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6-Deoxyisojacareubin

CAS# 26486-92-0

6-Deoxyisojacareubin

Catalog No. BCN7723----Order now to get a substantial discount!

Product Name & Size Price Stock
6-Deoxyisojacareubin:5mg Please Inquire In Stock
6-Deoxyisojacareubin:10mg Please Inquire In Stock
6-Deoxyisojacareubin:20mg Please Inquire In Stock
6-Deoxyisojacareubin:50mg Please Inquire In Stock

Quality Control of 6-Deoxyisojacareubin

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Chemical structure

6-Deoxyisojacareubin

3D structure

Chemical Properties of 6-Deoxyisojacareubin

Cas No. 26486-92-0 SDF Download SDF
PubChem ID 5464641 Appearance Powder
Formula C18H14O5 M.Wt 310.30
Type of Compound Xanthones Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 6,11-dihydroxy-3,3-dimethylpyrano[2,3-c]xanthen-7-one
SMILES CC1(C=CC2=C3C(=C(C=C2O1)O)C(=O)C4=C(O3)C(=CC=C4)O)C
Standard InChIKey XWRLBJDPJRDNKF-UHFFFAOYSA-N
Standard InChI InChI=1S/C18H14O5/c1-18(2)7-6-9-13(23-18)8-12(20)14-15(21)10-4-3-5-11(19)16(10)22-17(9)14/h3-8,19-20H,1-2H3
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 6-Deoxyisojacareubin

The stem-barks of Garcinia nervosa.

Biological Activity of 6-Deoxyisojacareubin

Description1. 6-Deoxyisojacareubin has antimicrobial activity. 2. 6-Deoxyisojacareubin shows moderate inhibitory activity against the QGY-7703 cell line, with the IC50 value of 9.65 uM. 3. 6-Deoxyisojacareubin possesses potency in the inhibition of protein kinase C (PKC).
TargetsPKC | Antifection

6-Deoxyisojacareubin Dilution Calculator

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6-Deoxyisojacareubin Molarity Calculator

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Preparing Stock Solutions of 6-Deoxyisojacareubin

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.2227 mL 16.1134 mL 32.2269 mL 64.4538 mL 80.5672 mL
5 mM 0.6445 mL 3.2227 mL 6.4454 mL 12.8908 mL 16.1134 mL
10 mM 0.3223 mL 1.6113 mL 3.2227 mL 6.4454 mL 8.0567 mL
50 mM 0.0645 mL 0.3223 mL 0.6445 mL 1.2891 mL 1.6113 mL
100 mM 0.0322 mL 0.1611 mL 0.3223 mL 0.6445 mL 0.8057 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 6-Deoxyisojacareubin

A new pyranoxanthone from Garcinia nervosa.[Pubmed:28412841]

Nat Prod Res. 2017 Nov;31(21):2513-2519.

Phytochemical studies on the stem bark of Garcinia nervosa has resulted in the discovery of one new pyranoxanthone derivative, garner xanthone (1) and five other compounds, 1,5-dihydroxyxanthone (2), 6-Deoxyisojacareubin (3), 12b-hydroxy-des-D-garcigerrin A (4) stigmasterol (5), and beta-sitosterol (6). The structures of these compounds were elucidated with the aid of spectroscopic techniques, such as NMR and MS. The crude extracts of the plant were assessed for their antimicrobial activity.

Efficient total synthesis and biological activities of 6-deoxyisojacareubin.[Pubmed:23519477]

Arch Pharm (Weinheim). 2013 Apr;346(4):314-20.

6-Deoxyisojacareubin was directly synthesized in a six-step route with an overall yield of about 20%. In this route, the excellent site selectivity of this Claisen rearrangement-cyclization reaction cascade was achieved by inserting a bulky p-tosyl group into the free 1-OH, and in the last step, some efficient demethylation methods were explored. Furthermore, all synthesized intermediates including 6-Deoxyisojacareubin were evaluated for their inhibitory activity against the QGY-7703 cell line. Of these, compound 1 and 6-Deoxyisojacareubin showed moderate activities with IC50 values of 39.61 and 9.65 microM, respectively, when compared to the positive control 5-fluorouracil with an IC50 value of 11.24 microM. Further investigation using non-radioactive detection of protein kinase C (PKC) suggested that these two compounds possessed potency in the inhibition of PKC.

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