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Echitoveniline

CAS# 72855-79-9

Echitoveniline

2D Structure

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Quality Control of Echitoveniline

3D structure

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Echitoveniline

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Chemical Properties of Echitoveniline

Cas No. 72855-79-9 SDF Download SDF
PubChem ID 134714943 Appearance Powder
Formula C31H36N2O7 M.Wt 548.63
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name methyl (1R,12R,19R)-12-[(1R)-1-(3,4,5-trimethoxybenzoyl)oxyethyl]-8,16-diazapentacyclo[10.6.1.01,9.02,7.016,19]nonadeca-2,4,6,9-tetraene-10-carboxylate
SMILES CC(C12CCCN3C1C4(CC3)C5=CC=CC=C5NC4=C(C2)C(=O)OC)OC(=O)C6=CC(=C(C(=C6)OC)OC)OC
Standard InChIKey YEMKFBSUDUKXBV-JZGDGXNWSA-N
Standard InChI InChI=1S/C31H36N2O7/c1-18(40-27(34)19-15-23(36-2)25(38-4)24(16-19)37-3)30-11-8-13-33-14-12-31(29(30)33)21-9-6-7-10-22(21)32-26(31)20(17-30)28(35)39-5/h6-7,9-10,15-16,18,29,32H,8,11-14,17H2,1-5H3/t18-,29+,30+,31+/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 Echitoveniline

The fruits and leaves of Alstonia venenata R.Br.

Biological Activity of Echitoveniline

DescriptionEchitoveniline is a natural product from Alstonia venenata R.Br.

Protocol of Echitoveniline

Structure Identification
Tetrahedron, 1979, 35(9):1151-1157.

Alkaloids of Alstonia venenata R.Br.[Reference: WebLink]


METHODS AND RESULTS:
Structures and absolute stereochemistry of (-)-Echitoveniline, (-)-11-methoxyEchitoveniline and (-)-11-methoxyechitovenedine, three new indole alkaloids of the vincadifformine type, isolated from the fruits and leaves of Alstonia venenata R.Br., have been established as 3b, 3c and 3d, respectively, on the basis of spectral and chemical evidence.
CONCLUSIONS:
A plausible mechanism of the LAH reduction of the δ-lactones8b and8c to the corresponding diols 9b and 9c has been discussed.

Echitoveniline Dilution Calculator

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Echitoveniline Molarity Calculator

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Preparing Stock Solutions of Echitoveniline

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.8227 mL 9.1136 mL 18.2272 mL 36.4544 mL 45.5681 mL
5 mM 0.3645 mL 1.8227 mL 3.6454 mL 7.2909 mL 9.1136 mL
10 mM 0.1823 mL 0.9114 mL 1.8227 mL 3.6454 mL 4.5568 mL
50 mM 0.0365 mL 0.1823 mL 0.3645 mL 0.7291 mL 0.9114 mL
100 mM 0.0182 mL 0.0911 mL 0.1823 mL 0.3645 mL 0.4557 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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References on Echitoveniline

Alkaloids of Alstonia venenata R.Br.

Tetrahedron, 1979, 35(9):1151-1157.

Structures and absolute stereochemistry of (-)-Echitoveniline, (-)-11-methoxyEchitoveniline and (-)-11-methoxyechitovenedine, three new indole alkaloids of the vincadifformine type, isolated from the fruits and leaves of Alstonia venenata R.Br., have been established as 3b, 3c and 3d, respectively, on the basis of spectral and chemical evidence. A plausible mechanism of the LAH reduction of the δ-lactones8b and8c to the corresponding diols 9b and 9c has been discussed.

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