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PD-161570

Cat. No. M8043

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PD-161570 Structure
Synonym:

PD161570

Size Price Availability Quantity
5mg USD 100 In stock
10mg USD 160 In stock
25mg USD 325 In stock
50mg USD 515 In stock
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Quality Control & Documentation
Biological Activity

PD-161570 is a potent and ATP-competitive human FGF-1 receptor inhibitor with an IC50 of 39.9 nM and a Ki of 42 nM. PD-161570 inhibits PDGF-stimulated autophosphorylation and FGF-1 receptor phosphorylation with IC50s of 450 nM and 622 nM, respectively. PD-161570 is also a bone morphogenetic proteins (BMPs) and TGF-β signaling inhibitor. PD-161570 also inhibits the PDGFR, EGFR and c-Src tyrosine kinases with IC50 values of 310 nM, 240 nM, and 44 nM, respectively.

Chemical Information
Molecular Weight 532.51
Formula C26H35Cl2N7O
CAS Number 192705-80-9
Solubility (25°C) DMSO 29 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Kyosuke Hino, et al. An mTOR Signaling Modulator Suppressed Heterotopic Ossification of Fibrodysplasia Ossificans Progressiva

[2] Ashley Wolfe, et al. Pharmacologic characterization of a kinetic in vitro human co-culture angiogenesis model using clinically relevant compounds

[3] Seema Saksena, et al. Keratinocyte growth factor-2 stimulates P-glycoprotein expression and function in intestinal epithelial cells

[4] David A Stevens, et al. Thyroid hormone activates fibroblast growth factor receptor-1 in bone

[5] B L Batley, et al. Inhibition of FGF-1 receptor tyrosine kinase activity by PD 161570, a new protein-tyrosine kinase inhibitor

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  Catalog
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Keywords: PD-161570, PD161570 supplier, FGFR, inhibitors, activators

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