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Cixiophiopogon A

CAS# 288143-27-1

Cixiophiopogon A

Catalog No. BCN2778----Order now to get a substantial discount!

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Cixiophiopogon A: 5mg $98 In Stock
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Quality Control of Cixiophiopogon A

Number of papers citing our products

Chemical structure

Cixiophiopogon A

3D structure

Chemical Properties of Cixiophiopogon A

Cas No. 288143-27-1 SDF Download SDF
PubChem ID 102004869 Appearance Powder
Formula C44H70O18 M.Wt 887.02
Type of Compound Steroids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
SMILES CC1CCC2(C(C3(C(O2)CC4(C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)O)O)C)OC1
Standard InChIKey XEMVQWDHRXAQNR-YVEJFGEMSA-N
Standard InChI InChI=1S/C44H70O18/c1-19-8-13-43(56-17-19)21(3)44(54)28(62-43)15-42(53)25-7-6-22-14-23(9-11-40(22,4)24(25)10-12-41(42,44)5)58-39-36(61-38-34(52)32(50)29(47)20(2)57-38)35(31(49)27(16-45)59-39)60-37-33(51)30(48)26(46)18-55-37/h6,19-21,23-39,45-54H,7-18H2,1-5H3/t19-,20+,21-,23+,24+,25-,26-,27-,28+,29+,30+,31-,32-,33-,34-,35+,36-,37+,38+,39-,40+,41+,42-,43-,44-/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 Cixiophiopogon A

The roots of Ophiopogon japonicus

Biological Activity of Cixiophiopogon A

DescriptionCixiophiopogon A is a natural product from Ophiopogon japonicus.

Protocol of Cixiophiopogon A

Structure Identification
Natural Product Research: Formerly Natural Product Letters Volume 25, Issue 1, 2011

A new steroidal glycoside from the Ophiopogon japonicus Ker-Gawler (Liliaceae)[Reference: WebLink]


METHODS AND RESULTS:
A new steroidal glycoside (1), (25R)-14α, 17α-hydroxyspirost-5-en-3β-yl 3-O-α-L-rhamnpyranosyl-(1 → 2)-β-D-glucopyranosyl-(1 → 3)-β-D-glucopyranoside, together with three known steroidal glycosides, (25R)-3β-hydroxyspirost-5-en-1β-yl-3-O-α-L-rhamnopyranosyl-(1 → 2)-O-β-D-xylopyranosyl-(1 → 3)-α-L-arabinopyranoside (2), Cixi-ophiopogon B (3) and Cixiophiopogon A (4), were obtained from the tuberous roots of Ophiopogon japonicus (Liliaceae). Compound 2 was isolated from the Ophiopogon genus for the first time.
CONCLUSIONS:
Their structures were identified on the basis of extensive mass and nuclear magnetic resonance spectroscopic analysis.

Cixiophiopogon A Dilution Calculator

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Cixiophiopogon A Molarity Calculator

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Preparing Stock Solutions of Cixiophiopogon A

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.1274 mL 5.6369 mL 11.2737 mL 22.5474 mL 28.1843 mL
5 mM 0.2255 mL 1.1274 mL 2.2547 mL 4.5095 mL 5.6369 mL
10 mM 0.1127 mL 0.5637 mL 1.1274 mL 2.2547 mL 2.8184 mL
50 mM 0.0225 mL 0.1127 mL 0.2255 mL 0.4509 mL 0.5637 mL
100 mM 0.0113 mL 0.0564 mL 0.1127 mL 0.2255 mL 0.2818 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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Description

Cixiophiopogon A, a steroidal glycoside, obtained from the tuberous roots of Ophiopogon japonicus (Liliaceae).

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