3(1):6-9Nutrients2020, 12(2):488HIV Med.2021, 22(8):690-704.Cancer Manag Res.2019, 11:483-500Life Sci.2018, 209:498-506Yakugaku Zasshi.2018, 138(4):571-579
Korean Journal of Pharmacognosy...2018...Cell Physiol Biochem....2017...Biotechnol Bioeng....2020...Molecules.2021, 26(23):7390. Phytother Res.2019, 33(4):1104-1113BMC Complement Altern Med....2019...Front Pharmacol.2020, 11:683.Clin Transl Oncol.2019, 10.1007
Molecules 2022, 27(3),1047.Front Immunol.2017, 8:1542Heliyon2022, 8(2):e08866.JAOCS2021, 98(7):779-794.Biochem Biophys Res Commun....2017...J Biochem Mol Toxicol....2020...Korean Journal of Pharmacognosy...2014...
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Our products had been exported to the following research institutions and universities, And still growing.
University of Stirling (United Kingdom)University of Liège (Belgium)Florida International University (USA)Universidad de Ciencias y Artes... (Mexico)
University of Wuerzburg (Germany)Monash University (Australia)Universiti Malaysia Pahang (Malaysia)VIT University (India)
The Vancouver Prostate Centre (... (Canada)Shanghai Institute of Biochemis... (China)University of Toronto (Canada)
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9-Dehydroxyeurotinone
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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 of Dentistry & Oral Health2019, 2641-1962BMC Microbiol.2019, 19(1):78J Pharmaceut Biomed2020, 182:113110Life Sci.2019, 216:259-270Sci Rep.2019, 9:19059The Journal of Agromedicine and Medical Sciences2018, 4(1)J Med Food.2021, 24(3):209-217.Phytochemistry.2021, 181:112539. J Am Soc Mass Spectrom.2021, 32(9):2451-2462.J Pharm Biomed Anal.2019, 172:268-277
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: |
Reference standards. |
9-Dehydroxyeurotinone Description
| Source: |
The endophyte of Suaeda glauca |
| 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 |
3.6731 mL |
18.3655 mL |
36.7309 mL |
73.4619 mL |
91.8274 mL |
| 5 mM |
0.7346 mL |
3.6731 mL |
7.3462 mL |
14.6924 mL |
18.3655 mL |
| 10 mM |
0.3673 mL |
1.8365 mL |
3.6731 mL |
7.3462 mL |
9.1827 mL |
| 50 mM |
0.0735 mL |
0.3673 mL |
0.7346 mL |
1.4692 mL |
1.8365 mL |
| 100 mM |
0.0367 mL |
0.1837 mL |
0.3673 mL |
0.7346 mL |
0.9183 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: |
| Helvetica Chimica Acta, 2012, 95(1):163-168. | | Alkaloid and Anthraquinone Derivatives Produced by the Marine-Derived Endophytic Fungus Eurotium rubrum.[Reference: WebLink] |
METHODS AND RESULTS:
Cultivation of the fungal strain Eurotium rubrum, an endophytic fungus that was isolated from the inner tissue of the semi-mangrove plant Hibiscus tiliaceus, resulted in the isolation of one new dioxopiperazine alkaloid, 12-demethyl-12-oxo-eurotechinulin B (1), and one new anthraquinone derivative, 9-Dehydroxyeurotinone (2), together with ten known compounds including variecolorin J (3), eurotechinulin B (4), variecolorin G (5), alkaloid E-7 (6), cryptoechinuline G (7), isoechinulin B (8), 7-isopentenylcryptoechinuline D (9), 2-O-methyl-9-Dehydroxyeurotinone (10), emodin (11), and emodic acid (12).
CONCLUSIONS:
The structures of the isolated compounds were determined by extensive analysis of their spectroscopic data as well as by comparison with literature reports.
Some of the purified compounds were evaluated for antibacterial, antifungal, and cytotoxic activities. |
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