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Selumetinib

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Primary targets: MEK1, MEK2 · FDA status: FDA Approved

Selectivity scorecard

KISS
100.00
Gini
0.640
CATDS
0.032

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 Selumetinib. Strongest target: MEK1 at 54.4% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1MEK154.4%45.6%
2MEK233.0%67.0%
3SYK29.1%70.9%
4MEKK326.3%73.7%
5CK1A125.8%74.2%
6AKT325.5%74.5%
7ERK124.5%75.5%
8STK3322.7%77.3%
9PRKX20.0%80.0%
10CDK17_CYCLIN_Y(PCTK2)18.6%81.4%
11ALK4_ACVR1B17.9%82.1%
12GLK_MAP4K317.2%82.8%
13TYRO3_SKY17.1%82.9%
14CDK1_CYCLIN_A16.0%84.0%
15MEKK615.9%84.1%
16NEK915.7%84.3%
17EPHA615.7%84.3%
18RAF115.3%84.7%
19AURORA_A15.3%84.7%
20RIPK414.2%85.8%

Selectivity landscape

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

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