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Bis-5,5-nortrachelogenin

CAS# 870480-56-1

Bis-5,5-nortrachelogenin

Catalog No. BCN6516----Order now to get a substantial discount!

Product Name & Size Price Stock
Bis-5,5-nortrachelogenin:5mg Please Inquire In Stock
Bis-5,5-nortrachelogenin:10mg Please Inquire In Stock
Bis-5,5-nortrachelogenin:20mg Please Inquire In Stock
Bis-5,5-nortrachelogenin:50mg Please Inquire In Stock

Quality Control of Bis-5,5-nortrachelogenin

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Chemical structure

Bis-5,5-nortrachelogenin

3D structure

Chemical Properties of Bis-5,5-nortrachelogenin

Cas No. 870480-56-1 SDF Download SDF
PubChem ID 125115457 Appearance Powder
Formula C40H42O14 M.Wt 746.8
Type of Compound Lignans Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (3S,4S)-3-hydroxy-4-[[4-hydroxy-3-[2-hydroxy-5-[[(3S,4S)-4-hydroxy-4-[(4-hydroxy-3-methoxyphenyl)methyl]-5-oxooxolan-3-yl]methyl]-3-methoxyphenyl]-5-methoxyphenyl]methyl]-3-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one
SMILES COC1=C(C=CC(=C1)CC2(C(COC2=O)CC3=CC(=C(C(=C3)C4=CC(=CC(=C4O)OC)CC5COC(=O)C5(CC6=CC(=C(C=C6)O)OC)O)O)OC)O)O
Standard InChIKey UFFFFORCHIKZSY-YSECKRNDSA-N
Standard InChI InChI=1S/C40H42O14/c1-49-31-13-21(5-7-29(31)41)17-39(47)25(19-53-37(39)45)9-23-11-27(35(43)33(15-23)51-3)28-12-24(16-34(52-4)36(28)44)10-26-20-54-38(46)40(26,48)18-22-6-8-30(42)32(14-22)50-2/h5-8,11-16,25-26,41-44,47-48H,9-10,17-20H2,1-4H3/t25-,26-,39-,40-/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 Bis-5,5-nortrachelogenin

The roots of Wikstroemia indica

Biological Activity of Bis-5,5-nortrachelogenin

TargetsNO

Bis-5,5-nortrachelogenin Dilution Calculator

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Bis-5,5-nortrachelogenin Molarity Calculator

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Preparing Stock Solutions of Bis-5,5-nortrachelogenin

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.339 mL 6.6952 mL 13.3905 mL 26.7809 mL 33.4762 mL
5 mM 0.2678 mL 1.339 mL 2.6781 mL 5.3562 mL 6.6952 mL
10 mM 0.1339 mL 0.6695 mL 1.339 mL 2.6781 mL 3.3476 mL
50 mM 0.0268 mL 0.1339 mL 0.2678 mL 0.5356 mL 0.6695 mL
100 mM 0.0134 mL 0.067 mL 0.1339 mL 0.2678 mL 0.3348 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 Bis-5,5-nortrachelogenin

Lignans from the roots of Wikstroemia indica and their DPPH radical scavenging and nitric oxide inhibitory activities.[Pubmed:16205001]

Chem Pharm Bull (Tokyo). 2005 Oct;53(10):1348-51.

In our investigation of in vitro anti-allergic screening of medicinal herbal extracts, the ethyl acetate extract of the root of Wikstroemia indica was observed to inhibit nitric oxide (NO) production in a lipopolysaccharide (LPS) and recombinant mouse interferon-gamma (IFN-gamma) activated murine macrophage-like cell line, RAW 264.7. Fractionation of the active extract led to the isolation of two new lignan dimer Bis-5,5-nortrachelogenin (1) and bis-5,5'-nortrachelogenin (2), and three known lignans. Compound 1 and lirioresinol B (5) inhibited NO production with IC50 values at 48.6 and 53.5 microM, respectively. Compound 5 also showed free radical scavenging effect on 1,1-diphenyl-2-picrylhydrazil (DPPH) at IC50 values at 19.5 microM.

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