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- 1. Reference standards
- 2. Pharmacological research
- 3. Inhibitors
5,8,9,10,14-Pentaacetoxy-3-benzoyloxy-15-hydroxypepluane
ChemFaces products have been cited in many studies from excellent and top scientific journals
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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 / 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.
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Our products had been exported to the following research institutions and universities, And still growing.
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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 |
|
| Description: |
Reference standards. |
5,8,9,10,14-Pentaacetoxy-3-benzoyloxy-15-hydroxypepluane Description
| Source: |
The herbs of Euphorbia peplus |
| 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 |
1.4269 mL |
7.1347 mL |
14.2694 mL |
28.5388 mL |
35.6735 mL |
| 5 mM |
0.2854 mL |
1.4269 mL |
2.8539 mL |
5.7078 mL |
7.1347 mL |
| 10 mM |
0.1427 mL |
0.7135 mL |
1.4269 mL |
2.8539 mL |
3.5674 mL |
| 50 mM |
0.0285 mL |
0.1427 mL |
0.2854 mL |
0.5708 mL |
0.7135 mL |
| 100 mM |
0.0143 mL |
0.0713 mL |
0.1427 mL |
0.2854 mL |
0.3567 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: |
| Chinese Journal of Natural Medicines, 2010, 8(2):81-83. | | A New Jatrophane Diterpenoid from Euphorbia peplus.[Reference: WebLink] | To study the chemical constituents of Euphorbia peplus.
METHODS AND RESULTS:
Compounds 1–3 were isolated and purified by silica gel column chromatography, MCI and Sephadex LH-20. Their structures were mainly elucidated by spectroscopic analysis and physicochemical characteristics. Three compounds were identified as euphopeplin A (1), 2α, 5α, 7β, 8α, 9α, 14β-hexaacetoxy-3β-benzoyloxy-15-hydroxyjatropha-6 (17), 11E-diene (2) and 5α, 8α, 9β, 10β, 14α-pentaacetoxy-3β-benzoy-loxy-15-hydroxypepluane (5,8,9,10,14-Pentaacetoxy-3-benzoyloxy-15-hydroxypepluane,3).
CONCLUSIONS:
A new jatrophane diterpenoid, euphopeplin A (1) was isolated from Euphorbia peplus. |
|
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