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Documentos Principais

G5547

Sigma-Aldrich

GSK837149A

≥98% (HPLC), solid

Sinônimo(s):

N,N′-Di[4-(4-Methyl-pyrimidin-2-ylsulfamoyl)phenyl]-urea

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5 MG
R$ 1.230,00

R$ 1.230,00


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5 MG
R$ 1.230,00

About This Item

Fórmula empírica (Notação de Hill):
C23H22N8O5S2
Número CAS:
Peso molecular:
554.60
Número MDL:
Código UNSPSC:
51111800
NACRES:
NA.77

R$ 1.230,00


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Nível de qualidade

Ensaio

≥98% (HPLC)

Formulário

solid

cor

white to off-white

solubilidade

DMSO: >10 mg/mL
H2O: insoluble

originador

GlaxoSmithKline

temperatura de armazenamento

2-8°C

Ações bioquímicas/fisiológicas

GSK837149A is a selective inhibitor of human fatty acid synthase (FAS).
GSK837149A is the first selective inhibitor of human fatty acid synthase (FAS) known to act specifically and selectively on the KR activity of the enzyme. It was first isolated as a minor impurity in a sample found to be active against the enzyme in a high-throughput screening campaign. This compound and its analogs synthesized, all being symmetrical structures containing a bisulfonamide urea, act by inhibiting the beta-ketoacyl reductase activity of the enzyme. GSK837149A inhibits FAS in a reversible mode, with a Ki value of approximately 30 nm, and it possibly binds to the enzyme-ketoacyl-ACP complex. Although initial results suggest that cell penetration for these compounds is impaired, they still can be regarded as useful tools with which to probe and explore the beta-ketoacyl reductase active site in FAS, helping in the design of new inhibitors.

Características e benefícios

This compound was developed by GlaxoSmithKline. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

Pictogramas

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Palavra indicadora

Warning

Frases de perigo

Classificações de perigo

Eye Irrit. 2

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves


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Sigma-Aldrich

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Human cancers require fatty acid synthase (FASN)-dependent de novo long-chain fatty acid synthesis for proliferation. FASN is therefore an attractive drug target, but fast technologies for reliable label-free cellular compound profiling are lacking. Recently, MALDI-mass spectrometry (MALDI-MS) has emerged as

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