IsomagnololCAS# 87688-90-2 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
Cas No. | 87688-90-2 | SDF | Download SDF |
PubChem ID | 159137 | Appearance | White crystalline powder |
Formula | C18H18O2 | M.Wt | 266.33 |
Type of Compound | N/A | Storage | Desiccate at -20°C |
Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
Chemical Name | 4-prop-2-enyl-2-(4-prop-2-enylphenoxy)phenol | ||
SMILES | C=CCC1=CC=C(C=C1)OC2=C(C=CC(=C2)CC=C)O | ||
Standard InChIKey | ROPDWYIWHWKVLI-UHFFFAOYSA-N | ||
Standard InChI | InChI=1S/C18H18O2/c1-3-5-14-7-10-16(11-8-14)20-18-13-15(6-4-2)9-12-17(18)19/h3-4,7-13,19H,1-2,5-6H2 | ||
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. |
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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. |
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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. |
Isomagnolol Dilution Calculator
Isomagnolol Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 3.7547 mL | 18.7737 mL | 37.5474 mL | 75.0948 mL | 93.8685 mL |
5 mM | 0.7509 mL | 3.7547 mL | 7.5095 mL | 15.019 mL | 18.7737 mL |
10 mM | 0.3755 mL | 1.8774 mL | 3.7547 mL | 7.5095 mL | 9.3869 mL |
50 mM | 0.0751 mL | 0.3755 mL | 0.7509 mL | 1.5019 mL | 1.8774 mL |
100 mM | 0.0375 mL | 0.1877 mL | 0.3755 mL | 0.7509 mL | 0.9387 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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Anti-hepatitis B virus lignans from the root of Streblus asper.[Pubmed:23434030]
Bioorg Med Chem Lett. 2013 Apr 1;23(7):2238-44.
Four new lignans, strebluslignanol F (1), (7'R,8'S,7''R,8''S)-erythro-strebluslignanol G (2), isomagnaldehyde (3) and isostrebluslignanaldehyde (4), along with 12 known lignans (5-16) were isolated from the ethyl acetate-soluble part of MeOH extract of the root of Streblus asper. Their structures were elucidated through various spectroscopic methods, including 1D NMR ((1)H NMR, (13)C NMR), 2D NMR (HMQC, HMBC and NOESY) and HRMS. The stereochemistry at the chiral centers was determined using CD spectra, as well as analyses of coupling constants and optical rotation data. The isolated lignans were evaluated for their anti-HBV activities in vitro using the HBV transfected HepG2.2.15 cell line. The most active lignans, (7'R,8'S,7''R,8''S)-erythro-strebluslignanol G, magnolol, Isomagnolol and isolariciresinol, exhibited significant anti-HBV activities with IC50 values of 1.58, 2.03, 10.34 and 3.67 muM, respectively, for HBsAg with no cytotoxicity, and of 3.24, 3.76, 8.83 and 14.67 muM, respectively, for HBeAg with no cytotoxicity. (7'R,8'S,7''R,8''S)-erythro-Strebluslignanol G and magnolol showed significant anti-HBV activities to inhibit the replication of HBV DNA with the IC50 values of 9.02 and 8.67 muM, respectively.
Neolignans from the fruits of Magnolia obovata and their inhibition effect on NO production in LPS-induced RAW 264.7 cells.[Pubmed:23970426]
Planta Med. 2013 Sep;79(14):1335-40.
Three new neolignans, named 9-methoxyobovatol (6), magnobovatol (7), and 2-hydroxyobovaaldehyde (9), along with six known ones, magnolol (1), honokiol (2), Isomagnolol (3), obovatol (4), obovatal (5), and obovaaldehyde (8), were isolated from the fruits of Magnolia obovata using silica gel and ODS column chromatography. From the results of spectroscopic data including EIMS, IR, 1H- and 13C-NMR, DEPT, and 2D-NMR (gCOSY, gHSQC, gHMBC), the chemical structures were determined. All isolated compounds were evaluated for inhibition activity on nitric oxide production in LPS-induced RAW 264.7 cells, and compounds 1-4, 6, 7, and 9 showed significant activity with IC50 values of 15.8 +/- 0.3, 3.3 +/- 1.2, 14.1 +/- 0.9, 6.2 +/- 1.2, 14.8 +/- 2.3, 14.2 +/- 1.2, and 14.8 +/- 3.2 microM, respectively, without any visible toxic effect.