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Ceritinib

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Primary targets: ALK · FDA status: FDA Approved

Selectivity scorecard

KISS
95.44
Gini
0.618
CATDS
0.014

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 Ceritinib. Strongest target: FES_FPS at 99.8% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1FES_FPS99.8%0.3%
2STK22D_TSSK199.7%0.3%
3LRRK299.4%0.6%
4IRR_INSRR98.9%1.1%
5FER98.4%1.6%
6ALK98.3%1.7%
7IGF1R98.1%1.9%
8IR97.8%2.2%
9ROS_ROS197.7%2.3%
10TNK197.3%2.7%
11TYK1_LTK97.3%2.7%
12ACK197.2%2.8%
13FAK_PTK296.4%3.6%
14MYO3B94.4%5.6%
15CAMKK292.7%7.3%
16CLK192.1%7.9%
17CLK291.1%8.9%
18PHKG190.1%9.9%
19PYK289.7%10.3%
20STK32B_YANK289.3%10.7%

Selectivity landscape

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

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