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9-Methoxycanthin-6-one-N-oxide

CAS# 137739-74-3

9-Methoxycanthin-6-one-N-oxide

Catalog No. BCN2994----Order now to get a substantial discount!

Product Name & Size Price Stock
9-Methoxycanthin-6-one-N-oxide: 5mg Please Inquire In Stock
9-Methoxycanthin-6-one-N-oxide: 10mg Please Inquire In Stock
9-Methoxycanthin-6-one-N-oxide: 20mg Please Inquire Please Inquire
9-Methoxycanthin-6-one-N-oxide: 50mg Please Inquire Please Inquire
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Quality Control of 9-Methoxycanthin-6-one-N-oxide

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Chemical structure

9-Methoxycanthin-6-one-N-oxide

3D structure

Chemical Properties of 9-Methoxycanthin-6-one-N-oxide

Cas No. 137739-74-3 SDF Download SDF
PubChem ID 44593495 Appearance Yellow powder
Formula C15H10N2O3 M.Wt 266.3
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
SMILES COC1=CC2=C(C=C1)C3=C4N2C(=O)C=CC4=[N+](C=C3)[O-]
Standard InChIKey IADUHWGVUSHTRQ-UHFFFAOYSA-N
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 9-Methoxycanthin-6-one-N-oxide

The barks of Ailanthus altissima

Biological Activity of 9-Methoxycanthin-6-one-N-oxide

Description1. 9-Methoxycanthin-6-one-N-oxide shows cytotoxic activity against a panel of cell lines comprising a number of human cancer cell types.

9-Methoxycanthin-6-one-N-oxide Dilution Calculator

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9-Methoxycanthin-6-one-N-oxide Molarity Calculator

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Preparing Stock Solutions of 9-Methoxycanthin-6-one-N-oxide

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.7552 mL 18.7758 mL 37.5516 mL 75.1033 mL 93.8791 mL
5 mM 0.751 mL 3.7552 mL 7.5103 mL 15.0207 mL 18.7758 mL
10 mM 0.3755 mL 1.8776 mL 3.7552 mL 7.5103 mL 9.3879 mL
50 mM 0.0751 mL 0.3755 mL 0.751 mL 1.5021 mL 1.8776 mL
100 mM 0.0376 mL 0.1878 mL 0.3755 mL 0.751 mL 0.9388 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 9-Methoxycanthin-6-one-N-oxide

Cytotoxic and antimalarial constituents of the roots of Eurycoma longifolia.[Pubmed:1800638]

J Nat Prod. 1991 Sep-Oct;54(5):1360-7.

By bioactivity-directed fractionation, five cytotoxic constituents have been characterized from the roots of Eurycoma longifolia collected in Kalimantan, Indonesia. Four canthin-6-one alkaloids, namely, 9-methoxycanthin-6-one, 9-Methoxycanthin-6-one-N-oxide, 9-hydroxycanthin-6-one, and 9-hydroxycanthin-6-one-N-oxide, and one quassinoid, eurycomanone, were found to be cytotoxic principles. Each of these compounds was evaluated against a panel of cell lines comprising a number of human cancer cell types [breast, colon, fibrosarcoma, lung, melanoma, KB, and KB-V1 (a multi-drug resistant cell line derived from KB)] and murine lymphocytic leukemia (P-388). The canthin-6-ones 1-4 were found to be active with all cell lines tested except for the KB-V1 cell line. Eurycomanone was inactive against murine lymphocytic leukemia (P-388) but was significantly active against the human cell lines tested. Two additional isolates, the beta-carboline alkaloids beta-carboline-1-propionic acid and 7-methoxy-beta-carboline-1-propionic acid, were not significantly active with these cultured cells. However, compounds 5 and 7 were found to demonstrate significant antimalarial activity as judged by studies conducted with cultured Plasmodium falciparum strains. The structures of the novel compounds 2-4 and 7 were established by spectral and chemical methods.

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