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616459  TGF-β RI Kinase Inhibitor VIII

6-(2-tert-Butyl-5-(6-methyl-pyridin-2-yl)-1H-imidazol-4-yl)-quinoxaline, Transforming Growth Factor-β Type I Receptor Kinase Inhibitor VIII, SB-525334, ALK5 Inhibitor VIII

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09 February 2012

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616459-2MG  2 mg 
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A cell-permeable quinoxaline compound that acts as a potent, highly selective, ATP-competitive inhibitor against type I TGF-β receptor TβR-I/ALK5 (IC50 = 14.3 nM), while exhibiting 4-fold less potency toward ALK4 (IC50 = 58.5 nM) and little or no activity against ALK2/3/6 and a panel of 26 other commonly studied kinases (≤29% inhibition at 10 µM). Effectively blocks (by >95%) TGF-β1-induced Smad2/3 activation (2 µM in ELT-3 cultures) and nuclear localization (1 µM in RPTE cultures), as well as TGF-β1-dependent p3TP- and ARE-luciferase transcription (0.1 µM in HaCat cultures). SB-525334 is orally available and is shown to attenuate Bleomycin- and Puromycin-induced tissue fibrosis in mice and rats in vivo.
Product information
Form Yellow solid
Molar mass 343.4
Protect from Light Yes
Packaged under inert gas Yes
Purity ≥97% by HPLC
Solubility DMSO
Chemical formula C21H21N5
CAS number 356559-20-1
Store and ship information

Hazardous Materials Attention: Due to the nature of the Hazardous Materials in this shipment, additional shipping chargesmay be applied to your order. Certain sizes may be exempt from the additional hazardous materials shipping charges. Please contact your local sales office for more information regarding these charges.

Storage +2°C to +8°C
Ship Ambient Temperature Only
Harmful
Safety information
S Phrase S: 26

In case of contact with eyes, rinse immediately with plenty of water and seek medical advice.
R Phrase R: 22-36/37/38

Harmful if swallowed.
Irritating to eyes, respiratory system and skin.
TGF-β RI Kinase Inhibitor VIII, molecular structure

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© Merck KGaA, Darmstadt, Germany, 2012

All references to Merck refer to Merck KGaA, Darmstadt, Germany.

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