Marilactone

CAS# 34818-17-2

Marilactone

2D Structure

Catalog No. BCN7363----Order now to get a substantial discount!

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Marilactone: 5mg $615 In Stock
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Quality Control of Marilactone

3D structure

Package In Stock

Marilactone

Number of papers citing our products

Chemical Properties of Marilactone

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.
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 Marilactone

The metabolites of the fungus Stachylidium sp.

Biological Activity of Marilactone

DescriptionMarilactone is a natural product from the fungus Stachylidium sp.

Protocol of Marilactone

Structure Identification
J Nat Prod. 2013 Mar 22;76(3):322-6.

Unprecedented polyketides from a marine sponge-associated Stachylidium sp.[Pubmed: 23268694 ]


METHODS AND RESULTS:
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.
CONCLUSIONS:
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).

Marilactone Dilution Calculator

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Marilactone Molarity Calculator

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Preparing Stock Solutions of Marilactone

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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References on Marilactone

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).

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