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Methylenedihydrotanshinquinone

CAS# 126979-81-5

Methylenedihydrotanshinquinone

2D Structure

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Quality Control of Methylenedihydrotanshinquinone

3D structure

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Methylenedihydrotanshinquinone

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Chemical Properties of Methylenedihydrotanshinquinone

Cas No. 126979-81-5 SDF Download SDF
PubChem ID 102004770 Appearance Red powder
Formula C18H16O3 M.Wt 280.3
Type of Compound Diterpenoids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name (1R)-1-methyl-6-methylidene-2,7,8,9-tetrahydro-1H-naphtho[1,2-g][1]benzofuran-10,11-dione
SMILES CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4=C
Standard InChIKey UXXYCZFYFKWTPQ-JTQLQIEISA-N
Standard InChI InChI=1S/C18H16O3/c1-9-4-3-5-12-11(9)6-7-13-15(12)17(20)16(19)14-10(2)8-21-18(13)14/h6-7,10H,1,3-5,8H2,2H3/t10-/m0/s1
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 Methylenedihydrotanshinquinone

The roots of Salvia miltiorrhiza

Biological Activity of Methylenedihydrotanshinquinone

Description1. Methylenedihydrotanshinquinone has cytotoxic activity.

Methylenedihydrotanshinquinone Dilution Calculator

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Methylenedihydrotanshinquinone Molarity Calculator

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Preparing Stock Solutions of Methylenedihydrotanshinquinone

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 3.5676 mL 17.838 mL 35.6761 mL 71.3521 mL 89.1902 mL
5 mM 0.7135 mL 3.5676 mL 7.1352 mL 14.2704 mL 17.838 mL
10 mM 0.3568 mL 1.7838 mL 3.5676 mL 7.1352 mL 8.919 mL
50 mM 0.0714 mL 0.3568 mL 0.7135 mL 1.427 mL 1.7838 mL
100 mM 0.0357 mL 0.1784 mL 0.3568 mL 0.7135 mL 0.8919 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 Methylenedihydrotanshinquinone

From Bioprofiling and Characterization to Bioquantification of Natural Antibiotics by Direct Bioautography Linked to High-Resolution Mass Spectrometry: Exemplarily Shown for Salvia miltiorrhiza Root.[Pubmed:27766834]

Anal Chem. 2016 Nov 15;88(22):10979-10986.

Phytochemicals are promising agents in the development of new antibiotics. A streamlined strategy for rapid screening and reliable characterization of antibiotics in botanicals was demonstrated in contrast to the commonly applied chromatographic column fractionation followed by microtiter plate assay. Modern direct bioautography hyphenated to structure elucidation techniques is a straightforward bioanalytical tool, especially if microbiological assays were taken into account. At one go, lipophilic antimicrobials in Salvia miltiorrhiza root samples were analyzed using high-performance thin-layer chromatography (HPTLC) in direct combination with Aliivibrio fischeri and Bacillus subtilis bioassays. The most intense antimicrobials were characterized via HPTLC-high-resolution mass spectrometry. As proof of this streamlined strategy, dihydrotanshinone, cryptotanshinone, and tanshinone IIA were identified and also compared with a reference. Two further antimicrobial zones in the bioautograms were tentatively assigned to be methylenetanshinquinone and tetrahydrotanshinone I (or its structural isomer Methylenedihydrotanshinquinone). In another run, a validation study was performed for the bioquantification of ciprofloxacin and marbofloxacin via HPTLC-Bacillus subtilis. This pointed out the improved quality of the performance that was reached. Cryptotanshinone was biologically quantified in two S. miltiorrhiza root samples. Antimicrobials without an available reference standard were calculated as cryptotanshinone-bioequivalents. The results were of relevance, as 1 ng of cryptotanshinone was calculated to be bioequivalent to 0.6 ng and 2 ng of the synthetic antibiotics, ciprofloxacin and marbofloxacin, respectively. For the first time, quantitative direct bioautography via HPTLC-B. subtilis was shown as a reliable tool for streamlined bioprofiling of complex samples.

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