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Product introduction
R-268712 是一种口服有效的选择性 ALK-5 抑制剂,其 IC50 值为 2.5 nM。R-268712 能以剂量依赖的方式抑制 Smad3 的磷酸化,其 IC50 值为 10.4 nM。R-268712 通过抑制TGF-β 的信号传导来抑制肾小球肾炎以及肾小球硬化,可用于肾脏纤维化和癌症的研究。 R-268712 is an orally active and selective ALK-5 inhibitor, with an IC50 of 2.5 nM. R-268712 inhibits the phosphorylation of Smad3 in a dose-dependent manner with an IC50 of 10.4 nM. R-268712 suppresses glomerulonephritis as well as glomerulosclerosis by inhibiting TGF-β signaling, which can be used in studies of renal fibrosis and cancer.
Chinese name
R 268712,TGF-βRI抑制剂
English name
R 268712
Chinese alias
4-[2-氟-5-[3-(6-甲基-2-吡啶基)-1H-吡唑-4-基]苯基] -1H-吡唑-1-乙醇
English alias
SCHEMBL5198271 | C20H18FN5O | NCGC00387472-01 | 4-[2-Fluoro-5-[3-(6-methyl-2-pyridinyl)-1H-pyrazol-4-yl]phenyl]-1H-pyrazole-1-ethanol | EX-A2776 | 2-(4-(2-Fluoro-5-(3-(6-methylpyridin-2-yl)-1H-pyrazol-4-yl)phenyl)-1H-pyrazol-1-yl)ethan-1-ol | DTXSID301127
CAS number
879487-87-3
molecular formula
C20H18FN5O
molecular weight
363.39 g/mol
Exact mass
≥98%(HPLC)
PSA
79.600 Ų
Logp
2.200
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R 268712, TGF-βRIinhibitor 100mg

R 268712, TGF-βRIinhibitor 100mg; supplied for laboratory research, analysis, inspection, and scientific procurement use; specifications: 100mg; ≥98%; HPLC.

item number:R286557-100mg
Product model:100mg
level: 100mg; ≥98%; HPLC
Lead Time:30days
sold 805 Items
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Specifications:

100mg

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