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613450

TOFA

≥98% (HPLC), Acetyl-CoA carboxylase inhibitor, solid

Sinónimos:

TOFA, 5-(Tetradecyloxy)-2-furoic acid

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A ustedes/SKUDisponibilidadPrecio
5 mg

Disponible para enviar HOYdesdeMerck Chemicals and LS SA

383,00 €

Acerca de este artículo

Fórmula empírica (notación de Hill):
C19H32O4
Número CAS:
Peso molecular:
324.45
UNSPSC Code:
41121800
NACRES:
NA.77
MDL number:
Assay:
≥98% (HPLC)
Form:
solid
Storage condition:
OK to freeze, protect from light

383,00 €


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Nombre del producto

TOFA, A cell-permeable furoic acid compound that acts as a potent, reversible, and competitive inhibitor of acetyl-CoA carboxylase (ACC), a key enzyme involved in the fatty acid biosynthesis.

Quality Segment

assay

≥98% (HPLC)

form

solid

manufacturer/tradename

Calbiochem®

storage condition

OK to freeze, protect from light

color

off-white

solubility

DMSO: 10 mg/mL, ethanol: 5 mg/mL

shipped in

ambient

storage temp.

2-8°C

SMILES string

[o]1c(ccc1C(=O)O)OCCCCCCCCCCCCCC

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

General description

A cell-permeable furoic acid compound that acts as a potent, reversible, and competitive inhibitor of acetyl-CoA carboxylase (ACC), a key enzyme involved in the fatty acid biosynthesis. Inhibits cellular fatty acid synthesis in a dose-dependent manner (IC50 = 4 µM in human breast cancer cell line MCF7). TOFA-induced reduction in malonyl-CoA is reported to off-set the effect of C75 (Cat. No. 341325) on food intake in fasted mice and on apoptosis in tumor cells.
A cell-permeable, potent, reversible, and competitive inhibitor of acetyl-CoA carboxylase (ACC), a key enzyme involved in fatty acid biosynthesis. Inhibits cellular fatty acid synthesis in a dose-dependent manner (IC50 = 4 µM in human breast cancer cell line MCF7). TOFA-induced reduction in malonyl-CoA is reported to off-set the effects of C75 (Cat. No. 341325) on food intake in fasted mice and on apoptosis in tumor cells.

Biochem/physiol Actions

Cell permeable: yes
Primary Target
Acetyl-CoA carboxylase (ACC)
Product competes with ATP.
Reversible: yes
Target IC50: 4 µM inhibiting cellular fatty acid synthesis in human breast cancer cell line MCF7

Packaging

Packaged under inert gas

Preparation Note

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Slight warming and sonication may be required for complete solubilization in ethanol.

Other Notes

Landree, L.E., et al. 2004. J. Biol. Chem.279, 3817.
Zhou, W., et al. 2003. Cancer Res.63, 7330.
Hu, Z., et al. 2003. Proc. Natl. Acad. Sci. USA100, 12624.
Pizer, E.S., et al. 2000. Cancer Res.60, 213.
Arbeeny, C.M., et al. 1992. J. Lipid Res.33, 843.
Fukuda, N. and Ontko, J.A. 1984. J. Lipid Res.25, 831.

Legal Information

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Toxicity: Carcinogenic / Teratogenic (D)

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Este artículo
T6575900518T27006
description

A cell-permeable furoic acid compound that acts as a potent, reversible, and competitive inhibitor of acetyl-CoA carboxylase (ACC), a key enzyme involved in the fatty acid biosynthesis.

description

≥98% (HPLC)

description

anhydrous, ZerO2®, ≥99.0%

description

99%

assay

≥98% (HPLC)

assay

≥98% (HPLC)

assay

≥99.0%

assay

99%

form

solid

form

powder

form

liquid

form

-

Quality Level

100

Quality Level

200

Quality Level

100

Quality Level

200

manufacturer/tradename

Calbiochem®

manufacturer/tradename

-

manufacturer/tradename

-

manufacturer/tradename

-

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

-

storage temp.

2-8°C

solubility

ethanol: 5 mg/mL, DMSO: 10 mg/mL

solubility

DMSO: 2 mg/mL, clear

solubility

-

solubility

-


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Clase de almacenamiento

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable



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