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Binimetinib

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

Selectivity scorecard

KISS
100.00
Gini
0.689
CATDS
0.063

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 Binimetinib. Strongest target: MEK1 at 79.1% inhibition.

Accessible data table
RankTargetInhibition %Residual activity %
1MEK179.1%20.9%
2MEK243.5%56.5%
3CDK9_CYCLIN_T133.3%66.7%
4CAMKK223.0%77.0%
5EGFR21.8%78.3%
6ALK3_BMPR1A20.2%79.8%
7TTBK220.0%80.0%
8TGFBR219.7%80.3%
9PDK2_PDHK216.9%83.1%
10MUSK15.4%84.6%
11CAMK2A15.4%84.6%
12LYN15.4%84.6%
13HASPIN14.4%85.6%
14HIPK113.9%86.1%
15VRK213.3%86.7%
16VRK112.5%87.5%
17P38A_MAPK1412.3%87.7%
18STK21_CIT12.2%87.8%
19BRAF12.2%87.8%
20PHKG111.5%88.5%

Selectivity landscape

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

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