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Dimeric coniferyl acetate

CAS# 184046-40-0

Dimeric coniferyl acetate

Catalog No. BCN1148----Order now to get a substantial discount!

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Quality Control of Dimeric coniferyl acetate

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Chemical structure

Dimeric coniferyl acetate

3D structure

Chemical Properties of Dimeric coniferyl acetate

Cas No. 184046-40-0 SDF Download SDF
PubChem ID 44584272 Appearance Powder
Formula C24H26O8 M.Wt 442.5
Type of Compound Lignans Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name [(E)-3-[(2S,3R)-3-(acetyloxymethyl)-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]prop-2-enyl] acetate
SMILES CC(=O)OCC=CC1=CC2=C(C(=C1)OC)OC(C2COC(=O)C)C3=CC(=C(C=C3)O)OC
Standard InChIKey TYXVTGSQLKCKCF-FDTLDTTQSA-N
Standard InChI InChI=1S/C24H26O8/c1-14(25)30-9-5-6-16-10-18-19(13-31-15(2)26)23(32-24(18)22(11-16)29-4)17-7-8-20(27)21(12-17)28-3/h5-8,10-12,19,23,27H,9,13H2,1-4H3/b6-5+/t19-,23+/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 Dimeric coniferyl acetate

The herbs of Jatropha integerrima

Biological Activity of Dimeric coniferyl acetate

Description1. Dimeric coniferyl acetate shows strong NO inhibition with IC50 values of 27.1 uM in lipopolysacchalide (LPS)-activated murine macrophage-like J774.1 cells. 2. Dimeric coniferyl acetate exhibits significant inhibitory effects on the nitric oxide production in lipopolysaccharide activated C57BL6/J mouse macrophages.
TargetsNO

Dimeric coniferyl acetate Dilution Calculator

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Dimeric coniferyl acetate Molarity Calculator

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Preparing Stock Solutions of Dimeric coniferyl acetate

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.2599 mL 11.2994 mL 22.5989 mL 45.1977 mL 56.4972 mL
5 mM 0.452 mL 2.2599 mL 4.5198 mL 9.0395 mL 11.2994 mL
10 mM 0.226 mL 1.1299 mL 2.2599 mL 4.5198 mL 5.6497 mL
50 mM 0.0452 mL 0.226 mL 0.452 mL 0.904 mL 1.1299 mL
100 mM 0.0226 mL 0.113 mL 0.226 mL 0.452 mL 0.565 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 Dimeric coniferyl acetate

Five new compounds from Rhododendron mariae Hance.[Pubmed:24320934]

J Asian Nat Prod Res. 2014 Jan;16(1):1-10.

Five new compounds (-)-(7R,8S,7'R,8'S)-4,9,4',9'-tetrahydroxy-3,3'-dimethoxy-7,7'-epoxylignan 9-O-beta-d-xylopyranoside (1), (-)-(7'R,8'S)-5'-methoxyl(Dimeric coniferyl acetate) (2), (+)-(1R,2S)-1,2-bis(4-hydroxy-3-methoxyphenyl)-3-acetyl-1,3-propanediol (3), (-)-3-((2R,3R)-2-ethoxy-3-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl)pr opan-1-ol (4), and (+)-3-((2S,3S)-2-ethoxy-3-(hydroxymethyl)-7-methoxy-2,3-dihydrobenzofuran-5-yl)pr opan-1-ol (5), together with 12 known compounds, were isolated from an ethanol extract of the dried stems of Rhododendron mariae Hance. Their structures were elucidated by NMR, HR-MS, CD, ORD experiments and chemical methods. Compounds 2, 3, 6, and 17 exhibited significant inhibitory effects on the nitric oxide production in lipopolysaccharide activated C57BL6/J mouse macrophages.

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