XL-228
- Soluble in DMSO
- MF: C22H31N9O
- MW: 437.54
Description
More Information
| Parent CAS No. | 898280-07-4 |
|---|---|
| Chemical Name | N4-(5-cyclopropyl-1H-pyrazol-3-yl)-N2-((3-isopropylisoxazol-5-yl)methyl)-6-(4-methylpiperazin-1-yl)pyrimidine-2,4-diamine |
| extra_info | Sold in collaboration with Chemietek |
| SMILES | C1C(NC2=NNC(C3CC3)=C2)=NC(NCC2=CC(C(C)C)=NO2)=NC=1N1CCN(C)CC1 |
| MFCD | N.A. |
| InChi | InChI=1S/C22H31N9O/c1-14(2)17-10-16(32-29-17)13-23-22-25-19(24-20-11-18(27-28-20)15-4-5-15)12-21(26-22)31-8-6-30(3)7-9-31/h10-12,14-15H,4-9,13H2,1-3H3,(H3,23,24,25,26,27,28) |
| InChiKey | ALKJNCZNEOTEMP-UHFFFAOYSA-N |
| CID | 59757974 |
| Short Description | IGF1R, AURORA kinases, FGFR1-3, ABL, ALK, and SRC inhibitor |
References
- J Cortes et al. Preliminary Clinical Activity in a Phase I Trial of the BCR-ABL/IGF- 1R/Aurora Kinase Inhibitor XL228 in Patients with Ph++ Leukemias with Either Failure to Multiple TKI Therapies or with T315I Mutation. Blood 2008 112:3232.
- O Douglas et al. Abstract C192: Characterization of the target profile of XL228, a multi‐targeted protein kinase inhibitor in phase 1 clinical development. Mol Cancer Ther 2009;8(12 Suppl):C192.
- N Shah et al. Targeting Drug-Resistant CML and Ph+-ALL with the Spectrum Selective Protein Kinase Inhibitor XL228. Blood 2007 110:474.
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