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Quizartinib

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Primary targets: FLT3 · FDA status: FDA Approved

Selectivity scorecard

KISS
99.50
Gini
0.737
CATDS
0.038

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 Quizartinib. Strongest target: FLT3 at 97.9% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1FLT397.9%2.1%
2C_KIT97.3%2.7%
3PDGFRB89.0%11.0%
4FMS83.7%16.3%
5RET79.5%20.5%
6MUSK79.2%20.8%
7PDGFRA69.8%30.3%
8TRKB57.6%42.4%
9TRKC53.9%46.1%
10HIPK453.1%46.9%
11RIPK451.4%48.6%
12DDR148.2%51.8%
13ERK7_MAPK1544.3%55.7%
14KHS_MAP4K541.4%58.6%
15TRKA39.4%60.6%
16DDR238.5%61.5%
17FLT4_VEGFR336.3%63.7%
18CAMKK134.7%65.3%
19HGK_MAP4K433.3%66.7%
20MYLK324.5%75.5%

Selectivity landscape

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

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