SB525334 , ≥98% , 356559-20-1
Synonym(s):
6-[2-tert-Butyl-5-(6-methyl-pyridin-2-yl)-1H-imidazol-4-yl]-quinoxaline;ALK5 Inhibitor VIII, SB-525334, 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;TGF-β RI Kinase Inhibitor VIII - CAS 356559-20-1 - Calbiochem
Pack Size | Price | Stock | Quantity |
5MG | RMB319.20 | In Stock |
|
10MG | RMB447.20 | In Stock |
|
50MG | RMB1599.20 | In Stock |
|
1G | RMB9599.20 | In Stock |
|
others | Enquire |
PRODUCT Properties
Melting point: | 159 °C |
Boiling point: | 540.5±45.0 °C(Predicted) |
Density | 1.191 |
storage temp. | 2-8°C |
solubility | DMSO: ≥20mg/mL |
pka | 10.24±0.10(Predicted) |
form | Yellow solid |
color | yellow |
Stability: | Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 3 months. |
InChIKey | DKPQHFZUICCZHF-UHFFFAOYSA-N |
Description and Uses
SB-525334 is a potent inhibitor of the TGF-β receptor 1 (TGF-β R1, ALK5) kinase (IC50 = 14.36 nM). It is ~4-fold less effective against ALK4 and inactive against ALK2, ALK3, and ALK6. SB-525334 blocks TGF-β1-induced phosphorylation and nuclear translocation of SMAD2/3 as well as TGF-β1-directed gene expression. It is effective in vivo, preventing puromycin aminonucleoside-induced renal fibrosis and bleomycin-induced pulmonary fibrosis. SB-525334 also modulates carcinogenesis and suppresses the development of pulmonary arterial hypertension in animals.
SB-525334 is a potent activin receptor-like kinase (ALK5)/ type I TGFβ-receptor kinase inhibitor with IC50 = 14.3 nM.
Safety
Symbol(GHS) | GHS06 |
Signal word | Danger |
Hazard statements | H301-H315-H319-H335-H413 |
Precautionary statements | P261-P301+P310-P305+P351+P338 |
Hazard Codes | Xn |
Risk Statements | 22-36/37/38 |
Safety Statements | 26 |
RIDADR | UN 2811 6.1/PG 3 |
WGK Germany | 3 |
HS Code | 2933.39.6190 |