Paucinervin A

CAS# 1243249-16-2

Paucinervin A

2D Structure

Catalog No. BCN7308----Order now to get a substantial discount!

Product Name & Size Price Stock
Paucinervin A: 5mg $1012 In Stock
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Quality Control of Paucinervin A

3D structure

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Paucinervin A

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Chemical Properties of Paucinervin A

Cas No. 1243249-16-2 SDF Download SDF
PubChem ID 52949770 Appearance Powder
Formula C24H26O7 M.Wt 426.46
Type of Compound Xanthones Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 2,7,9-trihydroxy-1-methoxy-3,8-bis(3-methylbut-2-enyl)benzo[b][1,4]benzodioxepin-6-one
SMILES CC(=CCC1=CC2=C(C(=C1O)OC)OC3=CC(=C(C(=C3C(=O)O2)O)CC=C(C)C)O)C
Standard InChIKey CZKGIKZOHGKQSQ-UHFFFAOYSA-N
Standard InChI InChI=1S/C24H26O7/c1-12(2)6-8-14-10-18-22(23(29-5)20(14)26)30-17-11-16(25)15(9-7-13(3)4)21(27)19(17)24(28)31-18/h6-7,10-11,25-27H,8-9H2,1-5H3
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 Paucinervin A

The leaves of Garcinia paucinervis.

Biological Activity of Paucinervin A

Description1. Paucinervin A has inhibitory effect against HeLa cell growth, with the IC50 value of 29.5 microM.

Paucinervin A Dilution Calculator

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Paucinervin A Molarity Calculator

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Preparing Stock Solutions of Paucinervin A

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.3449 mL 11.7244 mL 23.4489 mL 46.8977 mL 58.6221 mL
5 mM 0.469 mL 2.3449 mL 4.6898 mL 9.3795 mL 11.7244 mL
10 mM 0.2345 mL 1.1724 mL 2.3449 mL 4.6898 mL 5.8622 mL
50 mM 0.0469 mL 0.2345 mL 0.469 mL 0.938 mL 1.1724 mL
100 mM 0.0234 mL 0.1172 mL 0.2345 mL 0.469 mL 0.5862 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 Paucinervin A

Identification and evaluation of apoptotic compounds from Garcinia paucinervis.[Pubmed:20594858]

Bioorg Med Chem. 2010 Jul 15;18(14):4957-64.

Four new compounds, paucinervins A-D (1-4), and 15 known ones were isolated from the leaves of Garcinia paucinervis. The structures of the new compounds were elucidated by spectroscopic evidences. All of the 19 compounds were evaluated for their apoptosis-inducing effects using HeLa-C3 cells which have been genetically engineered to possess a fluorescent biosensor capable of detecting caspase-3 activation. Eight of them were found to activate caspase-3 in HeLa-C3 cells within 72 h at the concentration of 25 microM. Moreover, the values of IC50 were measured for all four new compounds on HeLa cells using the MTT assay. Among them, compound 2 (paucinervin B) had the lowest IC50 value of 9.5 microM, while the other three new compounds had much higher IC50 values of 29.5, 52.5, and 95.6 microM, respectively. This result shows that paucinervin B has the strongest inhibitory effect against HeLa cell growth among these four newly identified paucinervins and it may have the potential to be developed into a new anticancer candidate.

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