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Pz-1

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Catalog No. T12598Cas No. 1800505-64-9

Pz-1 is an inhibitor of VEGFR2 and RET (rearranged during transfection) tyrosine kinase that blocks the blood supply required for RET-stimulated growth.

Pz-1

Pz-1

🥰Excellent
Purity: 99.95%
Catalog No. T12598Cas No. 1800505-64-9
Pz-1 is an inhibitor of VEGFR2 and RET (rearranged during transfection) tyrosine kinase that blocks the blood supply required for RET-stimulated growth.
Pack SizePriceAvailabilityQuantity
2 mg$30In Stock
5 mg$48In Stock
10 mg$85In Stock
25 mg$172In Stock
50 mg$278In Stock
1 mL x 10 mM (in DMSO)$53In Stock
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Purity:99.95%
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Product Introduction

Bioactivity
Description
Pz-1 is an inhibitor of VEGFR2 and RET (rearranged during transfection) tyrosine kinase that blocks the blood supply required for RET-stimulated growth.
Targets&IC50
RET/VEGFR2:< 1 nM
In vitro
Pz-1(1.0 nM) strongly inhibited phosphorylation of all tested RET oncoproteins in cell-based assays with IC50s of less than 1 nM for both VEGFR2 and RET wild type kinases[1].
In vivo
Pz-1 (1.0 mg/kg) abrogated the formation of tumors induced by RET-mutant fibroblasts and blocked the phosphorylation of both RET and VEGFR2 in tumor tissue. Pz-1 featured no detectable toxicity at concentrations of up to 100.0 mg/kg[1].
Chemical Properties
Molecular Weight454.52
FormulaC26H26N6O2
Cas No.1800505-64-9
SmilesCn1cc(cn1)-c1ccc2n(cnc2c1)-c1ccc(CC(=O)Nc2cc(on2)C(C)(C)C)cc1
Relative Density.1.28 g/cm3 (Predicted)
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
DMSO: 45 mg/mL (99.01 mM), Sonication is recommended.
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.2001 mL11.0006 mL22.0012 mL110.0062 mL
5 mM0.4400 mL2.2001 mL4.4002 mL22.0012 mL
10 mM0.2200 mL1.1001 mL2.2001 mL11.0006 mL
20 mM0.1100 mL0.5500 mL1.1001 mL5.5003 mL
50 mM0.0440 mL0.2200 mL0.4400 mL2.2001 mL

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