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Crizotinib

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Primary targets: ALK, ROS_ROS1 · FDA status: FDA Approved

Selectivity scorecard

KISS
91.39
Gini
0.581
CATDS
0.009

Computed from wild-type kinome inhibition at 1 μM. Gini reproduces the published values within tolerance; KISS and CATDS are computed but pending reconciliation with the paper's reference code.

Polypharmacology radar

Top 20 strongest-inhibited wild-type kinases for Crizotinib. Strongest target: EPHA6 at 100.0% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1EPHA6100.0%0.0%
2ROS_ROS1100.0%0.0%
3RON_MST1R99.8%0.2%
4LIMK198.9%1.1%
5JAK298.7%1.3%
6TRKB98.5%1.5%
7TYK1_LTK98.3%1.7%
8HPK1_MAP4K197.9%2.1%
9ALK97.7%2.3%
10MUSK97.7%2.3%
11TRKC97.3%2.7%
12AXL97.1%2.9%
13ABL197.0%3.0%
14LCK96.8%3.2%
15EPHB196.8%3.2%
16C_MET96.7%3.3%
17ARK5_NUAK196.4%3.6%
18EPHA296.0%4.0%
19TRKA95.8%4.2%
20FAK_PTK295.7%4.3%

Selectivity landscape

Where Crizotinib sits in the 92-drug selectivity landscape (KISS vs Gini). The highlighted point is Crizotinib.

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