Product Details
Place of Origin: China
Brand Name: Sunshine
Certification: ISO,COA
Model Number: 20350-15-6
Payment & Shipping Terms
Minimum Order Quantity: Negotiation
Price: Negotiation
Packaging Details: Bag,Drum
Delivery Time: 7-15 days
Payment Terms: L/C, D/A, T/T, Western Union
Supply Ability: TON
CAS NO:: |
20350-15-6 |
Appearance:: |
White Solid |
Molecular Formula:: |
C16H24O4 |
Molecular Weight:: |
280.35900 |
EINECS NO:: |
606-528-3 |
MDL NO:: |
MFCD00083258 |
CAS NO:: |
20350-15-6 |
Appearance:: |
White Solid |
Molecular Formula:: |
C16H24O4 |
Molecular Weight:: |
280.35900 |
EINECS NO:: |
606-528-3 |
MDL NO:: |
MFCD00083258 |
Product Description:
Product Name: Brefeldin A CAS NO: 20350-15-6
Synonyms:
(1R,2E,6S,10E,11aS,13S,14aR)-1,13-dihydroxy-6-Methyl-6,7,8,9,12,13,14,14a-octahydro-1H-cyclopenta[f][1]oxacyclotridecin-4(11aH)-one;
Ascotoxin, Cyanein, DecuMbin;
Brefeldin A, FroM EupenicilliuM brefeldianuM;
Chemical & Physical Properties:
Appearance: White solid
Assay :≥99.0%
Density: 1.108 g/cm3
Boiling Point: 492.7℃ at 760 mmHg
Melting Point: 200-205℃
Flash Point: 87℃
Refractive Index: 1.513
Storage Condition: 2-8℃
Vapor Pressure: 0mmHg at 25℃
Water Solubility: Soluble in dimethylsulfoxide, dichloromethane and ethanol. Slightly soluble in water.
Safety Information:
RTECS: GY8410000
Safety Statements: S24/25; S45; S36; S26
WGK Germany: 3
RIDADR: UN 2811 6
Risk Statement: R25
Hazard Codes: Xn; T
Brefeldin A is a lactone antibiotic produced by fungal organisms such as Eupenicillium brefeldianum. Brefeldin A inhibits protein transport from the endoplasmic reticulum to the Golgi apparatus indirectly by preventing formation of COPI-mediated transport vesicles. Brefeldin A was initially isolated as an anti-viral antibiotic but is now primarily used in biological research to study protein transport. Brefeldin A is a potent inhibitor of cell growth first described in 1958, then independently rediscovered by several groups as a potent active in a broad range of bioassays. Brefeldin has antiviral, antibiotic, antifungal, antitumour and herbicidal activity. Early studies on the mode of action of brefeldin identified inhibition of protein and nucleic acid synthesis by disruption of the Golgi apparatus. The precise molecular target is a subset of Sec7-type GTP exchange factors (GEFs) that activate a small GTPase, Arf1p, an integral component of protein trafficking and signalling.
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