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ALX-350-134 Revised 28-May-08
Pyripyropene A
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SYNONYMS (+)-Pyripyropene A
PPPA
PRODUCT LINE Natural Products / Antibiotics
PRODUCT CATEGORY Other Natural Products
Ordering Information
Product Numbers: Format: Size: Unit Price: Quantity: Add To Cart
ALX-350-134-C500   500 µg 190.00 USD Add To Cart
Product Specification
FORMULA: C31H37NO10
MW: 583.6
CAS NUMBER: 147444-03-9
SOURCE/HOST: Isolated from Aspergillus fumigatus.
PURITY: ≥90% (HPLC)
APPEARANCE: White to off-white powder.
SOLUBILITY: Soluble in methanol or ethyl acetate; insoluble in water or hexane.
SHIPPING: AMBIENT
LONG TERM STORAGE: -20°C

Product Description
Highly specific inhibitor of acyl-coenzyme A:cholesterol acetyltransferase 2 (ACAT2).
Product Specific Literature References
Pyripyropenes, highly potent inhibitors of acyl-CoA:cholesterol acyltransferase produced by Aspergillus fumigatus: S. Omura, et al.; J. Antibiot. 46, 1168 (1993) Abstract
Pyripyropenes, novel inhibitors of acyl-CoA:cholesterol acyltransferase produced by Aspergillus fumigatus. I. Production, isolation, and biological properties: H. Tomoda, et al.; J. Antibiot. 47, 148 (1994) Abstract
Pyripyropenes, novel inhibitors of acyl-CoA:cholesterol acyltransferase produced by Aspergillus fumigatus. II. Structure elucidation of pyripyropenes A, B, C and D: Y.K. Kim, et al.; J. Antibiot. 47, 154 (1994) Abstract
Aflavinines and other antiinsectan metabolites from the ascostromata of Eupenicillium crustaceum and related species: H.J. Wang, et al.; Appl. Environ. Microbiol. 61, 4429 (1995) Abstract; Full Text
Total Synthesis of (+)-Pyripyropene A, a Potent, Orally Bioavailable Inhibitor of
Acyl-CoA:Cholesterol Acyltransferase:
T. Nagamitsu, et al.; J. Org. Chem. 60, 8126 (1995)
Biosynthesis of Pyripyropene A: H. Tomoda, et al.; J. Org. Chem. 61, 882 (1996)
Meroterpenoids with various biological activities produced by fungi: K. Shiomi, et al.; Pure Appl. Chem. 71, 1059 (1999) Full Text
A formal synthesis of (+)-pyripyropene A using a biomimetic epoxy-olefin cyclisation: effect of epoxy alcohol/ether on cyclisation efficiency: V.K. Aggarwal, et al.; J. Chem. Soc. 3315 (1999) Full Text
Mass-production of human ACAT-1 and ACAT-2 to screen isoform-specific inhibitor: a different substrate specificity and inhibitory regulation: K.H. Cho, et al.; BBRC 309, 864 (2003) Abstract
Identification of ACAT1- and ACAT2-specific inhibitors using a novel, cell-based fluorescence assay: individual ACAT uniqueness: A.T. Lada, et al.; J. Lipid Res. 45, 378 (2004) Abstract; Full Text
ACAT2 is localized to hepatocytes and is the major cholesterol-esterifying enzyme in human liver: P. Parini, et al.; Circulation 110, 2017 (2004) Abstract; Full Text
Exploiting PdII and TiIII chemistry to obtain gamma-dioxygenated terpenoids: synthesis of rostratone and novel approaches to aphidicolin and pyripyropene A: J. Justicia, et al.; J. Org. Chem. 70, 8265 (2005) Abstract
Total synthesis of alpha-pyrone meroterpenoids, novel bioactive microbial metabolites: T. Sunazuka and S. Omura; Chem. Rev. 105, 4559 (2005) Abstract
Potential therapeutics for obesity and atherosclerosis: inhibitors of neutral lipid metabolism from microorganisms: H. Tomoda & S. Omura; Pharmacol. Ther. 115, 375 (2007) Abstract
General Information
MANUFACTURER Fungal strain courtesy of The Kitasato Institute, Tokyo.
Further Categories Containing This Product:
Cholesterol & Lipid Transport/Related Products
 
 

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