Ecliptasaponin D

CAS# 206756-04-9

Ecliptasaponin D

2D Structure

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3D structure

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Ecliptasaponin D

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Chemical Properties of Ecliptasaponin D

Cas No. 206756-04-9 SDF Download SDF
PubChem ID 102004874 Appearance Powder
Formula C36H58O9 M.Wt 634.84
Type of Compound Triterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (4aR,5S,6aR,6aS,6bR,8aR,10S,12aR,14bS)-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid
SMILES CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)C(=O)O)C
Standard InChIKey WYDPEADEZMZKNM-USLJWFFESA-N
Standard InChI InChI=1S/C36H58O9/c1-31(2)14-15-36(30(42)43)20(16-31)19-8-9-23-33(5)12-11-25(45-29-28(41)27(40)26(39)21(18-37)44-29)32(3,4)22(33)10-13-34(23,6)35(19,7)17-24(36)38/h8,20-29,37-41H,9-18H2,1-7H3,(H,42,43)/t20-,21+,22-,23+,24-,25-,26+,27-,28+,29-,33-,34+,35+,36+/m0/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 Ecliptasaponin D

The herbs of Eclipta prostrata

Protocol of Ecliptasaponin D

Structure Identification
Yao xue xue bao = Acta pharmaceutica Sinica, 1997, 32(8):633-634.

Isolation and identification of ecliptasaponin D from Eclipta alba (L.) Hassk.[Reference: WebLink]


METHODS AND RESULTS:
A new triterpenoid glucoside Ecliptasaponin D was isolated from Eclipta alba (L.) Hassk. Its structure was deduced as 3 beta, 16 beta-dihydroxy olean-12-ene-28-oic acid-3 beta-O-beta-D-glucopyranoside, based on spectral analysis and chemical evidences as well as results of hydrolysis.

Ecliptasaponin D Dilution Calculator

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Preparing Stock Solutions of Ecliptasaponin D

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.5752 mL 7.876 mL 15.752 mL 31.504 mL 39.38 mL
5 mM 0.315 mL 1.5752 mL 3.1504 mL 6.3008 mL 7.876 mL
10 mM 0.1575 mL 0.7876 mL 1.5752 mL 3.1504 mL 3.938 mL
50 mM 0.0315 mL 0.1575 mL 0.315 mL 0.6301 mL 0.7876 mL
100 mM 0.0158 mL 0.0788 mL 0.1575 mL 0.315 mL 0.3938 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 Ecliptasaponin D

[Isolation and identification of ecliptasaponin D from Eclipta alba (L.) Hassk].[Pubmed:11596317]

Yao Xue Xue Bao. 1997 Aug;32(8):633-4.

A new triterpenoid glucoside Ecliptasaponin D was isolated from Eclipta alba (L.) Hassk. Its structure was deduced as 3 beta, 16 beta-dihydroxy olean-12-ene-28-oic acid-3 beta-O-beta-D-glucopyranoside, based on spectral analysis and chemical evidences as well as results of hydrolysis.

Description

Ecliptasaponin D is a triterpenoid glucoside isolated from Eclipta alba (L.) Hassk which is the aerial part of Eclipta prostrate. Eclipta prostrate is considered as a nourishing herbal medicine with pleiotropic effects, including anti-inflammatory, hepatoprotective, antioxidant and immunomodulatory[1,2].

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