Online Purchasing Account You are logged on as Guest. LoginRegister a New AccountShopping cart (Empty)
United States 

Asperlactone

Antibiotic
 
ALX-380-122-M001 1 mg 248.00 USD
Do you need bulk/larger quantities?
 
Antibiotic with nematicidal, insecticidal, antibacterial and antifungal activity.

Product Details

Alternative Name:5-(1-Hydroxyethyl)-3-(3-methyloxiranyl)-2(5H)-furanone, 5-(1-Hydroxyethyl)-3-(2,3-epoxypropyl)butenolide
 
Formula:C9H12O4
 
MW:184.2
 
Source:Isolated from Aspergillus ochraceus.
 
CAS:76375-62-7
 
Purity:≥98% (HPLC)
 
Identity:Determined by 1H-NMR.
 
Appearance:Yellow oil.
 
Solubility:Soluble in DMSO, methanol or acetone.
 
Shipping:Blue Ice
 
Short Term Storage:+4°C
 
Long Term Storage:-20°C
 
Use/Stability:Stable for at least 1 year after receipt when stored at -20°C.
 
Handling:After reconstitution protect from light at -20°C.
 
Regulatory Status:RUO - Research Use Only
 
380-122
Please mouse over
380-122

Product Literature References

Characterization and regulation of new secondary metabolites from Aspergillus ochraceus M18 obtained by UV mutagenesis: G. Awad, et al.; Can. J. Microbiol. 51, 59 (2005), Abstract; Full Text
Bactericidal and fungicidal activity of Aspergillus ochraceus metabolites and some derivatives: M. Torres, et al.; Pestic. Sci. 53, 9 (1998),
Aspyrone, a nematicidal compound isolated from the fungus, Aspergillus melleus: Y. Kimura, et al.; Biosci. Biotech. Biochem. 60, 1375 (1996),
Effect of fungal metabolites and some derivatives against Tribolium castaneum (Herbst) and Nezara viridula (L.): M. Balcells, et al.; Pestic. Sci. 45, 319 (1995),
17O NMR in biosynthetic studies: aspyrone, asperlactone and isoasperlactone, metabolites of Aspergillus melleus: J. Staunton & A.C. Sutkowski; J.C.S. Chem. Commun. 1991, 1106 (1991),
Biosynthesis of fungal metabolites: asperlactone and its relationship to other metabolites of Aspergillus melleus: R.G. Brereton, et al.; J.C.S. Perkin Trans. I 1984, 1027 (1984),
New polyketide metabolites from Aspergillus melleus: structural and stereochemical studies: M.J. Garson, et al.; J.C.S. Perkin Trans. I 1984, 1021 (1984),

Product Toolbox

PRODUCT RESOURCES

Datasheet
SDS
Certificate of Analysis

RELATED PRODUCTS

By catalog section:

PRODUCT SUPPORT

FAQs
Technical Service
Customer Service