Indaconitine

CAS# 4491-19-4

Indaconitine

2D Structure

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Indaconitine: 5mg $98 In Stock
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Quality Control of Indaconitine

3D structure

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Indaconitine

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Chemical Properties of Indaconitine

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.
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 Indaconitine

The root of Aconitum carmichaeli Debx.

Biological Activity of Indaconitine

DescriptionIndaconitine is a natural product from Aconitum hemsleyanum PRITZ.

Protocol of Indaconitine

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.
METHODS AND RESULTS:
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 Dilution Calculator

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Indaconitine Molarity Calculator

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Preparing Stock Solutions of Indaconitine

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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Background on Indaconitine

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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References on Indaconitine

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).

Description

Indaconitine is a natural product.

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