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Cat No.
CEI-0496
Description
A relatively non-toxic Inhibitor of histone deacetylase (HDAC). Facilitates transcriptional activation (TGF-β/Smad4) in both stable and transient receptor assays in a concentration-dependent manner. At ~2 µg/ml (6-8 µM) concentrations, results in a greater than 100-fold increase in histone acetylation in PANC-1 cells.
Appearance
Yellow solid
Product Overview
A HDAC inhibitor
CAS No.
287383-59-9
Molecular Weight
327.33
Purity
>98
Storage
-20 centigrade
Targets
HDAC
Molecular Formula
C 18 H 18 N 2 O 4
Chemical Name
N-Hydroxy-1,3-dioxo-1H-benz[de]isoquinoline-2(3H)-hexanamide
Solubility
DMSO (100 mM)
Shipping Conditions
Gel pack
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