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XL019

Cat. No. M2566

All AbMole products are for research use only, cannot be used for human consumption.

XL019 Structure
Size Price Availability Quantity
10mM*1mL in DMSO USD 94 In stock
5mg USD 85 In stock
10mg USD 135 In stock
50mg USD 470 In stock
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Quality Control & Documentation
Biological Activity

XL019 is a potent and selective JAK2 inhibitor with IC50 of 2.2 nM, exhibiting >50-fold selectivity over JAK1, JAK3 and TYK2.

Customer Product Validations & Biological Datas
Source Anticancer Res (2017). Figure 2. XL019
Method fluorescence-activated cell sorting analyses
Cell Lines KBV20C cancer cells
Concentrations 5 μM
Incubation Time 24 h
Results As shown in Figure 2A, co-treatment with XL019 and vincristine increased the number of cells arrested in the G2 phase compared to that observed with single treatments with either agent.
Chemical Information
Molecular Weight 444.53
Formula C25H28N6O2
CAS Number 945755-56-6
Solubility (25°C) DMSO 15 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Yu-Yi Chu-Farseeva, et al. Design and synthesis of potent dual inhibitors of JAK2 and HDAC based on fusing the pharmacophores of XL019 and vorinostat

[2] Ji Hyun Cheon, et al. P-gp Inhibition by XL019, a JAK2 Inhibitor, Increases Apoptosis of Vincristine-treated Resistant KBV20C Cells with Increased p21 and pH2AX Expression

[3] Allison Rosenthal, et al. Janus kinase inhibitors for the treatment of myeloproliferative neoplasms

[4] Srdan Verstovsek, et al. Phase I evaluation of XL019, an oral, potent, and selective JAK2 inhibitor

[5] Constantine S Tam, et al. Investigational Janus kinase inhibitors

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Keywords: XL019 supplier, JAK, inhibitors, activators

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