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2,6-Dimethoxy-1-acetonylquinol

CAS# 2215-96-5

2,6-Dimethoxy-1-acetonylquinol

Catalog No. BCN5052----Order now to get a substantial discount!

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2,6-Dimethoxy-1-acetonylquinol: 5mg $477 In Stock
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Quality Control of 2,6-Dimethoxy-1-acetonylquinol

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Chemical structure

2,6-Dimethoxy-1-acetonylquinol

3D structure

Chemical Properties of 2,6-Dimethoxy-1-acetonylquinol

Cas No. 2215-96-5 SDF Download SDF
PubChem ID 241783 Appearance Yellow powder
Formula C11H14O5 M.Wt 226.2
Type of Compound Quinones Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 4-hydroxy-3,5-dimethoxy-4-(2-oxopropyl)cyclohexa-2,5-dien-1-one
SMILES CC(=O)CC1(C(=CC(=O)C=C1OC)OC)O
Standard InChIKey KMNCHTPRXWQOIZ-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 2,6-Dimethoxy-1-acetonylquinol

The barks of Ailanthus altissima

Biological Activity of 2,6-Dimethoxy-1-acetonylquinol

Description1. 2,6-Dimethoxy-1-acetonylquinol shows varying degrees of in vitro antimalarial activity against Plasmodium falciparum. 2. 2,6-Dimethoxy-1-acetonylquinol is devoid of significant cytotoxicity to the human oral epidermoid KB cancer cell line.
TargetsAntifection

2,6-Dimethoxy-1-acetonylquinol Dilution Calculator

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2,6-Dimethoxy-1-acetonylquinol Molarity Calculator

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Preparing Stock Solutions of 2,6-Dimethoxy-1-acetonylquinol

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 4.4209 mL 22.1043 mL 44.2087 mL 88.4173 mL 110.5217 mL
5 mM 0.8842 mL 4.4209 mL 8.8417 mL 17.6835 mL 22.1043 mL
10 mM 0.4421 mL 2.2104 mL 4.4209 mL 8.8417 mL 11.0522 mL
50 mM 0.0884 mL 0.4421 mL 0.8842 mL 1.7683 mL 2.2104 mL
100 mM 0.0442 mL 0.221 mL 0.4421 mL 0.8842 mL 1.1052 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 2,6-Dimethoxy-1-acetonylquinol

Antimalarial compounds from Grewia bilamellata.[Pubmed:16562832]

J Nat Prod. 2006 Mar;69(3):346-50.

Bioassay-directed fractionation led to the isolation of 12 compounds from a sample of the dried leaves, twigs, and stems of Grewia bilamellata. Five of the isolates, 3alpha,20-lupandiol (1), grewin (2), nitidanin (4), 2alpha,3beta-dihydroxy-olean-12-en-28-oic acid (5), and 2,6-Dimethoxy-1-acetonylquinol (6), showed varying degrees of in vitro antimalarial activity against Plasmodium falciparum, but were devoid of significant cytotoxicity to the human oral epidermoid KB cancer cell line. Of the 12 isolates, compounds 1, 2, and 3 (bilagrewin) were determined to be a new triterpene, a new coumarinolignan, and a new neolignan, respectively. Other known compounds isolated in this study were 8-O-4' neolignan guaiacylglycerol-beta-coniferyl ether isomers (threo and erythro), cleomiscosin D, icariol A(2), ciwujiatone, and daucosterol. The structures of 1-3 were elucidated and identified on the basis of spectroscopic data including 1D and 2D NMR analysis.

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