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(1,5E,11E)-tridecatriene-7,9-diyne-3,4-diacetate
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 / $175.7 / In-stock |
Other Packaging |
*Packaging according to customer requirements(100uL/well, 200uL/well and more), and Container use Storage Tube With Screw Cap |
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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. |
(1,5E,11E)-tridecatriene-7,9-diyne-3,4-diacetate Description
| Source: |
The roots of Atractylodes chinensis |
| 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 |
3.33 mL |
16.65 mL |
33.3 mL |
66.6001 mL |
83.2501 mL |
| 5 mM |
0.666 mL |
3.33 mL |
6.66 mL |
13.32 mL |
16.65 mL |
| 10 mM |
0.333 mL |
1.665 mL |
3.33 mL |
6.66 mL |
8.325 mL |
| 50 mM |
0.0666 mL |
0.333 mL |
0.666 mL |
1.332 mL |
1.665 mL |
| 100 mM |
0.0333 mL |
0.1665 mL |
0.333 mL |
0.666 mL |
0.8325 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 (Oxford), 1997, 46(6):1023-1028. | | Diacetoxy-substituted polyacetylenes from Atractylodes lancea.[Reference: WebLink] |
METHODS AND RESULTS:
Six new polyacetylenes have been isolated from the rhizomes of Atractylodes lancea. Besides 1-(2-furyl)-(7E)-nonene-3,5-diyne-1,2-diacetate, a new natural compound, two further vicinal diacetoxyalkenynes were postulated as erythro- and threo-forms of
(1,5E,11E)-tridecatriene-7,9-diyne-3,4-diacetate in comparison with similar structures in the literature. Three other constituents turned out to be (3E,5E,11E)-tridecatriene-7,9-diyne-1,2-diacetate together with its (3Z)- and (5Z)-isomers.
CONCLUSIONS:
All structures were established by UV, EI-mass spectrometry, 1D and 2D NMR experiments. |
|
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