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Dacomitinib

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Primary targets: EGFR · FDA status: FDA Approved

Selectivity scorecard

KISS
97.99
Gini
0.664
CATDS
0.016

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 Dacomitinib. Strongest target: ERBB4_HER4 at 100.0% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1ERBB4_HER4100.0%0.0%
2EGFR99.8%0.2%
3ERBB2_HER299.5%0.5%
4TXK97.9%2.1%
5DDR195.6%4.4%
6BLK94.5%5.5%
7JAK394.4%5.6%
8LYN93.4%6.6%
9LCK88.6%11.4%
10BTK87.2%12.8%
11DDR281.7%18.3%
12ABL180.8%19.2%
13EPHA679.1%20.9%
14C_SRC76.6%23.4%
15PEAK175.2%24.8%
16ITK73.6%26.4%
17FGR72.0%28.0%
18EPHB471.4%28.6%
19LOK_STK1070.2%29.8%
20YES_YES169.7%30.3%

Selectivity landscape

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

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