Methyl tanshinonateCAS# 18887-19-9 |
Quality Control & MSDS
3D structure
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Number of papers citing our products
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Cas No. | 18887-19-9 | SDF | Download SDF |
PubChem ID | 624381 | Appearance | Red powder |
Formula | C20H18O5 | M.Wt | 338.35 |
Type of Compound | Diterpenoids | Storage | Desiccate at -20°C |
Synonyms | Methyltanshinonate;Methuyl Tanshinonate | ||
Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
Chemical Name | methyl 1,6-dimethyl-10,11-dioxo-8,9-dihydro-7H-naphtho[1,2-g][1]benzofuran-6-carboxylate | ||
SMILES | CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C(=O)OC | ||
Standard InChIKey | YFDKIHAZVQFLRC-UHFFFAOYSA-N | ||
Standard InChI | InChI=1S/C20H18O5/c1-10-9-25-18-12-6-7-13-11(15(12)17(22)16(21)14(10)18)5-4-8-20(13,2)19(23)24-3/h6-7,9H,4-5,8H2,1-3H3 | ||
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. |
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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. |
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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. |
Description | 1. Methyl tanshinonate (Methyltanshinonate) has antioxidant activity. 2. Methyl tanshinonate (Methyltanshinonate) can treat psoriasis. 3. Methyl tanshinonate (Methyltanshinonate) has antiatherosclerotic activity. |
Targets | Antifection |
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Methyl tanshinonate Dilution Calculator
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Methyl tanshinonate Molarity Calculator
1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
1 mM | 2.9555 mL | 14.7776 mL | 29.5552 mL | 59.1104 mL | 73.888 mL |
5 mM | 0.5911 mL | 2.9555 mL | 5.911 mL | 11.8221 mL | 14.7776 mL |
10 mM | 0.2956 mL | 1.4778 mL | 2.9555 mL | 5.911 mL | 7.3888 mL |
50 mM | 0.0591 mL | 0.2956 mL | 0.5911 mL | 1.1822 mL | 1.4778 mL |
100 mM | 0.0296 mL | 0.1478 mL | 0.2956 mL | 0.5911 mL | 0.7389 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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Antiplasmodial and antitrypanosomal activity of tanshinone-type diterpenoids from Salvia miltiorrhiza.[Pubmed:21412700]
Planta Med. 2011 Sep;77(14):1594-6.
In a medium throughput screen of 880 plant and fungal extracts for antiprotozoal activity, a dichloromethane extract of Salvia miltiorrhiza roots was active against both Trypanosoma brucei rhodesiense and Plasmodium falciparum. With HPLC-based activity profiling in combination with on- and off-line spectroscopic methods (PDA, -MS (n), HR-MS, microprobe NMR), the active compounds were identified as tanshinone-type diterpenoids. Subsequent isolation and structure elucidation yielded the known substances miltirone (1), tanshinone II a (2), 1,2 dihydrotanshinquinone (3), methylenetanshinquinone (4), 1-oxomiltirone (5), 11-hydroxymiltiodiol (6), tanshinone I (7), methyltanshinonate (8), and cryptotanshinone (9). The IC(5)(0)s of the compounds were determined against the two parasites and rat myoblast (L6) cells. They ranged from 4.1 microM to over 30 microM against P. falciparum K1 strain with selectivity indices (SI) from 0.3 to 1.9. IC(5)(0)s against T. brucei rhodesiense STIB 900 were from 0.5 microM (1, 4) to over 30 microM, and 4 showed the greatest selective activity with an SI of 24.