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Design, synthesis, and biological evaluation of pyrazolo[3,4-d]pyrimidines active in vivo on the Bcr-Abl T315I mutant.
- Source :
-
Journal of medicinal chemistry [J Med Chem] 2013 Jul 11; Vol. 56 (13), pp. 5382-94. Date of Electronic Publication: 2013 Jun 20. - Publication Year :
- 2013
-
Abstract
- Starting from our in-house library of pyrazolo[3,4-d]pyrimidines, a cross-docking simulation was conducted on Bcr-Abl T315I mutant. Among the selected compounds (2a-e), the 4-bromo derivative 2b showed the best activity against the Bcr-Abl T315I mutant. Deeper computational studies highlighted the importance of the bromine atom in the para position of the N1 side chain phenyl ring for the interaction with the T315I mutant. A series of 4-bromo derivatives was thus synthesized and biologically evaluated. Compound 2j showed a good balance of different ADME properties, high activity in cell-free assays, and a submicromolar potency against T315I Bcr-Abl expressing cells. In addition, it was converted into a water-soluble formulation by liposome encapsulation, preserving a good activity on leukemic T315I cells and avoiding the use of DMSO as solubilizing agent. In vivo studies on mice inoculated with 32D-T315I cells and treated with 2j showed a more than 50% reduction in tumor volumes.
- Subjects :
- Animals
Cell Line
Cell Proliferation drug effects
Cells, Cultured
Drug Design
Female
Fusion Proteins, bcr-abl chemistry
Fusion Proteins, bcr-abl genetics
Humans
Mice
Mice, Nude
Models, Chemical
Models, Molecular
Molecular Structure
Neoplasms, Experimental drug therapy
Neoplasms, Experimental genetics
Neoplasms, Experimental pathology
Point Mutation
Protein Binding
Protein Kinase Inhibitors chemical synthesis
Protein Structure, Tertiary
Pyrazoles chemical synthesis
Pyrimidines chemical synthesis
Transfection
Tumor Burden drug effects
Fusion Proteins, bcr-abl antagonists & inhibitors
Protein Kinase Inhibitors pharmacology
Pyrazoles pharmacology
Pyrimidines pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1520-4804
- Volume :
- 56
- Issue :
- 13
- Database :
- MEDLINE
- Journal :
- Journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 23746084
- Full Text :
- https://doi.org/10.1021/jm400233w