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Nintedanib

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Primary targets: FGFR1, FGFR2, FGFR3 · FDA status: FDA Approved

Selectivity scorecard

KISS
90.23
Gini
0.608
CATDS
0.008

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 Nintedanib. Strongest target: DDR2 at 100.0% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1DDR2100.0%0.0%
2LCK100.0%0.0%
3RET100.0%0.0%
4ABL199.9%0.1%
5MELK99.4%0.6%
6SIK299.4%0.6%
7FLT4_VEGFR399.2%0.8%
8MEK598.6%1.4%
9PDGFRA98.3%1.7%
10BTK98.0%2.0%
11LYN97.9%2.1%
12YES_YES197.9%2.1%
13BLK97.6%2.4%
14FGFR297.0%3.0%
15C_SRC96.9%3.1%
16C_KIT96.8%3.2%
17TRKC96.7%3.3%
18KDR_VEGFR296.4%3.6%
19DDR196.1%3.9%
20PDGFRB96.0%4.0%

Selectivity landscape

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

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