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Erdafitinib

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Primary targets: FGFR1 · FDA status: FDA Approved

Selectivity scorecard

KISS
95.71
Gini
0.737
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 Erdafitinib. Strongest target: FGFR3 at 99.1% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1FGFR399.1%0.9%
2FGFR299.0%1.0%
3FGFR199.0%1.0%
4FGFR498.0%2.0%
5C_KIT98.0%2.0%
6FLT4_VEGFR397.9%2.1%
7LYN97.8%2.2%
8FMS97.6%2.4%
9EIF2AK297.0%3.0%
10FLT1_VEGFR196.6%3.4%
11DDR195.8%4.2%
12RET94.7%5.3%
13PDGFRA94.5%5.5%
14DDR293.5%6.5%
15KDR_VEGFR291.8%8.2%
16LCK91.7%8.3%
17ABL190.9%9.1%
18EPHB489.7%10.3%
19EPHB189.3%10.7%
20EPHA587.6%12.4%

Selectivity landscape

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

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