IndaconitineCAS# 4491-19-4 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
| Cas No. | 4491-19-4 | SDF | Download SDF |
| PubChem ID | 441740 | Appearance | White powder |
| Formula | C34H47NO10 | M.Wt | 629.82 |
| Type of Compound | Alkaloids | Storage | Desiccate at -20°C |
| Synonyms | 15-Deoxyaconitine | ||
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| SMILES | CCN1CC2(C(CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=CC=C7)O)OC)OC(=O)C)OC)OC)O)COC | ||
| Standard InChIKey | PHDZNMWTZQPAEW-ZIVNFORMSA-N | ||
| Standard InChI | InChI=1S/C34H47NO10/c1-7-35-16-31(17-40-3)21(37)13-22(41-4)34-20-14-32(39)23(42-5)15-33(45-18(2)36,25(28(34)35)26(43-6)27(31)34)24(20)29(32)44-30(38)19-11-9-8-10-12-19/h8-12,20-29,37,39H,7,13-17H2,1-6H3/t20-,21-,22+,23+,24-,25+,26+,27-,28?,29-,31+,32+,33-,34+/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. | ||
The root of Aconitum carmichaeli Debx.
| Description | Indaconitine is a natural product from Aconitum hemsleyanum PRITZ. |
| Structure Identification | Chem Pharm Bull (Tokyo). 2003 May;51(5):592-4.Hemsleyatine, a novel C19-diterpenoid alkaloid with 8-amino group from Aconitum hemsleyanum.[Pubmed: 12736463]The new compound hemsleyatine (1) was isolated along with four known C(19)-diterpenoid alkaloids: Indaconitine (4), yunaconitine (5), chasmanine (6), and talatisamine (7) from the roots of Aconitum hemsleyanum PRITZ. |
Indaconitine Dilution Calculator
Indaconitine Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 1.5878 mL | 7.9388 mL | 15.8776 mL | 31.7551 mL | 39.6939 mL |
| 5 mM | 0.3176 mL | 1.5878 mL | 3.1755 mL | 6.351 mL | 7.9388 mL |
| 10 mM | 0.1588 mL | 0.7939 mL | 1.5878 mL | 3.1755 mL | 3.9694 mL |
| 50 mM | 0.0318 mL | 0.1588 mL | 0.3176 mL | 0.6351 mL | 0.7939 mL |
| 100 mM | 0.0159 mL | 0.0794 mL | 0.1588 mL | 0.3176 mL | 0.3969 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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Indaconitine is a natural product.
References:
[1]. RE Gilman, et al.THE STRUCTURE OF INDACONITINE. Canadian Journal of Chemistry (Impact Factor: 1.01). 02/2011; 42(12):2700-2704.
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Hemsleyatine, a novel C19-diterpenoid alkaloid with 8-amino group from Aconitum hemsleyanum.[Pubmed:12736463]
Chem Pharm Bull (Tokyo). 2003 May;51(5):592-4.
The new compound hemsleyatine (1) was isolated along with four known C(19)-diterpenoid alkaloids: Indaconitine (4), yunaconitine (5), chasmanine (6), and talatisamine (7) from the roots of Aconitum hemsleyanum PRITZ. Structures were established by spectral analysis, including tow dimeusional (2D) NMR spectroscopy and a chemical method. Hemsleyatine (1) is the first C(19)-diterpenoid alkaloid bearing the 8-amino group. In addition, the assignments of some (13)C signals for pseudaconine (3) were revised by comparison with those of hemsleyatine (1).
Indaconitine is a natural product.
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