Shizukaol GCAS# 165171-11-9 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
Cas No. | 165171-11-9 | SDF | Download SDF |
PubChem ID | 122233413 | Appearance | Powder |
Formula | C40H44O14 | M.Wt | 748.77 |
Type of Compound | Sesquiterpenoids | Storage | Desiccate at -20°C |
Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
Chemical Name | methyl (2Z)-2-[(1S,9S,13E,18S,19S,21R,22S,23S,26S,28R,29S,30R,33R,36R)-9,18,30-trihydroxy-14,22,29-trimethyl-3,7,10,15,31-pentaoxo-2,6,11,16-tetraoxanonacyclo[16.15.3.125,29.01,23.04,34.019,21.022,36.026,28.033,37]heptatriaconta-4(34),13,25(37)-trien-32-ylidene]propanoate | ||
SMILES | CC1=CCOC(=O)C(CC(=O)OCC2=C3CC4C(C5CC5C4(COC1=O)O)(C6C3(C7C8=C(C6)C9CC9C8(C(C(=O)C7=C(C)C(=O)OC)O)C)OC2=O)C)O | ||
Standard InChIKey | VQIMOHFODDGHOJ-XEQPTWOZSA-N | ||
Standard InChI | InChI=1S/C40H44O14/c1-15-6-7-51-36(48)24(41)12-27(42)52-13-19-21-11-25-37(3,22-10-23(22)39(25,49)14-53-33(15)45)26-9-18-17-8-20(17)38(4)29(18)30(40(21,26)54-35(19)47)28(31(43)32(38)44)16(2)34(46)50-5/h6,17,20,22-26,30,32,41,44,49H,7-14H2,1-5H3/b15-6+,28-16-/t17-,20-,22-,23+,24+,25-,26+,30+,32+,37+,38+,39+,40+/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. |
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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. |
Description | Shizukaol G is a natural product from Chloranthus japonicus. |
Structure Identification | Chinese Traditional & Herbal Drugs, 2016 ,47(18):3169-3174.Chemical constituents in lindenane-type sesquiterpene dimers in roots of Chloranthus multistachys.[Reference: WebLink]
To study the chemical constituents contained in the ethanol extracts from the roots of Chloranthus multistachys. |
Shizukaol G Dilution Calculator
Shizukaol G Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 1.3355 mL | 6.6776 mL | 13.3552 mL | 26.7105 mL | 33.3881 mL |
5 mM | 0.2671 mL | 1.3355 mL | 2.671 mL | 5.3421 mL | 6.6776 mL |
10 mM | 0.1336 mL | 0.6678 mL | 1.3355 mL | 2.671 mL | 3.3388 mL |
50 mM | 0.0267 mL | 0.1336 mL | 0.2671 mL | 0.5342 mL | 0.6678 mL |
100 mM | 0.0134 mL | 0.0668 mL | 0.1336 mL | 0.2671 mL | 0.3339 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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Chemical constituents in lindenane-type sesquiterpene dimers in roots of Chloranthus multistachys.
Chinese Traditional & Herbal Drugs, 2016 ,47(18):3169-3174.
To study the chemical constituents contained in the ethanol extracts from the roots of Chloranthus multistachys. Methods: Twelve compounds were separated from the roots of C. multistachys and their structures were identified by using various chromatographic techniques. Results: The structures of the 12 lindenane-type sesquiterpene dimmers from the chloroform and ethyl acetate extract in the roots of C. multistachys were identified on the basis of physicochemical properties and spectral data as 9-O-β-glucopyranosylcycloshizukaol A (1), cycloshizukaol A (2), shizukaol B (3), shizukaol C (4), shizukaol D (5), shizukaol F (6), Shizukaol G (7), chloramultiol B (8), sarcandrolide B (9), sarglabolide I (10), 8-O-methyltianmushanol (11), and henriol B (12). Conclusion: Compounds 1, 7, and 9-12 are isolated from the roots C. multistachys for the first time and compounds 9 and 10 are obtained from the plants of Chloranthus Sw. for the first time.