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Osimertinib

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Primary targets: EGFR · FDA status: FDA Approved

Selectivity scorecard

KISS
97.24
Gini
0.733
CATDS
0.019

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 Osimertinib. Strongest target: ERBB4_HER4 at 100.0% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1ERBB4_HER4100.0%0.0%
2ERBB2_HER299.4%0.6%
3EGFR99.1%0.9%
4TXK97.6%2.4%
5JAK397.5%2.5%
6ROS_ROS197.2%2.8%
7BTK96.3%3.7%
8TNK192.8%7.2%
9ACK192.6%7.4%
10MYO3B90.9%9.1%
11BLK90.0%9.9%
12MNK186.2%13.8%
13BRK85.8%14.2%
14ITK85.4%14.6%
15LRRK282.4%17.6%
16TNIK81.3%18.7%
17ALK80.5%19.5%
18YSK4_MAP3K1979.7%20.3%
19BMX_ETK79.5%20.5%
20TEC74.6%25.4%

Selectivity landscape

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

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