A non-cytotoxic inhibitor of ACC and fatty acid synthesis
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TOFA

Item No. 10005263

Technical Information
Formal Name
5-(tetradecyloxy)-2-furancarboxylic acid
CAS Number
54857-86-2
Synonyms
  • RMI 14514
  • 5-(Tetradecyloxy)-2-furoic Acid
Molecular Formula
C19H32O4
Formula Weight
Purity
≥98%
Formulation
A crystalline solid
DMF: 10 mg/mlDMF:PBS (pH 7.2) (1:1): .5 mg/mlDMSO: 2 mg/mlEthanol: 1 mg/ml
λmax
278 nm
SMILES
CCCCCCCCCCCCCCOc1ccc(o1)C(=O)O
InChi Code
InChI=1S/C19H32O4/c1-2-3-4-5-6-7-8-9-10-11-12-13-16-22-18-15-14-17(23-18)19(20)21/h14-15H,2-13,16H2,1H3,(H,20,21)
InChi Key
CZRCFAOMWRAFIC-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    OBESITY RESEARCH SOLUTIONS
    Product Description

    TOFA is an inhibitor of fatty acid synthesis blocking the synthesis of malonyl-CoA by acetyl-CoA carboxylase (ACC).1 Both cerulenin (at about 10 µg/ml) and TOFA (at about 1 µg/ml) are effective at blocking the incorporation of radiolabeled acetate into palmitate. However, TOFA reduces malonyl-CoA levels rather than elevating them, and TOFA is relatively non-toxic to various cancer cell lines. TOFA also attenuates the inhibition of feeding observed when FASN inhibitors such as cerulenin and C75 are administered to obese ob/ob mice.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Loftus, T.M., Jaworsky, D.E., Frehywot, G.L., et alReduced food intake and body weight in mice treated with fatty acid synthase inhibitors. Science 288(5475), 2379-2381 (2000).

    Product Citations

    Desseaux, V., Koukiekolo, R., Moreau, Y., et alMechanism of porcine pancreatic α-amylase: Inhibition of amylose and maltopentaose hydrolysis by various inhibitors. Biologia 57(Suppl 11), 163-170 (2002).