A cell-permeable hydroxyamide-based SAHA analog that potently inhibits histone deacetylase (HDAC) activity (IC50 = 100 nM). Shown to induce histone acetylation and p21 transcription with concomitent inhibition of cell cycle progression in human fibrosarcoma HT1080 cells. Reported to be more potent than SAHA in inhibiting tumor growth in a murine xenograph model in vivo.
|
Product information
|
|
Form
|
White solid
|
|
Molar mass
|
303.4
|
|
Protect from Light
|
Yes
|
|
Packaged under inert gas
|
Yes
|
|
Purity
|
≥95% by HPLC
|
|
Solubility
|
DMSO or MeOH
|
|
Chemical formula
|
C17H21NO2S
|
|
Store and ship information
|
|
|
|
Storage
|
+2°C to +8°C
|
|
Ship
|
Ambient Temperature Only
Irritant
|
|
Safety information
|
|
S Phrase
|
S: 22-24/25-36/37/39
Do not breathe dust.
|
|
R Phrase
|
R: 36/37/38
|