8-DeacetylyunaconitineCAS# 93460-55-0 |
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| Cas No. | 93460-55-0 | SDF | Download SDF |
| PubChem ID | 134714924 | Appearance | Powder |
| Formula | C33H47NO10 | M.Wt | 617.73 |
| Type of Compound | Alkaloids | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | [(1S,2R,3R,4R,5S,6S,8R,10R,13R,14R,16S,17S,18R)-11-ethyl-5,8,14-trihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate | ||
| SMILES | CCN1CC2(C(CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)O)OC)OC)O)COC | ||
| Standard InChIKey | DHVYLCVNTWPXSI-PLQCILJTSA-N | ||
| Standard InChI | InChI=1S/C33H47NO10/c1-7-34-15-30(16-39-2)20(35)12-21(41-4)33-19-13-31(37)22(42-5)14-32(38,24(27(33)34)25(43-6)26(30)33)23(19)28(31)44-29(36)17-8-10-18(40-3)11-9-17/h8-11,19-28,35,37-38H,7,12-16H2,1-6H3/t19-,20-,21+,22+,23-,24?,25+,26-,27-,28-,30+,31+,32-,33+/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 | 8-Deacetylyunaconitine is a natural product from Aconitum Vilmorinian Radix. |
| Structure Identification | Zhong Yao Cai. 2015 May;38(5):988-91.Chemical Constituents from Processed Products of Aconitum Vilmoriniani Radix.[Pubmed: 26767293]To investigate the chemical constituents of the processed products of Aconitum Vilmorinian Radix.
J Sep Sci. 2013 Aug;36(16):2680-5.Accelerated solvent extraction and pH-zone-refining counter-current chromatographic purification of yunaconitine and 8-deacetylyunaconitine from Aconitum vilmorinianum Kom.[Pubmed: 23784883]
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8-Deacetylyunaconitine Dilution Calculator
8-Deacetylyunaconitine Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 1.6188 mL | 8.0942 mL | 16.1883 mL | 32.3766 mL | 40.4708 mL |
| 5 mM | 0.3238 mL | 1.6188 mL | 3.2377 mL | 6.4753 mL | 8.0942 mL |
| 10 mM | 0.1619 mL | 0.8094 mL | 1.6188 mL | 3.2377 mL | 4.0471 mL |
| 50 mM | 0.0324 mL | 0.1619 mL | 0.3238 mL | 0.6475 mL | 0.8094 mL |
| 100 mM | 0.0162 mL | 0.0809 mL | 0.1619 mL | 0.3238 mL | 0.4047 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 from Processed Products of Aconitum Vilmoriniani Radix].[Pubmed:26767293]
Zhong Yao Cai. 2015 May;38(5):988-91.
OBJECTIVE: To investigate the chemical constituents of the processed products of Aconitum Vilmorinian Radix. METHODS: The constituents were isolated by repeated column chromatography over silica gel, alumina and RP-C18 as well as recrystallization. The structures were elucidated on the basis of spectral analysis and physicochemical properties. RESULTS: Ten compounds were obtained from the methanol extract, and they were identified as yunaconitine (1), 8-deacetyl-yunaconitine (2), geniculatine C (3), vilmorrianine B (4), vilmorrianine C(5), vilmorrianine D (6), talatisamine (7), beta-sitosterol (8), beta-daucosterol (9) and beta-sitosterol acetate (10). CONCLUSION: All compounds are obtained from the processed products of Aconitum Vilmoriniani Radix for the first time.
Accelerated solvent extraction and pH-zone-refining counter-current chromatographic purification of yunaconitine and 8-deacetylyunaconitine from Aconitum vilmorinianum Kom.[Pubmed:23784883]
J Sep Sci. 2013 Aug;36(16):2680-5.
This study aimed to seek an efficient method to extract and purify yunaconitine and 8-Deacetylyunaconitine from Aconitum vilmorinianum Kom. by accelerated solvent extraction combined with pH-zone-refining counter-current chromatography. The major extraction parameters for accelerated solvent extraction were optimized by an orthogonal test design L9 (3)(4). Then a separation and purification method was established using pH-zone-refining counter-current chromatography with a two-phase solvent system composed of petroleum ether/ethyl acetate/methanol/water (5:5:2:8, v/v) with 10 mM triethylamine in the upper phase and 10 mM HCl in the lower phase. From 2 g crude extract, 224 mg of 8-Deacetylyunaconitine (I) and 841 mg of yunaconitine (II) were obtained with a purity of over 98.0%. The chemical structures were identified by ESI-MS and (1)H and (13)C NMR spectroscopy.
