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Lorlatinib

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Primary targets: ALK · FDA status: FDA Approved

Selectivity scorecard

KISS
97.24
Gini
0.694
CATDS
0.018

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 Lorlatinib. Strongest target: ROS_ROS1 at 99.5% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1ROS_ROS199.5%0.5%
2ACK199.3%0.7%
3FER98.1%1.9%
4FAK_PTK297.7%2.3%
5PYK297.6%2.4%
6ALK97.2%2.8%
7TYK1_LTK93.8%6.2%
8FES_FPS93.7%6.3%
9GRK792.0%8.0%
10TRKC91.3%8.7%
11TRKB90.5%9.5%
12PHKG288.5%11.5%
13TNK187.9%12.1%
14STK22D_TSSK186.4%13.6%
15NEK881.2%18.8%
16PLK4_SAK80.6%19.4%
17FRK_PTK580.0%20.0%
18CAMKK279.2%20.8%
19DCAMKL177.5%22.5%
20SLK_STK273.0%27.0%

Selectivity landscape

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

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