Marilactone | CAS:34818-17-2 | Manufacturer ChemFaces

Marilactone

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Size /Price /Stock	10 mM * 1 mL in DMSO / Inquiry
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Marilactone Description

Source:	The metabolites of the fungus Stachylidium sp.
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Storage:	Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C). Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com
After receiving:	The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.

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).

Product Name	Marilactone
Price:
CAS No.:	34818-17-2
Catalog No.:	CFN89069
Molecular Formula:	C₈H₁₀O₃
Molecular Weight:	154.16 g/mol
Purity:	>=98%
Type of Compound:	Phenols
Physical Desc.:	Powder
Source:	The metabolites of the fungus Stachylidium sp.
Solvent:	Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Download:	COA MSDS
Similar structural:	Comparison
Guestbook:

Size /Price /Stock	10 mM * 100 uL in DMSO / Inquiry / In-stock 10 mM * 1 mL in DMSO / Inquiry / In-stock
Related Libraries	Phenols Compound Library

	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

CFN96352	Longipedlactone J	1011762-93-8	536.7	C₃₂H₄₀O₇
CFN92874	Yuexiandajisu D	866556-15-2	350.4	C₂₀H₃₀O₅
CFN99664	Ehretioside B	156368-84-2	311.3	C₁₄H₁₇NO₇
CFN98247	Rivulobirin E	237407-59-9	590.6	C₃₂H₃₀O₁₁