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Tabernaecorymbosine A

CAS# 1262306-81-9

Tabernaecorymbosine A

Catalog No. BCN0464----Order now to get a substantial discount!

Product Name & Size Price Stock
Tabernaecorymbosine A: 5mg $1173 In Stock
Tabernaecorymbosine A: 10mg Please Inquire In Stock
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Quality Control of Tabernaecorymbosine A

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Chemical structure

Tabernaecorymbosine A

Chemical Properties of Tabernaecorymbosine A

Cas No. 1262306-81-9 SDF Download SDF
PubChem ID N/A Appearance Powder
Formula C44H54N4O6 M.Wt 734.9
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
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.

Tabernaecorymbosine A Dilution Calculator

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Tabernaecorymbosine A Molarity Calculator

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Preparing Stock Solutions of Tabernaecorymbosine A

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 1.3607 mL 6.8036 mL 13.6073 mL 27.2146 mL 34.0182 mL
5 mM 0.2721 mL 1.3607 mL 2.7215 mL 5.4429 mL 6.8036 mL
10 mM 0.1361 mL 0.6804 mL 1.3607 mL 2.7215 mL 3.4018 mL
50 mM 0.0272 mL 0.1361 mL 0.2721 mL 0.5443 mL 0.6804 mL
100 mM 0.0136 mL 0.068 mL 0.1361 mL 0.2721 mL 0.3402 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 Tabernaecorymbosine A

Taburnaemines A-I, Cytotoxic Vobasinyl-Iboga-Type Bisindole Alkaloids from Tabernaemontana corymbosa.[Pubmed:29319316]

J Nat Prod. 2018 Mar 23;81(3):562-571.

Nineteen vobasinyl-ibogan-type bisindole alkaloids, including nine new compounds, taburnaemines A-I (1-9), were isolated from the twigs and leaves of Tabernaemontana corymbosa. The structures and absolute configurations of the new alkaloids were determined by a combination of MS, NMR, and ECD analyses. Alkaloids 1-5 contain a rare 1,3-oxazinane moiety in the vobasinyl unit, while 6 has an uncommon 1,3-oxazolidine moiety in the iboga unit. The absolute configurations of alkaloid 1 and the known alkaloid Tabernaecorymbosine A (10) were confirmed by single-crystal X-ray diffraction analysis. All of the bisindole alkaloids, except 2 and 16'-decarbomethoxyTabernaecorymbosine A (14), showed antiproliferative activity (IC50 2.6-9.8 muM) against several human cancer cell lines, including A-549, MDA-MB-231, MCF-7, KB, and P-glycoprotein-overexpressing multidrug-resistant KB cells. The preliminary structure-activity relationship correlations are also discussed.

New vobasinyl-ibogan type bisindole alkaloids from Tabernaemontana corymbosa.[Pubmed:25449423]

Fitoterapia. 2015 Jan;100:150-5.

Ten vobasinyl-ibogan type bisindole alkaloids, including three new ones, tabercorines A-C (1-3), and a new natural product, 17-acetyl-Tabernaecorymbosine A (4), were isolated from the twigs and leaves of Tabernaemontana corymbosa. Their structures were elucidated on the basis of spectroscopic data, and the NMR data of 17-acetyl-Tabernaecorymbosine A (4) was assigned and reported for the first time. The absolute configurations of 1-4 were determined by CD exciton chirality method. All new compounds were evaluated for in vitro cytotoxicity against various human cancer cell lines. Compounds 1 and 4 showed significant inhibitory effects with IC50 values comparable to those of cisplatin.

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