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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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Project Description:

For research and industrial use only, not for personal medicinal use.

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