MarilactoneCAS# 34818-17-2 |
Quality Control & MSDS
Number of papers citing our products
Chemical structure
3D structure
| Cas No. | 34818-17-2 | SDF | Download SDF |
| PubChem ID | 54719445 | Appearance | Powder |
| Formula | C8H10O3 | M.Wt | 154.16 |
| Type of Compound | Phenols | Storage | Desiccate at -20°C |
| Solubility | Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc. | ||
| Chemical Name | 6-ethyl-4-hydroxy-3-methylpyran-2-one | ||
| SMILES | CCC1=CC(=C(C(=O)O1)C)O | ||
| Standard InChIKey | USMZMYPGRVEPNO-UHFFFAOYSA-N | ||
| Standard InChI | InChI=1S/C8H10O3/c1-3-6-4-7(9)5(2)8(10)11-6/h4,9H,3H2,1-2H3 | ||
| 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. |
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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 | Marilactone is a natural product from the fungus Stachylidium sp. |
| Structure Identification | J Nat Prod. 2013 Mar 22;76(3):322-6.Unprecedented polyketides from a marine sponge-associated Stachylidium sp.[Pubmed: 23268694 ]
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Marilactone Dilution Calculator
Marilactone Molarity Calculator
| 1 mg | 5 mg | 10 mg | 20 mg | 25 mg | |
| 1 mM | 6.4868 mL | 32.4338 mL | 64.8677 mL | 129.7353 mL | 162.1692 mL |
| 5 mM | 1.2974 mL | 6.4868 mL | 12.9735 mL | 25.9471 mL | 32.4338 mL |
| 10 mM | 0.6487 mL | 3.2434 mL | 6.4868 mL | 12.9735 mL | 16.2169 mL |
| 50 mM | 0.1297 mL | 0.6487 mL | 1.2974 mL | 2.5947 mL | 3.2434 mL |
| 100 mM | 0.0649 mL | 0.3243 mL | 0.6487 mL | 1.2974 mL | 1.6217 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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Unprecedented polyketides from a marine sponge-associated Stachylidium sp.[Pubmed:23268694]
J Nat Prod. 2013 Mar 22;76(3):322-6.
From the marine sponge-derived fungus Stachylidium sp. six novel phthalide-related compounds, cyclomarinone (1), maristachones A-E (2-5), and Marilactone (6), were isolated. The structure of compound 1 comprises a hydroxycyclopentenone ring instead of the furanone ring characteristic for phthalides and represents a new carbon arrangement within polyketides. In the epimeric compounds 5a and 5b the phthalide (=isobenzofuranone) nucleus is modified to an isobenzofuran ring with ketal and acetal functionalities. Biosynthetically the structural skeletons of cyclomarinone (1) and maristachones A (2), C (4), D (5a), and E (5b) are most unusual due to the presence of an additional carbon atom when compared to the basic polyketide skeleton. This special biosynthetic feature also holds true for the likewise isolated polyketide Marilactone (6).
