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Infigratinib

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Primary targets: FGFR2 · FDA status: FDA Approval Withdrawn

Selectivity scorecard

KISS
98.24
Gini
0.710
CATDS
0.025

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 Infigratinib. Strongest target: FGFR1 at 99.2% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1FGFR199.2%0.8%
2FGFR298.8%1.2%
3FMS98.7%1.3%
4FGFR398.6%1.4%
5FGFR494.7%5.3%
6TAOK2_TAO193.3%6.7%
7DDR191.7%8.3%
8LCK88.0%12.0%
9LYN79.6%20.4%
10C_KIT71.8%28.2%
11FLT4_VEGFR369.4%30.6%
12TIE2_TEK68.9%31.1%
13FLT1_VEGFR167.5%32.5%
14MEKK362.5%37.5%
15EIF2AK261.7%38.3%
16CDK4_CYCLIN_D359.4%40.6%
17YES_YES156.7%43.3%
18TAOK154.7%45.3%
19EIF2AK452.6%47.4%
20NEK251.0%49.0%

Selectivity landscape

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

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