<p>A: Biochemical components of kinase inhibitors that contribute to the specific targeting of <i>ABL1</i> dependent cell growth. The circle labelled ABL1 refers to biochemical ABL1 inhibition. B: Inhibitors with equal ABL1 and ABL2 affinity in an independent dataset <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0092146#pone.0092146-Davis1" target="_blank">[12]</a> are better in targeting <i>ABL1</i>-dependent cell growth than inhibitors with ABL1 activity alone. Poor ABL2 affinity signifies binding K<sub>d</sub> differences between 4 and 26-fold compared to ABL1. Equal affinity signifies binding K<sub>d</sub> differences between 0.5 and 4-fold.</p
Abl kinase inhibitors targeting the ATP binding pocket are currently used as a front-line therapy fo...
Chemoproteomics profiling of kinase inhibitors with kinobeads enables the assessment of inhibitor po...
The c-Abl protein-tyrosine kinase regulates diverse cellular signaling pathways involved in cell gro...
The anti-proliferative activities of all twenty-five targeted kinase inhibitor drugs that are in cli...
Quantifying binding specificity and drug resistance of protein kinase inhibitors is of funda-mental ...
Drug discovery programs frequently target members of the human kinome and try to identify small mole...
Because of the success of imatinib, the first type-II kinase inhibitor approved by the FDA in 2001, ...
<p>(A) Some 200 human kinases were individually ranked according to their enzymatic inhibition by K0...
<p>A: Hierarchical clustering of inhibitory profiles of all kinase drugs in a panel of more than 300...
<p>Each circle represents a marketed kinase inhibitor and its targeted cell growth inhibition. A: Ce...
SummarySmall-molecule inhibitors of protein and lipid kinases have emerged as indispensable tools fo...
Abl kinases are prototypic cytoplasmic tyrosine kinases and are involved in a variety of chromosomal...
Chemoproteomics profiling of kinase inhibitors with kinobeads enables the assessment of inhibitor po...
Identifying selective kinase inhibitors remains a major challenge. The design of bivalent inhibitors...
Chemoproteomics profiling of kinase inhibitors with kinobeads enables the assessment of inhibitor po...
Abl kinase inhibitors targeting the ATP binding pocket are currently used as a front-line therapy fo...
Chemoproteomics profiling of kinase inhibitors with kinobeads enables the assessment of inhibitor po...
The c-Abl protein-tyrosine kinase regulates diverse cellular signaling pathways involved in cell gro...
The anti-proliferative activities of all twenty-five targeted kinase inhibitor drugs that are in cli...
Quantifying binding specificity and drug resistance of protein kinase inhibitors is of funda-mental ...
Drug discovery programs frequently target members of the human kinome and try to identify small mole...
Because of the success of imatinib, the first type-II kinase inhibitor approved by the FDA in 2001, ...
<p>(A) Some 200 human kinases were individually ranked according to their enzymatic inhibition by K0...
<p>A: Hierarchical clustering of inhibitory profiles of all kinase drugs in a panel of more than 300...
<p>Each circle represents a marketed kinase inhibitor and its targeted cell growth inhibition. A: Ce...
SummarySmall-molecule inhibitors of protein and lipid kinases have emerged as indispensable tools fo...
Abl kinases are prototypic cytoplasmic tyrosine kinases and are involved in a variety of chromosomal...
Chemoproteomics profiling of kinase inhibitors with kinobeads enables the assessment of inhibitor po...
Identifying selective kinase inhibitors remains a major challenge. The design of bivalent inhibitors...
Chemoproteomics profiling of kinase inhibitors with kinobeads enables the assessment of inhibitor po...
Abl kinase inhibitors targeting the ATP binding pocket are currently used as a front-line therapy fo...
Chemoproteomics profiling of kinase inhibitors with kinobeads enables the assessment of inhibitor po...
The c-Abl protein-tyrosine kinase regulates diverse cellular signaling pathways involved in cell gro...