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Ebracteolatanolide A

CAS# 212563-72-9

Ebracteolatanolide A

Catalog No. BCN3773----Order now to get a substantial discount!

Product Name & Size Price Stock
Ebracteolatanolide A:5mg Please Inquire In Stock
Ebracteolatanolide A:10mg Please Inquire In Stock
Ebracteolatanolide A:20mg Please Inquire In Stock
Ebracteolatanolide A:50mg Please Inquire In Stock

Quality Control of Ebracteolatanolide A

Number of papers citing our products

Chemical structure

Ebracteolatanolide A

3D structure

Chemical Properties of Ebracteolatanolide A

Cas No. 212563-72-9 SDF Download SDF
PubChem ID 102004596 Appearance Cryst.
Formula C20H28O4 M.Wt 332.4
Type of Compound Diterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
SMILES CC1=C2C(C(C3C4(CCCC(C4CCC35C2O5)(C)C)C)O)OC1=O
Standard InChIKey LDVDGGIHTUCGMX-REKFSXRJSA-N
Standard InChI InChI=1S/C20H28O4/c1-10-12-14(23-17(10)22)13(21)15-19(4)8-5-7-18(2,3)11(19)6-9-20(15)16(12)24-20/h11,13-16,21H,5-9H2,1-4H3/t11-,13+,14+,15+,16-,19-,20+/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 Ebracteolatanolide A

The herbs of Euphorbia ebracteolata

Biological Activity of Ebracteolatanolide A

DescriptionStandard reference

Protocol of Ebracteolatanolide A

Structure Identification
Yao Xue Xue Bao. 1998;33(2):128-31.

Studies on diterpenoids from the roots of Euphorbia ebracteolata.[Pubmed: 11938948]


METHODS AND RESULTS:
Euphorbia ebractolata has been used as insecticide and tuberculocide. Four crystalline compounds were isolated from the root of this plant. They were characterized by their physico-chemical properties and spectral data as: 3-acety alpha-amyrin (I), Jolkinolide B (II), Ebracteolatanolide A (III) and ebracteolatanolide B (IV). I and II were isolated for the first time from E. ebracteolata Hayata.
CONCLUSIONS:
Ebracteolatanolide A and IV are new compounds.

Ebracteolatanolide A Dilution Calculator

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Ebracteolatanolide A Molarity Calculator

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Preparing Stock Solutions of Ebracteolatanolide A

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.0084 mL 15.0421 mL 30.0842 mL 60.1685 mL 75.2106 mL
5 mM 0.6017 mL 3.0084 mL 6.0168 mL 12.0337 mL 15.0421 mL
10 mM 0.3008 mL 1.5042 mL 3.0084 mL 6.0168 mL 7.5211 mL
50 mM 0.0602 mL 0.3008 mL 0.6017 mL 1.2034 mL 1.5042 mL
100 mM 0.0301 mL 0.1504 mL 0.3008 mL 0.6017 mL 0.7521 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 Ebracteolatanolide A

[Studies on diterpenoids from the roots of Euphorbia ebracteolata].[Pubmed:11938948]

Yao Xue Xue Bao. 1998;33(2):128-31.

Euphorbia ebractolata has been used as insecticide and tuberculocide. Four crystalline compounds were isolated from the root of this plant. They were characterized by their physico-chemical properties and spectral data as: 3-acety alpha-amyrin (I), Jolkinolide B (II), Ebracteolatanolide A (III) and ebracteolatanolide B (IV). I and II were isolated for the first time from E. ebracteolata Hayata. III and IV are new compounds.

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