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Nigrolineaxanthone V

CAS# 864516-31-4

Nigrolineaxanthone V

Catalog No. BCN4411----Order now to get a substantial discount!

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Quality Control of Nigrolineaxanthone V

Number of papers citing our products

Chemical structure

Nigrolineaxanthone V

3D structure

Chemical Properties of Nigrolineaxanthone V

Cas No. 864516-31-4 SDF Download SDF
PubChem ID 11553272 Appearance Yellow powder
Formula C24H24O6 M.Wt 408.5
Type of Compound Xanthones Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 7,12-dihydroxy-9-methoxy-2,2-dimethyl-10-(3-methylbut-2-enyl)pyrano[3,2-b]xanthen-6-one
SMILES CC(=CCC1=C(C=C(C2=C1OC3=C(C4=C(C=CC(O4)(C)C)C=C3C2=O)O)O)OC)C
Standard InChIKey OCYZJBDJUYIHMM-UHFFFAOYSA-N
Standard InChI InChI=1S/C24H24O6/c1-12(2)6-7-14-17(28-5)11-16(25)18-19(26)15-10-13-8-9-24(3,4)30-21(13)20(27)23(15)29-22(14)18/h6,8-11,25,27H,7H2,1-5H3
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 Nigrolineaxanthone V

The fruits of Garcinia mangostana L.

Biological Activity of Nigrolineaxanthone V

DescriptionStandard reference
In vitro

Polyisoprenylated benzophenone and xanthone constituents of the bark of Garcinia cochinchinensis.[Reference: WebLink]

Phytochemistry Letters.2013 May; 6(2):224–227.


METHODS AND RESULTS:
A new polyisoprenylated benzophenone, guttiferone T, three other benzophenones, (−)-30-epi-cambogin, (−)-guttiferone G and (−)-garcinialiptone A, together with six xanthones, tovophyllin B, Nigrolineaxanthone V, pedunxanthone A, tovophyllin A, parvifolixanthone B and dulxanthone A, were isolated from the bark of Garcinia cochinchinensis. Their structures were elucidated using spectroscopic methods, mainly 1-D and 2-D NMR.
CONCLUSIONS:
Three of the polyisoprenylated benzophenone were tested for their cytotoxicity towards two human cancer cell lines, Hela and MCF-7, and exhibited weak activity.

Nigrolineaxanthone V Dilution Calculator

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Nigrolineaxanthone V Molarity Calculator

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Preparing Stock Solutions of Nigrolineaxanthone V

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.448 mL 12.2399 mL 24.4798 mL 48.9596 mL 61.1995 mL
5 mM 0.4896 mL 2.448 mL 4.896 mL 9.7919 mL 12.2399 mL
10 mM 0.2448 mL 1.224 mL 2.448 mL 4.896 mL 6.12 mL
50 mM 0.049 mL 0.2448 mL 0.4896 mL 0.9792 mL 1.224 mL
100 mM 0.0245 mL 0.1224 mL 0.2448 mL 0.4896 mL 0.612 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 Nigrolineaxanthone V

Polyisoprenylated benzophenone and xanthone constituents of the bark of Garcinia cochinchinensis.

Phytochemistry Letters.2013 May; 6(2):224–227.

A new polyisoprenylated benzophenone, guttiferone T, three other benzophenones, (−)-30-epi-cambogin, (−)-guttiferone G and (−)-garcinialiptone A, together with six xanthones, tovophyllin B, Nigrolineaxanthone V, pedunxanthone A, tovophyllin A, parvifolixanthone B and dulxanthone A, were isolated from the bark of Garcinia cochinchinensis. Their structures were elucidated using spectroscopic methods, mainly 1-D and 2-D NMR. Three of the polyisoprenylated benzophenone were tested for their cytotoxicity towards two human cancer cell lines, Hela and MCF-7, and exhibited weak activity.

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