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Midostaurin

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Primary targets: FLT3 · FDA status: FDA Approved

Selectivity scorecard

KISS
78.64
Gini
0.500
CATDS
0.006

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 Midostaurin. Strongest target: JAK3 at 100.0% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1JAK3100.0%0.0%
2MST2_STK3100.0%0.0%
3PHKG1100.0%0.0%
4GLK_MAP4K399.4%0.6%
5MLK3_MAP3K1199.2%0.8%
6CAMK2D98.9%1.1%
7JAK298.9%1.1%
8SIK298.8%1.2%
9FLT398.6%1.4%
10RSK398.5%1.5%
11PKN1_PRK198.5%1.5%
12AURORA_A98.4%1.6%
13ARK5_NUAK198.3%1.7%
14MLK1_MAP3K998.0%2.0%
15YSK4_MAP3K1997.9%2.1%
16MARK497.9%2.1%
17MST1_STK497.4%2.6%
18MARK397.4%2.6%
19AMPK(A1_B2_G2)97.3%2.7%
20FMS97.3%2.7%

Selectivity landscape

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

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