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Fedratinib

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Primary targets: JAK2 · FDA status: FDA Approved

Selectivity scorecard

KISS
96.21
Gini
0.576
CATDS
0.010

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 Fedratinib. Strongest target: RET at 99.9% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1RET99.9%0.1%
2JAK299.4%0.6%
3FLT398.2%1.8%
4ZIPK_DAPK397.7%2.3%
5DAPK197.3%2.6%
6SIK296.8%3.2%
7DDR195.2%4.8%
8FAK_PTK294.4%5.6%
9JAK194.2%5.8%
10TYK293.6%6.4%
11ARK5_NUAK193.5%6.5%
12ACK193.4%6.6%
13AURORA_C92.1%7.9%
14ROS_ROS190.7%9.3%
15STK22D_TSSK190.5%9.5%
16SIK188.8%11.2%
17FLT4_VEGFR388.4%11.6%
18DDR288.3%11.7%
19LCK87.1%12.9%
20YES_YES186.8%13.2%

Selectivity landscape

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

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