Ac-CoA Synthase Inhibitor-CAS 508186-14-9-Calbiochem

产品说明

一般描述

A cell-permeable quinoxaline based compound that acts as a potent, reversible inhibitor of acetyl CoA synthetase (ACSS2; IC₅₀ ~ 600 nM in a luciferase based assay). Exhibits selectivity over ACSF2 and ACSL5 acyl-CoA synthetases. Efficiently blocks the uptake of ¹⁴C tracer carbons from acetate into lipids (IC₅₀ = 6.8 µM) and for histone acetylation (IC₅₀ = 5.5 µM) in HepG2 cells.
A cell-permeable quinoxaline based compound that acts as a potent, reversible inhibitor of acetyl CoA synthetase (ACSS2; IC₅₀ ~ 600 nM in a luciferase based assay). Exhibits selectivity over ACSF2 and ACSL5 acyl-CoA synthetases. Efficiently blocks the uptake of ¹⁴C tracer carbons from acetate into lipids (IC₅₀ = 6.8 µM) and for histone acetylation (IC₅₀ = 5.5 µM) in HepG2 cells.

Please note that the molecular weight for this compound is batch-specific due to variable water content. Please refer to the vial label or the certificate of analysis for the batch-specific molecular weight. The molecular weight provided represents the baseline molecular weight without water.

生化/生理作用

Primary Target
ACSS2
Reversible: yes

警告

Toxicity: Standard Handling (A)

重悬

Following reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.

其他说明

Comerford, S.A., et al. 2014. Cell.159, 1591.

法律信息

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

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