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Dodovislactone B

CAS# 1616683-55-6

Dodovislactone B

Catalog No. BCN7398----Order now to get a substantial discount!

Product Name & Size Price Stock
Dodovislactone B:5mg Please Inquire In Stock
Dodovislactone B:10mg Please Inquire In Stock
Dodovislactone B:20mg Please Inquire In Stock
Dodovislactone B:50mg Please Inquire In Stock

Quality Control of Dodovislactone B

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Chemical structure

Dodovislactone B

3D structure

Chemical Properties of Dodovislactone B

Cas No. 1616683-55-6 SDF Download SDF
PubChem ID 131849249 Appearance Powder
Formula C21H30O5 M.Wt 362.46
Type of Compound Diterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (4aR,5S,6R,8aR)-5-[2-(2-methoxy-5-oxo-2H-furan-3-yl)ethyl]-5,6,8a-trimethyl-3,4,4a,6,7,8-hexahydronaphthalene-1-carboxylic acid
SMILES CC1CCC2(C(C1(C)CCC3=CC(=O)OC3OC)CCC=C2C(=O)O)C
Standard InChIKey FYZIMPKKBJIMEN-RFZNXHICSA-N
Standard InChI InChI=1S/C21H30O5/c1-13-8-10-21(3)15(18(23)24)6-5-7-16(21)20(13,2)11-9-14-12-17(22)26-19(14)25-4/h6,12-13,16,19H,5,7-11H2,1-4H3,(H,23,24)/t13-,16-,19?,20+,21+/m1/s1
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 Dodovislactone B

The aerial parts of Dodonaea viscosa.

Biological Activity of Dodovislactone B

DescriptionDodovislactone B is a natural product from Dodonaea viscosa.

Protocol of Dodovislactone B

Structure Identification
Natural Products & Bioprospecting, 2013, 3(5):250-255.

Isoprenylated flavonoids and clerodane diterpenoids from Dodonaea viscosa.[Reference: WebLink]

Phytochemical investigation of the aerial parts of Dodonaea viscosa led to the isolation of six new compounds including four isoprenylated flavonoids, dodovisones A-D (1–4), and two clerodane diterpenoids, dodovislactone A and Dodovislactone B (5 and 6). Their structures were established by extensive spectroscopic analysis.

Dodovislactone B Dilution Calculator

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Dodovislactone B Molarity Calculator

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Preparing Stock Solutions of Dodovislactone B

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.7589 mL 13.7946 mL 27.5893 mL 55.1785 mL 68.9731 mL
5 mM 0.5518 mL 2.7589 mL 5.5179 mL 11.0357 mL 13.7946 mL
10 mM 0.2759 mL 1.3795 mL 2.7589 mL 5.5179 mL 6.8973 mL
50 mM 0.0552 mL 0.2759 mL 0.5518 mL 1.1036 mL 1.3795 mL
100 mM 0.0276 mL 0.1379 mL 0.2759 mL 0.5518 mL 0.6897 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 Dodovislactone B

Isoprenylated flavonoids and clerodane diterpenoids from Dodonaea viscosa.

Natural Products & Bioprospecting, 2013, 3(5):250-255.

Phytochemical investigation of the aerial parts of Dodonaea viscosa led to the isolation of six new compounds including four isoprenylated flavonoids, dodovisones A-D (1–4), and two clerodane diterpenoids, dodovislactone A and Dodovislactone B (5 and 6). Their structures were established by extensive spectroscopic analysis.

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