Vibralactone L

CAS# 1623786-67-3

Vibralactone L

Catalog No. BCN6914----Order now to get a substantial discount!

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Vibralactone L: 5mg Please Inquire In Stock
Vibralactone L: 10mg Please Inquire In Stock
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Quality Control of Vibralactone L

Number of papers citing our products

Chemical structure

Vibralactone L

3D structure

Chemical Properties of Vibralactone L

Cas No. 1623786-67-3 SDF Download SDF
PubChem ID 131849277 Appearance Oil
Formula C14H20O4 M.Wt 252.31
Type of Compound Sesquiterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name ethyl 5-methyl-2-[(5-oxo-2H-furan-3-yl)methyl]hex-4-enoate
SMILES CCOC(=O)C(CC=C(C)C)CC1=CC(=O)OC1
Standard InChIKey IUKVKDVSDJSIKQ-UHFFFAOYSA-N
Standard InChI InChI=1S/C14H20O4/c1-4-17-14(16)12(6-5-10(2)3)7-11-8-13(15)18-9-11/h5,8,12H,4,6-7,9H2,1-3H3
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Source of Vibralactone L

The cultures of the Basidiomycete Boreostereum vibrans.

Biological Activity of Vibralactone L

DescriptionVibralactone L is a natural product from Basidiomycete Boreostereum vibrans.

Protocol of Vibralactone L

Structure Identification
J Asian Nat Prod Res. 2014;16(5):447-52

Three new vibralactone-related compounds from cultures of Basidiomycete Boreostereum vibrans.[Pubmed: 24684503 ]


METHODS AND RESULTS:
Three new compounds, named as vibralactones K-M (1-3), together with vibralactone (4) have been isolated from cultures of the Basidiomycete Boreostereum vibrans. Their structures were determined on the basis of spectroscopic evidences (1D and 2D NMR, HRMS, UV, and IR data), chemical methods and literature data.
CONCLUSIONS:
None of the compounds was cytotoxic against five human cancer cell lines and showed inhibitory activity on the pancreatic lipase.

Vibralactone L Dilution Calculator

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Vibralactone L Molarity Calculator

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Preparing Stock Solutions of Vibralactone L

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.9634 mL 19.8169 mL 39.6338 mL 79.2676 mL 99.0845 mL
5 mM 0.7927 mL 3.9634 mL 7.9268 mL 15.8535 mL 19.8169 mL
10 mM 0.3963 mL 1.9817 mL 3.9634 mL 7.9268 mL 9.9084 mL
50 mM 0.0793 mL 0.3963 mL 0.7927 mL 1.5854 mL 1.9817 mL
100 mM 0.0396 mL 0.1982 mL 0.3963 mL 0.7927 mL 0.9908 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

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References on Vibralactone L

Three new vibralactone-related compounds from cultures of Basidiomycete Boreostereum vibrans.[Pubmed:24684503]

J Asian Nat Prod Res. 2014;16(5):447-52.

Three new compounds, named as vibralactones K-M (1-3), together with vibralactone (4) have been isolated from cultures of the Basidiomycete Boreostereum vibrans. Their structures were determined on the basis of spectroscopic evidences (1D and 2D NMR, HRMS, UV, and IR data), chemical methods and literature data. None of the compounds was cytotoxic against five human cancer cell lines and showed inhibitory activity on the pancreatic lipase.

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